Asymmetric Reductions Involving Borohydrides: A Practical Asymmetric Reduction of Ketones Mediated by (l)-TarB−NO2: A Chiral Lewis Acid-Reference-Cited by-同舟云学术

Asymmetric Reductions Involving Borohydrides: A Practical Asymmetric Reduction of Ketones Mediated by (l)-TarB−NO2: A Chiral Lewis Acid

Published:2006-08-01 Issue:5 Volume:10 Page:949-958
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Kim Jinsoo¹,Suri Jeff T.¹,Cordes David B.¹,Singaram Bakthan¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Santa Cruz, 1156 High Street, Santa Cruz, California 95064, U.S.A., GluMetrix, Inc. 15375 Barranca Parkway, Suite I-108, Irvine, California 92618, U.S.A., and Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op060079d

Reference63 articles.

1. Spatial Arrangement and Preparative Organic Synthesis

2. Organic Synthesis—Where now?

3. AsymmetricSynthesisofNaturalProducts; Kosikinen, A.; John Wiley & Sons Ltd: New York, 1993.

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