Ring-Opening and -Expansion of 2,2'-Biaziridine: Access to Diverse Enantiopure Linear and Bicyclic Vicinal Diamines

Date

2014

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

Source

Organic Letters

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.1021/ol502164b

Restricted until

2037-12-31