{"id":7,"date":"2018-11-16T16:13:42","date_gmt":"2018-11-16T21:13:42","guid":{"rendered":"http:\/\/orgmedchem.nipissingu.ca\/?page_id=7"},"modified":"2026-07-15T09:40:20","modified_gmt":"2026-07-15T13:40:20","slug":"publications","status":"publish","type":"page","link":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<p class=\"vv_hanging_indent\"><em>Student Trainees are underlined<\/em><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* Amitabh Jha. From Spice to Scaffold: Design and Development of Curcumin Analogs to Combat Pancreatic Cancer. <em>Organics<\/em>, <strong>2026<\/strong>, <em>7<\/em>, 30. <a href=\"https:\/\/www.mdpi.com\/2673-401X\/7\/3\/30\" target=\"_blank\" rel=\"noopener noreferrer\" data-wp-editing=\"1\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* Dani Youssef, Haley Sheehy, Amitabh Jha. Synthesis and pharmacology of clinical drugs containing isoindoline heterocycle core. <em>Organics<\/em>, <strong>2025<\/strong>, <em>6<\/em>, 3. <a href=\"https:\/\/www.mdpi.com\/2673-401X\/6\/1\/3\" target=\"_blank\" rel=\"noopener noreferrer\" data-wp-editing=\"1\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<div id=\"attachment_275\" style=\"width: 219px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-275\" class=\"wp-image-275 size-medium\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-209x300.png\" alt=\"\" width=\"209\" height=\"300\" srcset=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-209x300.png 209w, https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-713x1024.png 713w, https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-768x1102.png 768w, https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-1070x1536.png 1070w, https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3-1427x2048.png 1427w, https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/03\/Organics-Journal-Issue-V6-I1-hd-3.png 2008w\" sizes=\"auto, (max-width: 209px) 100vw, 209px\" \/><\/p>\n<p id=\"caption-attachment-275\" class=\"wp-caption-text\">Our article has been highlighted as the cover story<\/p>\n<\/div>\n<p style=\"text-align: center\"><a href=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2025\/12\/Organics-Editors-Choice-Article-Certificate-print_19.pdf\" target=\"_blank\" rel=\"noopener\">Organics-Editor\u2019s Choice Article Certificate<\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Ryoga Hojo<\/span>, <span style=\"text-decoration: underline\">Spencer Short<\/span>, Mukund Jha.* Synthesis of 1,2-fused tricyclic indoles via Cu-\/base-mediated hydroamination of alkynes. <em>The<\/em>\u00a0<em>Journal of Organic Chemistry<\/em>, <strong>2019<\/strong>, 84, 16095-16104. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.joc.9b02591\" target=\"_blank\" rel=\"noopener noreferrer\" data-wp-editing=\"1\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Spencer Short<\/span>, <span style=\"text-decoration: underline\">Steven Rhodes<\/span>, Vishakha S. Bhave, <span style=\"text-decoration: underline\">Ryoga Hojo<\/span>, Mukund Jha.* Metal-free hydroamination of alkynes: A mild and concise synthesis of thiazole[3,2-<em>a<\/em>]indoles. <em>Synthesis<\/em>, <strong>2019<\/strong>, 51, 4263-4270. <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0039-1690680\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Steven Rhodes<\/span>, <span style=\"text-decoration: underline\">Spencer Short<\/span>, Sidhika Sharma, Ramneet Kaur, Mukund Jha.* One-pot mild and efficient synthesis of [1,3]thiazino[3,2-<em>a<\/em>]indol-4-ones and their anti-proliferative activity. <em>Organic &amp; Biomolecular Chemistry<\/em>, <strong>2019<\/strong>, 17, 3914-3920. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/ob\/c9ob00500e#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Shiv Dhiman<\/span>, Nitesh K. Nandwana, Hitesh K. Saini, Dalip Kumar, Krishnan Rangan, Katherine Robertson, Mukund Jha, Anil Kumar. Nickel-catalyzed tandem Knoevenagel condensation and intramolecular direct arylation: Synthesis of pyrazolo[5,1-a]isoquinoline derivatives. <em>Advanced Synthesis &amp; Catalysis<\/em>, <strong>2018<\/strong>, 360, 1973-1983. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.201701519\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Shiv Dhiman<\/span>, <span style=\"text-decoration: underline\">Steven Rhodes<\/span>, Dalip Kumar, Anil Kumar, Mukund Jha.* Copper-catalyzed tandem imine formation, Shonogashira coupling and intramolecular hydroamination: A facile synthesis of 3-aryl-\u03b3-carbolines. <em>ChemistrySelect<\/em>, <strong>2017<\/strong>, 2, 8922-8926.\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/slct.201702025\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Shiv Dhiman<\/span>, T. Stanley Cameron, Dalip Kumar, Anil Kumar. Au-Catalyzed synthesis of thiopyrano[2,3-b]indoles featuring tandem rearrangement and hydroarylation. <em>Organic Letters<\/em>, <strong>2017<\/strong>, 19, 2038-204.\u00a0<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.7b00617\" target=\"_blank\" rel=\"noopener noreferrer\" data-wp-editing=\"1\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mahesh Akula, P. Yogeeswari, D. Sriram, Mukund Jha, Anupam Bhattacharya. Synthesis and anti-tubercular activity of fused thieno-\/furo-quinoline compounds. <em>RSC Advances<\/em>, <strong>2016<\/strong>, 6, 46073-46080.\u00a0<a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/RA\/c6ra03187k#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, Mukund Jha,* Anil Kumar. Synthesis of indole-annulated sulfur heterocycles using copper catalyzed C-N coupling and palladium-catalyzed direct arylation. <em>Organic &amp; Biomolecular Chemistry<\/em>, <strong>2016<\/strong>, 14, 3450-3458.\u00a0<a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/OB\/C6OB00117C#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\" data-wp-editing=\"1\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Yadagiri Thigulla, Mahesh Akula, Prakruti Trivedi, Balram Ghosh, Mukund Jha, Anupam Bhattacharya. Synthesis and anti-cancer activity of 1,4-disubstituted imidazo[4,5-c]quinolines. <em>Organic &amp; Biomolecular Chemistry<\/em>, <strong>2016<\/strong>, 14, 876-883.\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/ob\/c5ob01650a#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">V. Kameshmysore Rao, <span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, <span style=\"text-decoration: underline\">Ashley Ryan<\/span>, Mukund Jha, Anil Kumar. Iodine-mediated microwave assisted synthesis of 2-arylnaphthofurans via cyclization of 1-(1\u2019-arylvinyl)-2-naphthols. <em>Synthesis<\/em>, <strong>2015<\/strong>, 47, 3990-3996.\u00a0<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1560268\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, T. Stanley Cameron, Anil Kumar. Access to substituted dihydrothiopyrano[2,3-b]indoles via sequential rearrangements during S-alkylation and Au-catalyzed hydroarylation on indoline-2-thiones. <em>The\u00a0Journal of Organic Chemistry<\/em>, <strong>2015<\/strong>, 80, 5272-5270.\u00a0<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jo5025943\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mahesh Akula, Yadagiri Thigulla, <span style=\"text-decoration: underline\">Connor Davis<\/span>, Mukund Jha, Anupam Bhattacharya. Synthesis of 4-substituted oxazole[4,5-c]quinolines by direct reaction at C-4 position of oxazoles. <em>Organic &amp; Biomolecular Chemistry<\/em>, <strong>2015<\/strong>, 13, 2600-2605.\u00a0<a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2015\/OB\/c4ob02224f#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, V. Kameshmysore Rao, Mukund Jha, T. Stanley Cameron, Anil Kumar. Microwave assisted catalyst-free synthesis of substituted 1,2,4-triazoles. <em>Synlett<\/em>, <strong>2015<\/strong>, 26, 404-407.\u00a0<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0034-1379734\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Connor Davis<\/span>, <span style=\"text-decoration: underline\">Julia Fazzari<\/span>, <span style=\"text-decoration: underline\">Mario Vitali<\/span>. BF3 Etherate-mediated microwave-assisted synthesis of thiopyrano[2,3-b]-2-ones. <em>Tetrahedron Letters<\/em>, <strong>2014<\/strong>, 55, 7043-7046.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403914018383\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Michael Edmunds<\/span>, <span style=\"text-decoration: underline\">Kate-Lyn Lund<\/span>, <span style=\"text-decoration: underline\">Ashley Ryan<\/span>. A new route to the versatile synthesis of 5H-thiopyrano[2,3-b:6,5-b\u2019]diindoles via 2-(alkylthio)-indole-3-carbaldehydes. <em>Tetrahedron Letters<\/em>, <strong>2014<\/strong>, 55, 5691-5694.\u00a0<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403914014531\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, Kasiviswanadharaju Pericherla, Anil Kumar. Microwave assisted copper triflate-catalyzed rapid hydration of aryl acetylenes. <em>Tetrahedron Letters<\/em>, <strong>2014<\/strong>, 55, 4814-4816.\u00a0<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S004040391401140X\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha,* <span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, Anil Kumar. Catalyst-free one-pot tandem reduction of oxo- and ene-\/yne- functionalities by hydrazine: Synthesis of substituted oxindoles from isatins. <em>European Journal of Organic Chemistry<\/em>, <strong>2014<\/strong>, 3334-3336.\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ejoc.201402038\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Manoj K. Muthyala, S Choudhary, Khima Pandey, <span style=\"text-decoration: underline\">Ganesh M. Shelke<\/span>, Mukund Jha, Anil Kumar. Synthesis of ionic liquid-supported diaryliodonium salts. <em>European Journal of Organic Chemistry<\/em>, <strong>2014<\/strong>, 2365-2370.\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ejoc.201301920\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\"><span style=\"text-decoration: underline\">Darian Blanchard<\/span>, T. Stanley Cameron, Mukund Jha*. Bronstead acid-catalyzed rapid enol-ether formation of 2-hydroxyindole-3-carboxaldehydes. <em>Molecular Diversity<\/em>, <strong>2013<\/strong>, 17, 827-834.\u00a0<a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs11030-013-9470-x\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha*, <span style=\"text-decoration: underline\">Stephanie Guy<\/span>, <span style=\"text-decoration: underline\">Ting-Yi Chou<\/span>. Microwave assisted synthesis of indole-annulated dihydropyrano[3,4-c]chromene derivatives via hetero-Diels-Alder reaction. <em>Tetrahedron Letters<\/em>, <strong>2011<\/strong>, 52, 4337-4341.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403911009920\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha*, <span style=\"text-decoration: underline\">Oro Enaohwo<\/span>, <span style=\"text-decoration: underline\">Stephanie Guy<\/span>. Yttrium triflate-catalyzed efficient chemoselective S-benzylation of indoline-2-thiones using benzyl alcohols. <em>Tetrahedron Letters<\/em>, <strong>2011<\/strong>,\u00a052, 684-687.\u00a0<a href=\"http:\/\/ac.els-cdn.com\/S0040403910022082\/1-s2.0-S0040403910022082-main.pdf?_tid=62b0813c-60ee-11e3-88e1-00000aab0f02&amp;acdnat=1386606452_81331d1268048dd0ca9d8eed956b6488\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha*, <span style=\"text-decoration: underline\">Ting-Yi Chou<\/span>, <span style=\"text-decoration: underline\">Brian Blunt<\/span>. General synthesis of mono-, di-, and tri-acetylated indoles from indolin-2-ones. <em>Tetrahedron<\/em>, <strong>2011<\/strong>, 67, 982-989.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402010017941\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha*, <span style=\"text-decoration: underline\">Oro Enaohwo<\/span>, Ashley Marcellus. Chemoselective S-benzylation of indoline-2-thiones using benzyl alcohols. <em>Tetrahedron Letters<\/em>, <strong>2009<\/strong>, 50, 7184-7187.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403909019959\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha*, <span style=\"text-decoration: underline\">Brian Blunt<\/span>. Highly efficient one-pot C-, N-, O- acylation of indolin-2-one analogs. <em>Tetrahedron Letters<\/em>, <strong>2009<\/strong>, 50, 6044-6047.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403909016165\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-42 size-full\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Susheel J. Nara, Mukund Jha, Johan Brinkhorst, Tony J. Zemneck, Derek A. Pratt. A simple Cu-catalyzed coupling approach to substituted 3-pyridinols and 5-pyrimidinols. <em>Journal of Organic Chemistry<\/em>, <strong>2008<\/strong>, 73, 9326-9333.\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/jo801501e\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Zoran Minic, Mukund Jha. Purification, functional characterization and inhibition of Brassinin Oxidase, a fungal detoxifying enzyme to overcome plant defenses. <em>FEBS Journal<\/em>, <strong>2008<\/strong>, 275, 3691-3705.\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1742-4658.2008.06513.x\/pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha, Derek A. Pratt. Kinetic solvent effects on peroxyl radical reactions. <em>Chemical Communications<\/em>, <strong>2008<\/strong>, 1252-1254.\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticlePDF\/2008\/CC\/B800369F\/2008-02-08?page=Search\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Mukund Jha, Zoran Minic, Oladapo G. Okeola. Isosteric probes provide structural requirements for detoxification of the phytoalexin brassinin by the fungal pathogen Leptosphaeria maculans. <em>Bioorganic and Medicinal Chemistry<\/em>, <strong>2007<\/strong>, 15, 6054-6061.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science?_ob=MImg&amp;_imagekey=B6TF8-4P29K7V-2-1N&amp;_cdi=5220&amp;_user=1069247&amp;_pii=S0968089607005780&amp;_origin=search&amp;_coverDate=09%2F15%2F2007&amp;_sk=999849981&amp;view=c&amp;wchp=dGLzVtb-zSkzS&amp;md5=3f6f41b18d14c3a4ca10ffad427e4d3b&amp;ie=\/sdarticle.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Ravi S. Gadagi, Mukund Jha, Vijay K. S. Mamillapalle. Detoxification of the phytoalexin brassinin by isolates of Leptosphaeria maculans involves an inducible hydrolase. <em>Phytochemistry<\/em>, <strong>2007<\/strong>, 68, 1572-1578.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science?_ob=MImg&amp;_imagekey=B6TH7-4NM5SC0-1-N&amp;_cdi=5275&amp;_user=1069247&amp;_pii=S003194220700177X&amp;_origin=search&amp;_coverDate=06%2F30%2F2007&amp;_sk=999319988&amp;view=c&amp;wchp=dGLbVlb-zSkzk&amp;md5=a3a8fda278a592af99e7203763536b4f&amp;ie=\/sdarticle.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Adewale M. Adio, Mojmir Suchy, Denis P. O. Okinyo, Qing-An Zheng, Mukund Jha, Mohammed G. Sarwar. Detection, characterization and identification of crucifer phytoalexins using high-performance liquid chromatography diode array and electrospray ionization tandem mass spectrometry analyses. <em>Journal of Chromatography A<\/em>, <strong>2006<\/strong>, 1133, 171-183.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science?_ob=MImg&amp;_imagekey=B6TG8-4KSVG2X-4-1&amp;_cdi=5248&amp;_user=1069247&amp;_pii=S0021967306015366&amp;_origin=search&amp;_coverDate=11%2F10%2F2006&amp;_sk=988669998&amp;view=c&amp;wchp=dGLbVtb-zSkWA&amp;md5=6149779d136b7084682fc0082fe31501&amp;ie=\/sdarticle.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Oladapo G. Okeola; Mukund Jha; M. Soledade C. Pedras*. Isolation of brassinin oxidase from phytopathogenic fungus Leptosphaeria maculans. <em>Canadian Journal of Plant Pathology<\/em>, <strong>2006<\/strong>, 28, 334.\u00a0<a href=\"http:\/\/www.tandfonline.com\/doi\/pdf\/10.1080\/07060660609507305\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Mukund Jha. Towards the control of Leptosphaeria maculans: design, synthesis, biological activity and metabolism of potential inhibitors of detoxification of the crucifer phytoalexin brassinin. <em>Bioorganic and Medicinal Chemistry<\/em>, <strong>2006<\/strong>, 14, 4958-4979.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science?_ob=MImg&amp;_imagekey=B6TF8-4JRKCV5-1-X&amp;_cdi=5220&amp;_user=1069247&amp;_pii=S0968089606002100&amp;_origin=search&amp;_coverDate=07%2F15%2F2006&amp;_sk=999859985&amp;view=c&amp;wchp=dGLzVzz-zSkWA&amp;md5=731f5d81844b7a170eb7afc46385d91a&amp;ie=\/sdarticle.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Mukund Jha, Oladapo G. Okeola. Camalexin induces detoxification of the phytoalexin brassinin in the plant pathogen Leptosphaeria maculans. <em>Phytochemistry<\/em>, <strong>2005<\/strong>, 66, 2609-2616.\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science?_ob=MImg&amp;_imagekey=B6TH7-4HG6FX5-1-R&amp;_cdi=5275&amp;_user=1069247&amp;_pii=S0031942205004632&amp;_origin=search&amp;_coverDate=11%2F30%2F2005&amp;_sk=999339977&amp;view=c&amp;wchp=dGLzVtz-zSkzk&amp;md5=cedb2f287f1f58587880918968dca801&amp;ie=\/sdarticle.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">Mukund Jha, M. Soledade C. Pedras, Effect of camalexin and spirobrassinin on the rate of detoxification of the phytoalexin brassinin by L. maculans. <em>Canadian Journal of Plant Pathology,<\/em> <strong>2005<\/strong>, 27, 167.\u00a0<a href=\"http:\/\/www.tandfonline.com\/doi\/pdf\/10.1080\/07060660509507211\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Mukund Jha. Concise syntheses of the cruciferous phytoalexins brassilexin, sinalexin, wasalexins and analogs: Expanding the scope of the Vilsmeier formylation. <em>Journal of Organic Chemistry<\/em>, <strong>2005<\/strong>, 70, 1828-1834.\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/jo0479866\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-42\" style=\"border: 0px\" src=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-content\/uploads\/sites\/81\/2018\/11\/pdf_symbol.gif\" alt=\"PDF\" width=\"19\" height=\"17\" \/><\/a><\/p>\n<p class=\"vv_hanging_indent\">M. Soledade C. Pedras, Mukund Jha, Pearson W. K. Ahiahonu. The synthesis and biosynthesis of phytoalexins produced by cruciferous plants. <em>Current Organic Chemistry<\/em>, <strong>2003<\/strong>, 7, 1635-1647.<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Student Trainees are underlined Mukund Jha,* Amitabh Jha. From Spice to Scaffold: Design and Development of Curcumin Analogs to Combat Pancreatic Cancer. Organics, 2026, 7, 30. Mukund Jha,* Dani Youssef, Haley Sheehy, Amitabh Jha. Synthesis and pharmacology of clinical drugs containing isoindoline heterocycle core. Organics, 2025, 6, 3. Organics-Editor\u2019s Choice Article Certificate Ryoga Hojo, Spencer <a class=\"more-link\" href=\"https:\/\/wpms.nipissingu.ca\/orgmedchem\/publications\/\">Read More &#8230;<\/a><\/p>\n","protected":false},"author":654,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-7","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/pages\/7","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/users\/654"}],"replies":[{"embeddable":true,"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/comments?post=7"}],"version-history":[{"count":39,"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/pages\/7\/revisions"}],"predecessor-version":[{"id":299,"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/pages\/7\/revisions\/299"}],"wp:attachment":[{"href":"https:\/\/wpms.nipissingu.ca\/orgmedchem\/wp-json\/wp\/v2\/media?parent=7"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}