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LiClO4-catalyzed cleavage of aziridines with thiols: A facile synthesis of β-aminosulfides

Paper ID Volume ID Publish Year Pages File Format Full-Text
53174 46917 2006 4 PDF Available
Title
LiClO4-catalyzed cleavage of aziridines with thiols: A facile synthesis of β-aminosulfides
Abstract

Aziridines react smoothly with thiols in the presence of catalytic amount of lithium perchlorate under essentially mild and neutral reaction conditions to afford the corresponding β-aminosulfides in high yields with high regioselectivity.

Keywords
Lithium perchlorate; Aziridines; Thiols; β-Aminosulfides
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LiClO4-catalyzed cleavage of aziridines with thiols: A facile synthesis of β-aminosulfides
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 7, Issue 10, October 2006, Pages 807–810
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
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Price was $35.95
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