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Synlett 2006(2): 181-193
DOI: 10.1055/s-2006-926220
DOI: 10.1055/s-2006-926220
ACCOUNT
© Georg Thieme Verlag Stuttgart · New York
Towards Reaction Selectivities of Imines and Aziridines
Further Information
Received
31 July 2005
Publication Date:
24 January 2006 (online)
Publication History
Publication Date:
24 January 2006 (online)
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Abstract
Several simple and convenient transformations of imines and aziridines under mild conditions have been developed, rendering access to several kinds of β-amino derivatives, α-amino nitriles and phosphonates, aziridines, and conjugated dienes from imines and aziridines under neutral and metal-free conditions very conveniently. High stereoselectivities are realized in most reactions based upon mechanistic considerations.
Key words
transformations - imines - aziridines - mild conditions
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References and Notes
Current address: Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, P. R. of China