γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides

Lithiated 2-buten-4-olide was found to react with aromatic aldehydes regioselectively at γ-position to provide 4-(1-aryl-1-hydroxymethyl)-2- buten-4-olides which could be readily converted into the corresponding (Z)- γ-arylidenebutenolides.

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Main Authors: Manat Pohmakotr, Patoomratana Tuchinda, Pornchai Premkaisorn, Vichai Reutrakul
其他作者: Mahidol University
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出版: 2018
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在線閱讀:https://repository.li.mahidol.ac.th/handle/123456789/18292
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spelling th-mahidol.182922018-07-04T15:19:24Z γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides Manat Pohmakotr Patoomratana Tuchinda Pornchai Premkaisorn Vichai Reutrakul Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Lithiated 2-buten-4-olide was found to react with aromatic aldehydes regioselectively at γ-position to provide 4-(1-aryl-1-hydroxymethyl)-2- buten-4-olides which could be readily converted into the corresponding (Z)- γ-arylidenebutenolides. 2018-07-04T08:03:03Z 2018-07-04T08:03:03Z 1998-09-10 Article Tetrahedron. Vol.54, No.37 (1998), 11297-11304 10.1016/S0040-4020(98)00669-3 00404020 2-s2.0-0032505193 https://repository.li.mahidol.ac.th/handle/123456789/18292 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032505193&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Manat Pohmakotr
Patoomratana Tuchinda
Pornchai Premkaisorn
Vichai Reutrakul
γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
description Lithiated 2-buten-4-olide was found to react with aromatic aldehydes regioselectively at γ-position to provide 4-(1-aryl-1-hydroxymethyl)-2- buten-4-olides which could be readily converted into the corresponding (Z)- γ-arylidenebutenolides.
author2 Mahidol University
author_facet Mahidol University
Manat Pohmakotr
Patoomratana Tuchinda
Pornchai Premkaisorn
Vichai Reutrakul
format Article
author Manat Pohmakotr
Patoomratana Tuchinda
Pornchai Premkaisorn
Vichai Reutrakul
author_sort Manat Pohmakotr
title γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
title_short γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
title_full γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
title_fullStr γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
title_full_unstemmed γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
title_sort γ-regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: a simple synthesis of γ-arylidenebutenolides
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/18292
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