Enantioselective synthesis of epoxides and aziridines by asymmetric methylidene transfer from a sulfimide to carbonyl compounds and imines
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 0300-922XFull text not available from this repository.
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|
|Date:||21 October 1998|
|Number of Pages:||5|
|Page Range:||pp. 3399-3403|
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