Regio- and stereoselectivity of the formation of 1,3-oxazolidines in the reaction of l-ephedrine with phenylglyoxal. Unexpected rearrangement of 2-benzoyl-3,4-dimethyl-5-phenyl-1,3-oxazolidine to 4,5-dimethyl-3,6-diphenylmorpholin-2-one.-Reference-Cited by-同舟云学术

Regio- and stereoselectivity of the formation of 1,3-oxazolidines in the reaction of l-ephedrine with phenylglyoxal. Unexpected rearrangement of 2-benzoyl-3,4-dimethyl-5-phenyl-1,3-oxazolidine to 4,5-dimethyl-3,6-diphenylmorpholin-2-one.

Published:1996-11 Issue:45 Volume:37 Page:8223-8226
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Polyak Felix,Dorofeeva Tatiana,Zelchans Gunars,Shustov Gennady

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

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2. Moore, B.S.; Urban, F.J. U.S. US 5,149,821, 1992. C.A.1993.118, 147462r.

3. Asymmetric synthesis via nor-ephedrine derived 2-alkenyloxazolidines

4. Influence of the ester group during the enantioselective methylation of α-aldehyde esters via their chiral oxazolidine derivatives

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