Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones

A general method for the preparation of 5-substituted Δ2-cyclopentenones via the intramolecular acylation of αot-sulfinyl carbanions has been demonstrated. © 1984.

Saved in:
Bibliographic Details
Main Authors: Manat Pohmakotr, Pranee Phinyocheep
Other Authors: Mahidol University
Format: Article
Published: 2018
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/30579
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University
id th-mahidol.30579
record_format dspace
spelling th-mahidol.305792018-10-12T14:44:39Z Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones Manat Pohmakotr Pranee Phinyocheep Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A general method for the preparation of 5-substituted Δ2-cyclopentenones via the intramolecular acylation of αot-sulfinyl carbanions has been demonstrated. © 1984. 2018-10-12T07:40:16Z 2018-10-12T07:40:16Z 1984-01-01 Article Tetrahedron Letters. Vol.25, No.21 (1984), 2249-2252 10.1016/S0040-4039(01)80224-0 00404039 2-s2.0-0343046278 https://repository.li.mahidol.ac.th/handle/123456789/30579 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0343046278&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
Pranee Phinyocheep
Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
description A general method for the preparation of 5-substituted Δ2-cyclopentenones via the intramolecular acylation of αot-sulfinyl carbanions has been demonstrated. © 1984.
author2 Mahidol University
author_facet Mahidol University
Manat Pohmakotr
Pranee Phinyocheep
format Article
author Manat Pohmakotr
Pranee Phinyocheep
author_sort Manat Pohmakotr
title Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
title_short Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
title_full Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
title_fullStr Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
title_full_unstemmed Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones
title_sort intramolecular acylation of α-sulfinyl carbanion: a new general route to 5-substituted δ<sup>2</sup>cyclopentenones
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/30579
_version_ 1763492195647619072