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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 |
| 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 |
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