Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework
Author:
Affiliation:
1. Department of Chemistry, Wuhan University, Wuhan 430072, China kanshan@public.wh.hb.cn
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo060123n
Reference39 articles.
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4. (d) Wallbaum, S.; Martens, J.Tetrahedron: Asymmetry1992,3, 1475.
5. Asymmetric syntheses. Part IX. Reduction of ketone oximes and their O-substituted derivatives with the lithium aluminium hydride–3-O-benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose complex to give optically active amines
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