Diastereoselective Additions of Allylmagnesium Reagents to α-Substituted Ketones When Stereochemical Models Cannot Be Used

Author:

Bartolo Nicole D.1ORCID,Demkiw Krystyna M.1ORCID,Valentín Elizabeth M.2,Hu Chunhua T.1ORCID,Arabi Alya A.34ORCID,Woerpel K. A.1ORCID

Affiliation:

1. Department of Chemistry, New York University, 100 Washington Square East, New York, NY 10003, United States

2. St. Mary’s College of California, 1928 St. Marys Road, Moraga, California 94575, United States

3. Biochemistry Department, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, United Arab Emirates

4. Centre for Computational Science, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom

Funder

Division of Chemistry

NIH Office of the Director

National Institute of General Medical Sciences

Division of Materials Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference82 articles.

1. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

2. Around and beyond Cram's Rule

3. Huryn, D. M. Carbanions of Alkali and Alkaline-Earth Cations: (II) Selectivity of Carbonyl Addition Reactions. In Comprehensive Organic Synthesis II; Knochel, P., Molander, G. A., Eds. Elsevier: Amsterdam, 2014; p 1.

4. (II) Selectivity of Carbonyl Addition Reactions. In Comprehensive Organic Synthesis II; Knochel, P., Molander, G. A., Eds. Elsevier: Amsterdam, 2014; p 1.

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