Ring-Opening and -Expansion of 2,2'-Biaziridine: Access to Diverse Enantiopure Linear and Bicyclic Vicinal Diamines
Date
Authors
Bailey, Stephen J.
Wales, Steven M
Willis, Anthony
Keller, Paul
Journal Title
Journal ISSN
Volume Title
Publisher
American Chemical Society
Abstract
The chiral pool-derived 1,1′-ditosyl-2,2′-biaziridine has been established as a valuable building block for the divergent synthesis of enantiopure vicinal diamines. Efficient procedures for the regioselective ring opening of the biaziridine with oxyge
Description
Keywords
Citation
Collections
Source
Organic Letters
Type
Book Title
Entity type
Access Statement
License Rights
Restricted until
2037-12-31