Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones

A convenient synthesis of 5-methylene-2-cyclopentenones including Methylenomycin B involving the intramolecular acylation of α-sulfinyl carbanion followed by methylation and pyrolysis is described. © 1984.

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Main Authors:	Manat Pohmakotr, Sirirat Chancharunee
Other Authors:	Mahidol University
Format:	Article
Published:	2018
Subjects:	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
Online Access:	https://repository.li.mahidol.ac.th/handle/123456789/30584
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Institution:	Mahidol University

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spelling	th-mahidol.305842018-10-12T14:44:40Z Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones Manat Pohmakotr Sirirat Chancharunee Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A convenient synthesis of 5-methylene-2-cyclopentenones including Methylenomycin B involving the intramolecular acylation of α-sulfinyl carbanion followed by methylation and pyrolysis is described. © 1984. 2018-10-12T07:40:23Z 2018-10-12T07:40:23Z 1984-01-01 Article Tetrahedron Letters. Vol.25, No.37 (1984), 4141-4144 10.1016/S0040-4039(01)90204-7 00404039 2-s2.0-0142173082 https://repository.li.mahidol.ac.th/handle/123456789/30584 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0142173082&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 Sirirat Chancharunee Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
description	A convenient synthesis of 5-methylene-2-cyclopentenones including Methylenomycin B involving the intramolecular acylation of α-sulfinyl carbanion followed by methylation and pyrolysis is described. © 1984.
author2	Mahidol University
author_facet	Mahidol University Manat Pohmakotr Sirirat Chancharunee
format	Article
author	Manat Pohmakotr Sirirat Chancharunee
author_sort	Manat Pohmakotr
title	Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
title_short	Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
title_full	Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
title_fullStr	Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
title_full_unstemmed	Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
title_sort	intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones
publishDate	2018
url	https://repository.li.mahidol.ac.th/handle/123456789/30584
_version_	1763488714949918720

Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones

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