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Enantioselective synthesis of epoxides and aziridines by asymmetric methylidene transfer from a sulfimide to carbonyl compounds and imines
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UNSPECIFIED (1998) Enantioselective synthesis of epoxides and aziridines by asymmetric methylidene transfer from a sulfimide to carbonyl compounds and imines. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 (20). pp. 3399-3403. ISSN 0300-922X
Full text not available from this repository.Abstract
The sodium salt of sulfimide 2 is a useful asymmetric methylidene transfer agent for the synthesis of enantiomerically enriched epoxides and aziridines. Moderate enantioselectivities are observed with a broad range of carbonyl compounds and with imines. An enantiomerically enriched beta-adrenoreceptor agonist analogue was prepared using the new method.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 |
| Publisher: | ROYAL SOC CHEMISTRY |
| ISSN: | 0300-922X |
| Date: | 21 October 1998 |
| Number: | 20 |
| Number of Pages: | 5 |
| Page Range: | pp. 3399-3403 |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/15239 |
Data sourced from Thomson Reuters' Web of Knowledge
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