{"id":110,"date":"2014-06-07T16:21:31","date_gmt":"2014-06-07T16:21:31","guid":{"rendered":"http:\/\/jkang.faculty.unlv.edu\/?page_id=110"},"modified":"2026-08-05T14:45:07","modified_gmt":"2026-08-05T14:45:07","slug":"publication","status":"publish","type":"page","link":"https:\/\/jkang.faculty.unlv.edu\/?page_id=110","title":{"rendered":"Publication \/ Patent"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>2026<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\" id=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.6c02541\">44) Bhowmik, S.; Odoh, S. O.; Kang, J. Y. &#8220;Hydropersulfide-Mediated Stereoselective and Regioselective Hydrothiolation of P-alkynes&#8221; <em>Organic Letters <\/em><strong>2026<\/strong>, 28, 9371-9376. DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.6c02541\" data-type=\"link\" data-id=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.6c02541\">10.1021\/acs.orglett.6c02541<\/a>.<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><a href=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/images_medium_ol6c02541_0010.webp\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"210\" src=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/images_medium_ol6c02541_0010.webp\" alt=\"\" class=\"wp-image-842\" style=\"width:365px;height:auto\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/images_medium_ol6c02541_0010.webp 500w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/images_medium_ol6c02541_0010-300x126.webp 300w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\" id=\"https:\/\/pubs.rsc.org\/ra\/article\/doi\/10.1039\/d6ra03773a\/1273822\/A-concise-synthesis-of-alkyl-aryl-hydropersulfides\">43) Bhowmik, S.; Kang, J. Y. &#8220;A concise synthesis of alkyl, aryl hydropersulfides&#8221; <br><em>RSC Advances <\/em><strong>2026<\/strong>, 16, 37522-37526. DOI: <a href=\"https:\/\/pubs.rsc.org\/ra\/article\/doi\/10.1039\/d6ra03773a\/1273822\/A-concise-synthesis-of-alkyl-aryl-hydropersulfides\" data-type=\"link\" data-id=\"https:\/\/pubs.rsc.org\/ra\/article\/doi\/10.1039\/d6ra03773a\/1273822\/A-concise-synthesis-of-alkyl-aryl-hydropersulfides\">10.1039\/d6ra03773a<\/a>\u00a0<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><a href=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/m_d6ra03773a-ga.png\"><img loading=\"lazy\" decoding=\"async\" width=\"520\" height=\"209\" src=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/m_d6ra03773a-ga.png\" alt=\"\" class=\"wp-image-841\" style=\"width:364px;height:auto\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/m_d6ra03773a-ga.png 520w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2026\/07\/m_d6ra03773a-ga-300x121.png 300w\" sizes=\"auto, (max-width: 520px) 100vw, 520px\" \/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>2025<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">42) Ash, J.; Curtis, K.; Bhowmik, S.; Odoh, S. O.; Kang, J. Y. &#8220;Hydropersulfide (RSSH)-Mediated Hydrothiolation of Alkenes&#8221; <em>J. Org. Chem.<\/em>, <strong>2025<\/strong>, <em>90<\/em>, 1167-1174 <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.4c02309\">https:\/\/doi.org\/10.1021\/acs.joc.4c02309<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><a href=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM.png\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"456\" src=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM-1024x456.png\" alt=\"\" class=\"wp-image-832\" style=\"width:376px;height:auto\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM-1024x456.png 1024w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM-300x134.png 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM-768x342.png 768w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM-624x278.png 624w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2025\/01\/Screenshot-2025-01-03-at-8.18.46\u202fAM.png 1518w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>2024<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">41) Ash, J.; Kang, J. Y. &#8220;Synthesis of unsymmetrical phosphorus disulfides&#8221; <em>Org. Biomol. Chem.<\/em>, <strong>2024<\/strong>, <em>24<\/em>, 7492-7499. <a href=\"https:\/\/doi.org\/10.1039\/D4OB01099J\">https:\/\/doi.org\/10.1039\/D4OB01099J<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><a href=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2024\/09\/Get-2.gif\"><img loading=\"lazy\" decoding=\"async\" width=\"378\" height=\"177\" src=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2024\/09\/Get-2.gif\" alt=\"\" class=\"wp-image-816\"\/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">40) Ash, J.; Ahmed, M.; Le, N.; Huang, H.; Kang, J. Y. &#8220;Catalytic, regioselective Friedel\u2013Crafts alkylation of beta-naphthol&#8221; <em>New J. Chem.<\/em>, <strong>2024<\/strong>,<em>48<\/em>, 4224-4228. <a href=\"https:\/\/doi.org\/10.1039\/D3NJ05580A\">https:\/\/doi.org\/10.1039\/D3NJ05580A<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><a href=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2024\/03\/Get.gif\"><img loading=\"lazy\" decoding=\"async\" width=\"345\" height=\"189\" src=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2024\/03\/Get.gif\" alt=\"\" class=\"wp-image-810\"\/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>2023<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">(39) Ash, J.; Kang, J. Y. &#8220;Catalyst-free thiophosphorylation of&nbsp;<em>in situ<\/em>&nbsp;formed&nbsp;<em>ortho<\/em>-quinone methides&#8221; <em>Org. Biomol. Chem.<\/em>, <strong>2023<\/strong>, <em>21<\/em>, 2370-2374. DOI:<a href=\"https:\/\/doi.org\/10.1039\/D2OB02169B\">https:\/\/doi.org\/10.1039\/D2OB02169B<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><a href=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2023\/03\/OBC-2023.gif\"><img loading=\"lazy\" decoding=\"async\" width=\"378\" height=\"121\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2023\/03\/OBC-2023.gif\" alt=\"\" class=\"wp-image-799\" style=\"width:409px;height:131px\"\/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>2022<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">(38) Patent Issued<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Kang, J. Y.; Huang, H. \u201cChiral n-heterocyclic phosphorodiamidic acids (NHPAS) and derivatives as novel bronsted acid catalysts\u201d <a href=\"https:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;d=PALL&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&amp;r=1&amp;f=G&amp;l=50&amp;s1=11,248,014.PN.&amp;OS=PN\/11,248,014&amp;RS=PN\/11,248,014\"><strong><a href=\"https:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;d=PALL&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&amp;r=1&amp;f=G&amp;l=50&amp;s1=11,248,014.PN.&amp;OS=PN\/11,248,014&amp;RS=PN\/11,248,014\"><strong>11,248,014<\/strong><\/a><\/strong><\/a>, 2\/15\/2022<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">(37) Huang, H.;&nbsp; Kang, J. Y.&#8221;Triflic Anhydride (Tf2O)-Activated Transformation of Amides, Sulfoxides and Phosphorus Oxides via Nucleophilic Trapping&#8221;&nbsp;<em>Synthesis<\/em>,&nbsp;<strong>2022<\/strong>, <em>54<\/em>, 1157-1202. DOI:<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-1679-8205\">&nbsp;10.1055\/a-1679-8205<\/a> (Invited SYNTHESIS REVIEW article)<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><a href=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/11\/image.png\"><img loading=\"lazy\" decoding=\"async\" width=\"725\" height=\"357\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/11\/image.png\" alt=\"\" class=\"wp-image-778\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/11\/image.png 725w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/11\/image-300x148.png 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/11\/image-624x307.png 624w\" sizes=\"auto, (max-width: 725px) 100vw, 725px\" \/><\/a><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>2021<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">(36)&nbsp;Ash, J.; Huang, H.; Cordero, P.; J. Y. Kang &#8220;Selective hydrolysis of phosphorus(v) compounds to form organophosphorus monoacids&#8221; <em>Org. Biomol. Chem. <\/em><strong>2021<\/strong>,&nbsp;<em>19<\/em>, 6007-6014 <a href=\"https:\/\/doi.org\/10.1039\/D1OB00881A\">doi.org\/10.1039\/D1OB00881A<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><a href=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/06\/Get-2.gif\"><img loading=\"lazy\" decoding=\"async\" width=\"378\" height=\"90\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2021\/06\/Get-2.gif\" alt=\"\" class=\"wp-image-772\" style=\"width:453px;height:108px\"\/><\/a><\/figure>\n\n\n<p>(35) Patent Issued<\/p>\n<p>Kang, J. Y.; Huang, H. \u201cMetal-free direct arylation of dialkyl phosphonates for the synthesis of mixed alkyl aryl phosphonates\u201d <a href=\"http:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;d=PALL&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&amp;r=1&amp;f=G&amp;l=50&amp;s1=10927135.PN.&amp;OS=PN\/10927135&amp;RS=PN\/10927135\"><strong>10,927,135<\/strong><\/a>, 2\/23\/2021<\/p>\n<p><strong>2020<\/strong><\/p>\n<p>(34) Patent Issued<\/p>\n<p>Kang, J. Y.; Mulla, K.; Aleshire, K.; Forster, M P. &#8220;N-heterocyclic phosphines&#8221; <b><a href=\"http:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;d=PALL&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&amp;r=1&amp;f=G&amp;l=50&amp;s1=10,633,403.PN.&amp;OS=PN\/10,633,403&amp;RS=PN\/10,633,403\">10,633,403<\/a><\/b>, 4\/28\/2020<\/p>\n<p>(33)&nbsp;Le Pham, N. S.; Shin, H.; Kang, J. Y.; Sohn, J. H. &#8220;Oxidative Dehydrosulfurative Cross-Coupling of 3, 4-Dihydropyrimidine-2-thiones with Alkynes for Access to 2-Alkynylpyrimidines&#8221; <em>J. Org. Chem.&nbsp;<\/em><strong>2020<\/strong>,&nbsp;<em>85<\/em>, 5087-5096. <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.0c00091\">https:\/\/doi.org\/10.1021\/acs.joc.0c00091<\/a><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=765\" rel=\"attachment wp-att-765\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-765\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2020\/06\/jo0c00091_0007.gif\" alt=\"\" width=\"500\" height=\"138\"><\/a><\/p>\n<div>\n<p><strong>2019<\/strong><\/p>\n<p>(32) Patent Issued<\/p>\n<p>Kang, J. Y.; Huang, H.; Molleti, N. <span style=\"color: #000000;\">&#8220;<\/span><a class=\"gsc_a_at\" data-href=\"\/citations?view_op=view_citation&amp;hl=en&amp;user=vqcuRdcAAAAJ&amp;sortby=pubdate&amp;citation_for_view=vqcuRdcAAAAJ:4TOpqqG69KYC\"><span style=\"color: #000000;\">Functionalized phosphonates via Michael addition&#8221;,<\/span><\/a><a href=\"http:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;d=PALL&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&amp;r=1&amp;f=G&amp;l=50&amp;s1=10,435,423.PN.&amp;OS=PN\/10,435,423&amp;RS=PN\/10,435,423\">10,435,423<\/a>, 10\/8\/2019<\/p>\n<p>(31) <span class=\"ff5\"><span class=\"current-selection\"> Ash, J.; <\/span><\/span><span class=\"ff5\"><span class=\"current-selection\">Huang, H.; Kang, J. Y. &#8220;Metal- and Chloride Reagent-free Synthesis of Mixed Thiophosphates&#8221;&nbsp;<em>Org. Biomol. Chem.<\/em><strong>2019<\/strong>,&nbsp;<em>17<\/em>, 3812-3818. <a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2019\/OB\/C9OB00370C#!divAbstract\">DOI: 10.1039\/c9ob00370c<\/a><\/span><\/span><\/p>\n<div class=\"page\" title=\"Page 1\">\n<div class=\"section\">\n<div class=\"layoutArea\">\n<div class=\"column\"><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=727\" rel=\"attachment wp-att-727\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-727\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2019\/03\/Get-2.gif\" alt=\"\" width=\"378\" height=\"177\"><\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<p>(30)&nbsp;<span class=\"ff5\"><span class=\"current-selection\">Huang, H.;&nbsp; Kang, J. Y.&#8221;New Strategies for Activation of Phosphonates\/Phosphates to Forge Functional Phosphorus Compounds&#8221;&nbsp;<em>Synlett<\/em>,&nbsp;<strong>2019<\/strong>, <em>30<\/em>, 635-641. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0037-1611699\">10.1055\/s-0037-1611699<\/a><\/span><\/span>&nbsp;(Invited SYNPACTS article)<\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=710\" rel=\"attachment wp-att-710\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-710\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2019\/01\/Abstract-2.jpg\" alt=\"\" width=\"399\" height=\"183\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2019\/01\/Abstract-2.jpg 399w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2019\/01\/Abstract-2-300x138.jpg 300w\" sizes=\"auto, (max-width: 399px) 100vw, 399px\" \/><\/a><\/p>\n<p><span style=\"color: #ffffff;\"><a style=\"color: #ffffff;\" href=\"https:\/\/www.thieme.de\/en\/thieme-chemistry\/thieme-chemistry-journals-awardees-107362.htm\"><strong><span style=\"color: #ff0000;\"><span style=\"color: #000000;\">Jun Yong Kang:<\/span> Thieme Chemistry Journal Awardee in 2019<\/span><\/strong><\/a><\/span><\/p>\n<p><strong>2018<\/strong><\/p>\n<div class=\"t m0 x8 h9 ya ff4 fs6 fc2 sc0 ls1 ws0 citation-container\">\n<p>(29) Patent Issued<\/p>\n<p>Kang, J. Y.; Mulla, K. &#8220;Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues&#8221;, <a href=\"http:\/\/patft.uspto.gov\/netacgi\/nph-Parser?Sect1=PTO1&amp;Sect2=HITOFF&amp;p=1&amp;u=\/netahtml\/PTO\/srchnum.html&amp;r=1&amp;f=G&amp;l=50&amp;d=PALL&amp;s1=10087204.PN.\">US10087204B2<\/a>, 10\/2\/2018<\/p>\n<p>(28)&nbsp;<span class=\"ff5\"><span class=\"current-selection\">Huang, H.; Ash, J.; Kang, J. Y. &#8220;<\/span><\/span><span style=\"font-size: 1rem;\">Tf2O\u2010Promoted Activating Strategy of Phosphate Analogues:&nbsp;<\/span><span style=\"font-size: 1rem;\">Synthesis of Mixed Phosphates and Phosphinate&#8221;&nbsp;<span class=\"hlFld-Title\"><em>Org. Lett.&nbsp;<\/em><strong>2018<\/strong>,&nbsp;4938-4941<em>,&nbsp;<\/em>DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.8b02073\">10.1021\/acs.orglett.8b02073<\/a><\/span><\/span><\/p>\n<ul>\n<li><span style=\"color: #ff0000;\"><strong>Highlighted<\/strong><\/span>&nbsp;on the Organic Chemistry Portal. [<a style=\"font-size: 1rem;\" href=\"https:\/\/www.organic-chemistry.org\/abstracts\/lit6\/470.shtm\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a>]<\/li>\n<\/ul>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=692\" rel=\"attachment wp-att-692\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-692\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/08\/ol-2018-020735_0009.gif\" alt=\"\" width=\"419\" height=\"161\"><\/a><\/p>\n<p>(27)&nbsp;<span class=\"ff5\"><span class=\"current-selection\">Huang, H.; Ash, J.; Kang, J. Y. &#8220;Base-Controlled Fe(Pc)-Catalyzed Aerobic Oxidation of Thiols for the Synthesis of S-S and S-P(O) Bond&#8221;&nbsp;<i style=\"line-height: 1.714285714; font-size: 1rem;\">Org. Biomol. Chem.&nbsp;<\/i><strong style=\"line-height: 1.714285714; font-size: 1rem;\">2018<\/strong>, <em>16,&nbsp;<\/em>4236-4242,&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/C8OB00908B\">http:\/\/dx.doi.org\/10.1039\/C8OB00908B<\/a><\/span><\/span><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=683\" rel=\"attachment wp-att-683\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-683\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/TOC.jpg\" alt=\"\" width=\"437\" height=\"118\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/TOC.jpg 437w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/TOC-300x81.jpg 300w\" sizes=\"auto, (max-width: 437px) 100vw, 437px\" \/><\/a><\/p>\n<p><span class=\"ff5\"><span class=\"current-selection\">(26) Le, N.; Huang, H.; Kang, J. Y. &#8220;<\/span><\/span><span style=\"font-size: 1rem;\">One-pot synthesis of phosphorodiamidothioates using N-heterocyclic phosphine (NHP)-thiourea&#8221; <em>Tetrahedron Lett.&nbsp;<\/em><strong>2018<\/strong>, <em>56<\/em>, 2296-2298, <a href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2018.04.080\">https:\/\/doi.org\/10.1016\/j.tetlet.2018.04.080&nbsp;<\/a><\/span><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=678\" rel=\"attachment wp-att-678\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-678\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/1-s2.0-S0040403918305665-fx1.jpg\" alt=\"\" width=\"455\" height=\"142\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/1-s2.0-S0040403918305665-fx1.jpg 500w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/05\/1-s2.0-S0040403918305665-fx1-300x94.jpg 300w\" sizes=\"auto, (max-width: 455px) 100vw, 455px\" \/><\/a><\/p>\n<p><span class=\"ff5\"><span class=\"current-selection\">(25) Huang, H.; Zhu, H.; Kang, J. Y. &#8220;<\/span><\/span><span class=\"hlFld-Title\">Regio- and Stereoselective Hydrophosphorylation of Ynamides for the Synthesis of \u03b2-Aminovinylphosphine Oxides&#8221;&nbsp;<em>Org. Lett.&nbsp;<\/em><strong>2018<\/strong>, <i>20<\/i>, 2778-2781<em>,&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.8b01065\"><strong>DOI:&nbsp;<\/strong>10.1021\/acs.orglett.8b01065<\/a><\/em><\/span><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=675\" rel=\"attachment wp-att-675\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-675\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/04\/ol-2018-01065c_0008.gif\" alt=\"\" width=\"453\" height=\"162\"><\/a><\/p>\n<p><span class=\"ff5\"><span class=\"ff5\"><span class=\"current-selection\">(24) Huang, H.;<\/span><span class=\"enhanced-author d9bed797-7db1-4726-a78f-bbc17507a785 enhanced-underline-draw current-selection\">&nbsp;Denne<\/span><span class=\"current-selection\">, J.;&nbsp;<\/span><span class=\"enhanced-author 713753c4-dc3a-4e73-ac06-eafe1ee50cb0 enhanced-underline-draw current-selection\">Yang<\/span><span class=\"current-selection\">,&nbsp;<span class=\"enhanced-author 713753c4-dc3a-4e73-ac06-eafe1ee50cb0 enhanced-underline-draw current-selection\">C-H.;<\/span><\/span><span class=\"enhanced-author e8c5d918-5bc1-4b8b-847b-7945d65c34b4 enhanced-underline-draw current-selection\">&nbsp;Wang<\/span><span class=\"current-selection\">, H.; Kang, J. Y. &#8220;<\/span><\/span><\/span><span class=\"ff5\"><span class=\"current-selection\">Direct Aryloxylation\/Alkyloxylation of Dialkyl Phosphonat<\/span><span class=\"current-selection\">es for the&nbsp;<\/span><\/span><span style=\"font-size: 1rem;\">Synthesis of Mixed Phosphonates&#8221;&nbsp;<\/span><em><span class=\"current-selection\" style=\"font-size: 1rem;\">Angew<\/span><span class=\"current-selection\" style=\"font-size: 1rem;\">. Chem. Int. Ed.<\/span><\/em><span class=\"ff5 current-selection\" style=\"font-size: 1rem;\"><span class=\"hlFld-Title\"><strong>2018<\/strong>,&nbsp;<\/span><em>57<\/em>, 6624-6628,&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201802082\">http:\/\/dx.doi.org\/10.1002\/anie.201802082<\/a><\/span><\/p>\n<\/div>\n<\/div>\n<div><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=667\" rel=\"attachment wp-att-667\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-667\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/04\/ACIE.jpg\" alt=\"\" width=\"501\" height=\"140\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/04\/ACIE.jpg 429w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2018\/04\/ACIE-300x84.jpg 300w\" sizes=\"auto, (max-width: 501px) 100vw, 501px\" \/><\/a><\/div>\n<div>&nbsp;<\/div>\n<div>&nbsp;<\/div>\n<div>&nbsp;<\/div>\n<div>\n<p>(23) Shetty, M.; Huang, H.;&nbsp;Kang, J. Y.&nbsp;\u201c<span class=\"hlFld-Title\">Regioselective Synthesis of \u03b1- and <i>\u03b3-<\/i>Amino Quinolinyl Phosphonamides Using <i>N<\/i>-Heterocyclic Phosphines (NHPs)<\/span>&#8220;<em>Org. Lett.&nbsp;<\/em><strong>2018<\/strong>, <i>20<\/i>, 700-703, <a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.7b03829\">DOI: 10.1021\/acs.orglett.7b03829<\/a>.<\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=657\" rel=\"attachment wp-att-657\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-657\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-03829y_0010.gif\" alt=\"\" width=\"500\" height=\"127\"><\/a><\/p>\n<p><strong>2017<\/strong><\/p>\n<p>(22) Huang, H.;&nbsp;Kang, J. Y.&nbsp;\u201cOrganocatalytic Phosphonylation of In Situ Formed o-Quinone Methides&#8221;<em>Org. Lett.<\/em><strong>2017<\/strong>, <em>19<\/em>, 5988-5991, <span style=\"color: #00ccff;\"><a href=\"http:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.7b03019\">DOI: 10.1021\/acs.orglett.7b03019<\/a>.<\/span><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=647\" rel=\"attachment wp-att-647\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-647\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-030198_0008.jpeg\" alt=\"\" width=\"376\" height=\"169\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-030198_0008.jpeg 939w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-030198_0008-300x135.jpeg 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-030198_0008-768x345.jpeg 768w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2017-030198_0008-624x280.jpeg 624w\" sizes=\"auto, (max-width: 376px) 100vw, 376px\" \/><\/a><\/p>\n<p><span style=\"font-size: 1rem;\">Invention Disclosure<\/span><\/p>\n<p>(21) Jun Yong Kang, Hai Huang, \u201dMetal-free Direct Arylation of Dialkyl Phosphonates for the Synthesis of Mixed Alkyl Aryl Phosphonates\u201d, Filed with The Board of Regents of the Nevada System of Higher Education (NSHE) on Behalf of UNLV, 62540773, August 7,&nbsp;<strong>2017<\/strong><\/p>\n<p>(20) Jun Yong Kang, Hai Huang, \u201dChiral N-heterocyclic Phosphordiamidic Acids (NHPAS) and Derivatives as Novel Br\u00f8nsted Acid Catalysts\u201d,&nbsp;Filed with The Board of Regents of the Nevada System of Higher Education (NSHE) on Behalf of UNLV (62521086) &nbsp;June 16, <strong>2017<\/strong>.<\/p>\n<p>(19) Huang, H.; Kang, J. Y.,&nbsp;\u201cMitsunobu Reaction Using Basic Amines as Pronucleophiles&#8221; <em>J. Org. Chem.<\/em>, <strong style=\"font-size: 1rem;\">2017<\/strong>, <em>82<\/em>, 6604-6614<em style=\"font-size: 1rem;\">.<span style=\"color: #00ccff;\">&nbsp;<\/span><\/em><span style=\"color: #33cccc;\"><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b00622\">DOI:&nbsp;10.1021\/acs.joc.7b00622<\/a><\/span><\/p>\n<ul>\n<li><span style=\"color: #ff0000;\"><strong><a href=\"https:\/\/www.unlv.edu\/news-story\/chemist-partners-company-market-reagents\"><span style=\"color: #ff0000;\">NHP-Butane<\/span><\/a><\/strong> <strong>is available at <span style=\"color: #33cccc;\"><a href=\"https:\/\/www.kerafast.com\/product\/3347\/nhp-butane\"><span style=\"color: #008080;\">Kerafast<\/span><\/a><\/span><\/strong><\/span><\/li>\n<li><strong style=\"color: #ff0000; font-size: 1rem;\"><em><span style=\"color: #ff0000;\"><a href=\"http:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=month&amp;journalCode=joceah\"><span style=\"color: #ff0000;\">Most Read Articles in June July August 2017<\/span><\/a><\/span>&nbsp;<\/em><\/strong><\/li>\n<li><span style=\"color: #ff0000;\"><strong style=\"font-size: 1rem;\">Highlighted<\/strong><\/span> in <em style=\"font-size: 1rem;\">Synfacts<\/em>, <strong style=\"font-size: 1rem;\">2017<\/strong>, <em style=\"font-size: 1rem;\">13<\/em>, 807.&nbsp;<a style=\"font-size: 1rem;\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1590737\">DOI: 10.1055\/s-0036-1590737<\/a><\/li>\n<\/ul>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=606\" rel=\"attachment wp-att-606\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-606\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Picture1.png\" alt=\"Picture1\" width=\"388\" height=\"171\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Picture1.png 685w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Picture1-300x132.png 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Picture1-624x275.png 624w\" sizes=\"auto, (max-width: 388px) 100vw, 388px\" \/><\/a><\/p>\n<p>(18) Moletti, N.; Kang, J. Y.,&nbsp;\u201cSynthesis of Diaryl-Diazaphosphonates&nbsp;<i style=\"line-height: 1.714285714; font-size: 1rem;\">via&nbsp;<\/i>1,6-Hydrophosphonylation of<i style=\"line-height: 1.714285714; font-size: 1rem;\">&nbsp;p<\/i>-Quinone Methides with <em style=\"line-height: 1.714285714; font-size: 1rem;\">N<\/em>-Heterocyclic Phosphine-Thioureas\u201d&nbsp;<em style=\"line-height: 1.714285714; font-size: 1rem;\">Org. Lett.<\/em><strong style=\"line-height: 1.714285714; font-size: 1rem;\">2017<\/strong>, <em>19<\/em>, 958\u2013961&nbsp;DOI:<span style=\"color: #33cccc;\">&nbsp;<\/span><a style=\"line-height: 1.714285714; font-size: 1rem;\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.7b00261\"><span style=\"color: #33cccc;\"><span style=\"color: #00ccff;\"><span style=\"color: #33cccc;\"><span style=\"color: #008080;\">10.1021\/acs.orglett.7b00261<\/span><\/span><\/span><\/span><\/a><\/p>\n<ul>\n<li><strong><span style=\"color: #ff0000;\">NHP-Thiourea is available at<\/span> <a href=\"https:\/\/www.kerafast.com\/product\/3348\/nhp-thiourea\"><span style=\"color: #33cccc;\"><span style=\"color: #008080;\">Kerafast<\/span><\/span><\/a><\/strong><\/li>\n<\/ul>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=594\" rel=\"attachment wp-att-594\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-594\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-5-copy.jpg\" alt=\"Untitled OLMSW2000_2col_StyleSheet-5 copy\" width=\"361\" height=\"157\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-5-copy.jpg 601w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-5-copy-300x130.jpg 300w\" sizes=\"auto, (max-width: 361px) 100vw, 361px\" \/><\/a><\/p>\n<p>(17) Huang, H.; Kang, J. Y., &#8220;Oxidation-Reduction Condensation of Diazaphosphites for Carbon-Heteroatom Bond Formation Based on Mitsunobu Mechanism&#8221;&nbsp;<em style=\"line-height: 1.714285714; font-size: 1rem;\">Org. Lett.<\/em><strong style=\"line-height: 1.714285714; font-size: 1rem;\">2017<\/strong>,&nbsp;<em>19<\/em>, 544-547, DOI:&nbsp;<a style=\"line-height: 1.714285714; font-size: 1rem;\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.6b03709\">10.1021\/acs.orglett.6b03709<\/a><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=584\" rel=\"attachment wp-att-584\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-584\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-2.jpg\" alt=\"Untitled OLMSW2000_2col_StyleSheet-2\" width=\"322\" height=\"101\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-2.jpg 322w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Untitled-OLMSW2000_2col_StyleSheet-2-300x94.jpg 300w\" sizes=\"auto, (max-width: 322px) 100vw, 322px\" \/><\/a><\/p>\n<p><strong style=\"line-height: 1.714285714; font-size: 1rem;\">2016<\/strong><\/p>\n<p>(16) Huang, H.; Palmas, J.; Kang, J. Y., &#8220;A Reagent-Controlled Phospha-Michael Addition Reaction of Nitroalkenes with Bifunctional N-Heterocyclic Phosphine (NHP)-Thioureas&#8221;&nbsp;<em>J. Org. Chem.<\/em><strong>2016<\/strong>, <em>81,<\/em>&nbsp;11932\u201311939,&nbsp;DOI: <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.6b02490\">10.1021\/acs.joc.6b02490<\/a><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=557\" rel=\"attachment wp-att-557\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-557\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Table-of-contents.gif\" alt=\"Table of contents\" width=\"449\" height=\"123\"><\/a><\/p>\n<p>(15) Moletti, N.; Bjornberg, C.; Kang, J. Y. &#8220;Phospha-Michael addition reaction of maleimides employing N-heterocyclic phosphine-thiourea as a phosphonylation reagent: synthesis of 1-aryl-2,5-dioxopyrrolidine-3-yl-phosphonate derivatives&#8221;&nbsp;<i style=\"line-height: 1.714285714; font-size: 1rem;\">Org. Biomol. Chem.<\/i><strong style=\"line-height: 1.714285714; font-size: 1rem;\">2016<\/strong>, <em>14<\/em>, 10695-10704,&nbsp;DOI:&nbsp;<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/OB\/C6OB01987K#!divAbstract\">10.1039\/C6OB01987K<\/a><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=535\" rel=\"attachment wp-att-535\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-535\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/TOC.jpg\" alt=\"TOC\" width=\"294\" height=\"120\"><\/a><\/p>\n<p>(14) Moletti, N.;&nbsp;Kang, J. Y. &#8220;Catalyst-free synthesis of \u03b11-oxindole-\u03b1-hydroxyphosphonates via phospha-aldol reaction of isatins employing N-heterocyclic phosphine (NHP)-thiourea&#8221;&nbsp;<i style=\"font-size: 1rem; line-height: 1;\">Org. Biomol. Chem.<\/i><strong>2016<\/strong>, <em>14<\/em>, 8952-8956, DOI:&nbsp;<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/OB\/C6OB01608A#!divAbstract\">10.1039\/C6OB01608A<\/a><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=547\" rel=\"attachment wp-att-547\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-547\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/aldol.png\" alt=\"aldol\" width=\"363\" height=\"132\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/aldol.png 363w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/aldol-300x109.png 300w\" sizes=\"auto, (max-width: 363px) 100vw, 363px\" \/><\/a><\/p>\n<p>(13) Huang, H.; Kang, J. Y., &#8220;Amine-Catalyzed Phospha-Michael Reaction of&nbsp;\u03b1,\u03b2-Unsaturated Aldehydes and Ketones with Multifunctional <i style=\"line-height: 1.714285714; font-size: 1rem;\">N-<\/i>Heterocyclic Phosphine-Thioureas as Phosphonylation Reagent&#8221;&nbsp;<cite style=\"font-size: 1rem; line-height: 1;\">Org. Lett.<\/cite><strong style=\"font-size: 1rem; line-height: 1;\">2016<\/strong>, <em style=\"font-size: 1rem; line-height: 1;\">18<\/em>, 4372\u20134375,&nbsp;DOI:&nbsp;<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.6b02121\">10.1021\/acs.orglett.6b02121<\/a><\/p>\n<p><span style=\"font-size: 1rem;\">&nbsp;<\/span><\/p>\n<\/div>\n<div>\n<div><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=522\" rel=\"attachment wp-att-522\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-522\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/ol-2016-02121n_0012.gif\" alt=\"ol-2016-02121n_0012\" width=\"500\" height=\"153\"><\/a><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=534\" rel=\"attachment wp-att-534\"><br \/><\/a><\/div>\n<\/div>\n<div>&nbsp;<\/div>\n<p>(12) Mulla, K.; Kang, J. Y.,&nbsp;1,3,2-Diazaphospholidine (<i>N<\/i>-Heterocyclic Phosphine)-Mediated Carbon-Phosphorus Bond Forming One-Pot Tandem Reaction: A Route to \u03b1-amino Phosphonates, <em>J. Org. Chem.<\/em>&nbsp;<strong>2016<\/strong>,&nbsp;<em>81<\/em><strong>, <\/strong>4550-4558<em>,<strong>&nbsp;<\/strong><\/em>DOI:&nbsp;<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.6b00326\">10.1021\/acs.joc.6b00326<\/a><em><br \/><\/em><\/p>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=510\" rel=\"attachment wp-att-510\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-510\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/TOC-A-Route-to-\u03b1-amino-Phosphonates.png\" alt=\"TOC (A Route to \u03b1-amino Phosphonates)\" width=\"279\" height=\"110\"><\/a><\/p>\n<p>(11) Kang, J.-Y.; Johnston, R. C.; Snyder, K. M.; Cheong, P. H.-Y.; Carter, R. G.&nbsp;Construction of Stereogenic \u03b1,\u03b1-Disubstituted Cycloalkanones via 1\u00b0 Amine Thiourea Dual Catalysis: Experimental Scope and Computational Analyses&nbsp;<em style=\"line-height: 1.714285714; font-size: 1rem;\">J. Org. Chem.<\/em>&nbsp;<strong style=\"line-height: 1.714285714; font-size: 1rem;\">2016<\/strong>,&nbsp;<em style=\"line-height: 1.714285714; font-size: 1rem;\">81, <\/em>3629-3637<em style=\"line-height: 1.714285714; font-size: 1rem;\">&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;<\/em>DOI:&nbsp;<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.6b00280\">10.1021\/acs.joc.6b00280<\/a><\/p>\n<p><a style=\"line-height: 1.714285714; font-size: 1rem;\" href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=478\" rel=\"attachment wp-att-478\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-478\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/jo-2016-00280t_0014-TOC-300x241.gif\" alt=\"jo-2016-00280t_0014 TOC\" width=\"300\" height=\"241\"><\/a><\/p>\n<p>(10) Mulla, K.; Aleshire, K. L.;Forster, P. M.; Kang, J. Y.&nbsp;\u201cUtility of Bi-Functional <i>N<\/i>-Heterocyclic Phosphine (NHP)-Thioureas for Metal-Free Carbon-Phosphorus Bond Construction toward Regio-, and Stereoselective Formation of Vinylphosphonates\u201d,&nbsp;<em>J. Org. Chem.<\/em>&nbsp;<strong>2016<\/strong>, <em>81<\/em>, 77\u221288,&nbsp;DOI:<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.5b02184\">10.1021\/acs.joc.5b02184<\/a><\/p>\n<ul>\n<li><strong><span style=\"color: #ff0000;\">NHP-Thiourea is available at <\/span><a href=\"https:\/\/www.kerafast.com\/product\/3348\/nhp-thiourea\"><span style=\"color: #ff0000;\"><span style=\"color: #00ffff;\"><span style=\"color: #33cccc;\"><span style=\"color: #008080;\">Kerafast<\/span><\/span><\/span><\/span><\/a><\/strong><\/li>\n<\/ul>\n<p><a style=\"line-height: 1.714285714; font-size: 1rem;\" href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=470\" rel=\"attachment wp-att-470\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-470\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/NHP-thiourea--300x140.png\" alt=\"NHP thiourea\" width=\"300\" height=\"140\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/NHP-thiourea--300x140.png 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/NHP-thiourea--1024x479.png 1024w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/NHP-thiourea--624x291.png 624w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p>(9) El-Mansy, M. F.,&nbsp;Kang, J.-Y.; Lingampally, R.,&nbsp;Carter, R. G.,&nbsp;Proline Sulfonamide-Catalyzed, Domino Process for Asymmetric&nbsp;Synthesis of Amino- and Hydroxy-Substituted&nbsp;Bicyclo[2.2.2]octanes.&nbsp;<em>Eur. J. Org. Chem<\/em>.&nbsp;<strong>2016<\/strong>, 150\u2013157,&nbsp;DOI:<a href=\"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1002\/ejoc.201501302\/full\">10.1002\/ejoc.201501302<\/a><a style=\"line-height: 1.714285714; font-size: 1rem;\" href=\"http:\/\/jkang.faculty.unlv.edu\/?attachment_id=462\" rel=\"attachment wp-att-462\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-462\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/222-bicyclo-300x75.jpg\" alt=\"[2,2,2]-bicyclo\" width=\"300\" height=\"75\" srcset=\"https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/222-bicyclo-300x75.jpg 300w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/222-bicyclo-624x157.jpg 624w, https:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/222-bicyclo.jpg 675w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p>Invention Disclosure<\/p>\n<p>(8) Jun Yong Kang, Hai Huang, Nagaraju Molleti,&nbsp;Functionalized Phosphonates via Michael Addition,&nbsp;Filed with The Board of Regents of the Nevada System of Higher Education (NSHE) on Behalf of UNLV (62376213)&nbsp;August 17,&nbsp;<strong style=\"line-height: 1.714285714; font-size: 1rem;\">2016<\/strong>.<\/p>\n<p><strong>2015<\/strong><\/p>\n<p>Invention Disclosure<\/p>\n<p>(7) Jun Yong Kang, Karimulla Mulla,&nbsp;Methods and Compositions for Substituted Alpha-Aminophosphonates Analogues,&nbsp;Filed with The Board of Regents of the Nevada System of Higher Education (NSHE) on Behalf of UNLV (62309674)&nbsp;March 17,&nbsp;<strong>2015<\/strong>.<\/p>\n<p><strong>2014<\/strong><\/p>\n<p>Invention Disclosure<\/p>\n<p>(6) Jun Yong Kang, Karimulla Mulla, Kyle Aleshire, Paul M Forster,&nbsp;N-Heterocyclic Phosphines,&nbsp;Filed with The Board of Regents of the Nevada System of Higher Education (NSHE) on Behalf of UNLV (62048072) September 9, <strong>2014<\/strong>.<\/p>\n<p><strong>Before UNLV<\/strong><\/p>\n<p>(5) Kang, J.-Y.; Carter, R. G., <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol301272r\">Primary Amine, Thiourea-Based Dual Catalysis Motif for Synthesis of Stereogenic, All-Carbon Quaternary Center-Containing Cycloalkanones<\/a>. <em>Org. Lett.<\/em>&nbsp;<strong>2012<\/strong>, <em>14<\/em>, 3178-3181.<br \/><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-314\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Org.-Lett.-2012-14-12-pp-3178\u20133181-300x152.gif\" alt=\"Org. Lett., 2012, 14 (12), pp 3178\u20133181\" width=\"300\" height=\"152\"><br \/>(4) Kang, J.-Y.; Connell, B. T., <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo200939u\">Palladium-Catalyzed Alkynylation of Secondary \u03b1-Bromo Carbonyl Compounds by the Still Coupling Reaction between sp and sp3 Carbons<\/a>. <em>J. Org. Chem.<\/em>&nbsp;<strong>2011<\/strong>, <em>76<\/em>, 6856-6859.<br \/><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-313\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/J.-Org.-Chem.-2011-76-16-pp-6856\u20136859-300x100.gif\" alt=\"J. Org. Chem., 2011, 76 (16), pp 6856\u20136859\" width=\"300\" height=\"100\"><br \/>(3) Kang, J.-Y.; Connell, B. T., <a href=\"http:\/\/Efficient Synthesis of Substituted Acetylenic \u03b1,\u03b2-Epoxides Followed by Indium-Catalyzed Rearrangement to 2,3,5-Trisubstituted Furans\" data-wplink-url-error=\"true\">Synthesis of Substituted Acetylenic \u03b1,\u03b2-Epoxides Followed by Indium-Catalyzed Rearrangement to 2,3,5-Trisubstituted Furans<\/a>. <em>J. Org. Chem.<\/em>&nbsp;<strong>2011<\/strong>, <em>76<\/em>, 2379-2383.<\/p>\n<ul>\n<li><span style=\"font-size: 1rem;\"><strong><span style=\"color: #ff0000;\">Highlighted<\/span><\/strong>&nbsp;in&nbsp;<em>Synfacts<\/em>,&nbsp;<strong>2011<\/strong>,&nbsp;<em>8<\/em>, 607. [<\/span><a style=\"font-size: 1rem;\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0030-1260455\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a><span style=\"font-size: 1rem;\">]<\/span><\/li>\n<li><span style=\"font-size: 1rem;\"><span style=\"color: #ff0000;\"><strong>Highlighted<\/strong><\/span>&nbsp;on the Organic Chemistry Portal. [<\/span><a style=\"font-size: 1rem;\" href=\"http:\/\/www.organic-chemistry.org\/abstracts\/lit3\/236.shtm\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a><span style=\"font-size: 1rem;\">]<\/span><\/li>\n<\/ul>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-312\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/J.-Org.-Chem.-2011-76-7-pp-2379\u20132383-300x67.gif\" alt=\"J. Org. Chem., 2011, 76 (7), pp 2379\u20132383\" width=\"300\" height=\"67\"><br \/>(2) Kang, J.-Y.; Connell, B. T., <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/ja910057g\">Chromium-Catalyzed Homoaldol Equivalent Reaction Employing a Nucleophilic Propenyl Acetate.<\/a>&nbsp;&nbsp;<em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2010<\/strong>, <em>132<\/em>, 7826-7827.<\/p>\n<ul>\n<li><span style=\"font-size: 1rem;\">&nbsp;<\/span><span style=\"color: #ff0000;\"><strong style=\"font-size: 1rem;\">Highlighted<\/strong><\/span><span style=\"font-size: 1rem;\">&nbsp;in&nbsp;<\/span><em style=\"font-size: 1rem;\">Synfacts<\/em><span style=\"font-size: 1rem;\">,&nbsp;<\/span><strong style=\"font-size: 1rem;\">2010<\/strong><span style=\"font-size: 1rem;\">,&nbsp;<\/span><em style=\"font-size: 1rem;\">7<\/em><span style=\"font-size: 1rem;\">, 1063. [<\/span><a style=\"font-size: 1rem;\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0030-1257895\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a><span style=\"font-size: 1rem;\">]<\/span><\/li>\n<li>&nbsp;<span style=\"color: #ff0000;\"><strong>Highlighted<\/strong><\/span>&nbsp;on the Organic Chemistry Portal. [<a style=\"font-size: 1rem;\" href=\"http:\/\/www.organic-chemistry.org\/abstracts\/lit2\/926.shtm\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a>]<\/li>\n<li>&nbsp;<span style=\"color: #ff0000;\"><strong>Highlighted<\/strong><\/span>&nbsp;in&nbsp;New Methods for C-C Bond Construction, February 2011. [<a style=\"font-size: 1rem;\" href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2011\/21February.shtm\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a>]<\/li>\n<\/ul>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-311\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/J.-Am.-Chem.-Soc.-2010-132-23-pp-7826\u20137827-300x95.gif\" alt=\"J. Am. Chem. Soc., 2010, 132 (23), pp 7826\u20137827\" width=\"300\" height=\"95\"><br \/>(1) Kang, J.-Y.; Bugarin, A.; Connell, B. T., <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2008\/cc\/b806374e#!divAbstract\">Conversion of Nitrosobenzenes to Isoxazolidines: An Efficient Cascade Process Utilizing Reactive Nitrone Intermediates<\/a>.&nbsp;<em>Chem. Commun.<\/em>&nbsp;<strong>2008<\/strong>, 3522-3524.<\/p>\n<ul>\n<li><span style=\"font-size: 1rem;\"><strong><span style=\"color: #ff0000;\">Highlighted<\/span><\/strong>&nbsp;as a&nbsp;<strong><span style=\"color: #ff0000;\">Hot<\/span><\/strong>&nbsp;Article. [<\/span><a style=\"font-size: 1rem;\" href=\"http:\/\/www.rsc.org\/Publishing\/Journals\/cc\/News\/B806374E_Conell_080708.asp\" target=\"_blank\" rel=\"noopener noreferrer\">link<\/a><span style=\"font-size: 1rem;\">]<\/span><\/li>\n<\/ul>\n<p><a href=\"http:\/\/jkang.faculty.unlv.edu\/publication\/chem-comm-2008\/\" rel=\"attachment wp-att-310\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-310\" src=\"http:\/\/jkang.faculty.unlv.edu\/wp-content\/uploads\/2014\/06\/Chem-Comm-2008-300x100.gif\" alt=\"Chem Comm, 2008\" width=\"300\" height=\"100\"><\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>2026 44) Bhowmik, S.; Odoh, S. O.; Kang, J. Y. &#8220;Hydropersulfide-Mediated Stereoselective and Regioselective Hydrothiolation of P-alkynes&#8221; Organic Letters 2026, 28, 9371-9376. DOI: 10.1021\/acs.orglett.6c02541. 43) Bhowmik, S.; Kang, J. Y. &#8220;A concise synthesis of alkyl, aryl hydropersulfides&#8221; RSC Advances 2026, 16, 37522-37526. DOI: 10.1039\/d6ra03773a\u00a0 2025 42) Ash, J.; Curtis, K.; Bhowmik, S.; Odoh, S. O.; [&hellip;]<\/p>\n","protected":false},"author":238,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-110","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/pages\/110","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/users\/238"}],"replies":[{"embeddable":true,"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=110"}],"version-history":[{"count":160,"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/pages\/110\/revisions"}],"predecessor-version":[{"id":848,"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=\/wp\/v2\/pages\/110\/revisions\/848"}],"wp:attachment":[{"href":"https:\/\/jkang.faculty.unlv.edu\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=110"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}