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Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions

Citation

Carballares, S and Craig, D and Hyland, CJT and Lu, P and Mathie, T and White, AJP, Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions, Chemical Communications, 2009, (4) pp. 451-453. ISSN 1359-7345 (2009) [Refereed Article]

DOI: doi:10.1039/b815971h

Abstract

The highly regioselective, stereospecific ring-opening of trisubstituted N-tosylaziridines possessing vinyl and hydroxymethyl groups by sulfone-and sulfide-stablised carbanions is reported.

Item Details

Item Type:Refereed Article
Research Division:Chemical Sciences
Research Group:Organic Chemistry
Research Field:Organic Chemical Synthesis
Objective Division:Expanding Knowledge
Objective Group:Expanding Knowledge
Objective Field:Expanding Knowledge in the Chemical Sciences
Author:Hyland, CJT (Dr Chris Hyland)
ID Code:72660
Year Published:2009
Web of Science® Times Cited:8
Deposited By:Chemistry
Deposited On:2011-08-30
Last Modified:2012-03-06
Downloads:0

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