eCite Digital Repository
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 |
UTAS 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 |
Repository Staff Only: item control page