A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines

The reaction of lithio α-chloromethyl phenyl sulfone with imines gave aziridines in good yields. The resulting aziridines were alkylated and underwent the 1,3-dipolar cycloaddition with dimethylacetylene dicarboxylate to give pyrroles in excellent yields. © 1984.

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Main Authors:	Vichai Reutrakul, Vichukorn Prapansiri, Chitchanun Panyachotipun
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/123456789/30577
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Institution:	Mahidol University

id	th-mahidol.30577
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spelling	th-mahidol.305772018-10-12T14:44:38Z A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines Vichai Reutrakul Vichukorn Prapansiri Chitchanun Panyachotipun Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics The reaction of lithio α-chloromethyl phenyl sulfone with imines gave aziridines in good yields. The resulting aziridines were alkylated and underwent the 1,3-dipolar cycloaddition with dimethylacetylene dicarboxylate to give pyrroles in excellent yields. © 1984. 2018-10-12T07:40:15Z 2018-10-12T07:40:15Z 1984-01-01 Article Tetrahedron Letters. Vol.25, No.18 (1984), 1949-1952 10.1016/S0040-4039(01)90084-X 00404039 2-s2.0-0000004487 https://repository.li.mahidol.ac.th/handle/123456789/30577 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0000004487&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 Vichai Reutrakul Vichukorn Prapansiri Chitchanun Panyachotipun A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
description	The reaction of lithio α-chloromethyl phenyl sulfone with imines gave aziridines in good yields. The resulting aziridines were alkylated and underwent the 1,3-dipolar cycloaddition with dimethylacetylene dicarboxylate to give pyrroles in excellent yields. © 1984.
author2	Mahidol University
author_facet	Mahidol University Vichai Reutrakul Vichukorn Prapansiri Chitchanun Panyachotipun
format	Article
author	Vichai Reutrakul Vichukorn Prapansiri Chitchanun Panyachotipun
author_sort	Vichai Reutrakul
title	A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
title_short	A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
title_full	A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
title_fullStr	A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
title_full_unstemmed	A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
title_sort	new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines
publishDate	2018
url	https://repository.li.mahidol.ac.th/handle/123456789/30577
_version_	1763489296225927168

A new method for the synthesis of 2-phenylsulfonylaziridines via the reaction of α-halosulfonyl carbanion to imines

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