Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.

(±)-Pentenomycin I and (±)-epipentenomycin I were synthesized, starting from methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate. The key reaction involved the intramolecular acylation of α-sulfinyl carbanion and pyrolysis of the resulting product. © 1991.

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Main Authors:	Manat Pohmakotr, Supatara Popuang
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/123456789/21993
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Institution:	Mahidol University

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spelling	th-mahidol.219932018-08-10T15:36:38Z Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I. Manat Pohmakotr Supatara Popuang Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics (±)-Pentenomycin I and (±)-epipentenomycin I were synthesized, starting from methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate. The key reaction involved the intramolecular acylation of α-sulfinyl carbanion and pyrolysis of the resulting product. © 1991. 2018-08-10T08:30:42Z 2018-08-10T08:30:42Z 1991-01-07 Article Tetrahedron Letters. Vol.32, No.2 (1991), 275-278 10.1016/0040-4039(91)80874-6 00404039 2-s2.0-0026068713 https://repository.li.mahidol.ac.th/handle/123456789/21993 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026068713&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 Supatara Popuang Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
description	(±)-Pentenomycin I and (±)-epipentenomycin I were synthesized, starting from methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate. The key reaction involved the intramolecular acylation of α-sulfinyl carbanion and pyrolysis of the resulting product. © 1991.
author2	Mahidol University
author_facet	Mahidol University Manat Pohmakotr Supatara Popuang
format	Article
author	Manat Pohmakotr Supatara Popuang
author_sort	Manat Pohmakotr
title	Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
title_short	Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
title_full	Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
title_fullStr	Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
title_full_unstemmed	Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.
title_sort	intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin i and (±)-epipentenomycin i.
publishDate	2018
url	https://repository.li.mahidol.ac.th/handle/123456789/21993
_version_	1763487639227334656

Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.

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