PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones
© The Royal Society of Chemistry 2015. A highly efficient metal-free decarboxylative sulfonylation protocol for the preparation of (E)-vinyl sulfones from of β-aryl-α,β-unsaturated carboxylic acids using sodium sulfinates and (diacetoxyiodo)benzene (PhI(OAc)<inf>2</inf>) was developed. T...
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th-mahidol.354642018-11-23T16:57:07Z PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones Praewpan Katrun Sornsiri Hlekhlai Jatuporn Meesin Manat Pohmakotr Vichai Reutrakul Thaworn Jaipetch Darunee Soorukram Chutima Kuhakarn Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry © The Royal Society of Chemistry 2015. A highly efficient metal-free decarboxylative sulfonylation protocol for the preparation of (E)-vinyl sulfones from of β-aryl-α,β-unsaturated carboxylic acids using sodium sulfinates and (diacetoxyiodo)benzene (PhI(OAc)<inf>2</inf>) was developed. This strategy offers a simple and expedient synthesis of (E)-vinyl sulfones bearing a wide variety of functional groups. A radical-based pathway has been proposed for this decarboxylative sulfonylation reaction. 2018-11-23T09:43:46Z 2018-11-23T09:43:46Z 2015-04-28 Article Organic and Biomolecular Chemistry. Vol.13, No.16 (2015), 4785-4794 10.1039/c5ob00417a 14770520 2-s2.0-84927615292 https://repository.li.mahidol.ac.th/handle/123456789/35464 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84927615292&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Praewpan Katrun Sornsiri Hlekhlai Jatuporn Meesin Manat Pohmakotr Vichai Reutrakul Thaworn Jaipetch Darunee Soorukram Chutima Kuhakarn PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
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© The Royal Society of Chemistry 2015. A highly efficient metal-free decarboxylative sulfonylation protocol for the preparation of (E)-vinyl sulfones from of β-aryl-α,β-unsaturated carboxylic acids using sodium sulfinates and (diacetoxyiodo)benzene (PhI(OAc)<inf>2</inf>) was developed. This strategy offers a simple and expedient synthesis of (E)-vinyl sulfones bearing a wide variety of functional groups. A radical-based pathway has been proposed for this decarboxylative sulfonylation reaction. |
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Mahidol University |
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Mahidol University Praewpan Katrun Sornsiri Hlekhlai Jatuporn Meesin Manat Pohmakotr Vichai Reutrakul Thaworn Jaipetch Darunee Soorukram Chutima Kuhakarn |
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Article |
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Praewpan Katrun Sornsiri Hlekhlai Jatuporn Meesin Manat Pohmakotr Vichai Reutrakul Thaworn Jaipetch Darunee Soorukram Chutima Kuhakarn |
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Praewpan Katrun |
title |
PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
title_short |
PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
title_full |
PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
title_fullStr |
PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
title_full_unstemmed |
PhI(OAc)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: A synthesis of (E)-vinyl sulfones |
title_sort |
phi(oac)<inf>2</inf> mediated decarboxylative sulfonylation of β-aryl-α,β-unsaturated carboxylic acids: a synthesis of (e)-vinyl sulfones |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/35464 |
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1763488049037049856 |