Diastereoselectivity in the Reduction of Acyclic Carbonyl Compounds with Diisopropoxytitanium(III) Tetrahydroborate-Reference-Cited by-同舟云学术

Diastereoselectivity in the Reduction of Acyclic Carbonyl Compounds with Diisopropoxytitanium(III) Tetrahydroborate

Published:1999-07-14 Issue:16 Volume:64 Page:5841-5844
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ravikumar K. S.¹,Sinha Surajit¹,Chandrasekaran S.¹

Affiliation:

1. Department of Organic Chemistry, Indian Institute of Science, Bangalore-560 012, India, and IDL-Nitro Nobel Basic Research Institute, Sankey Road, Malleswaram, Bangalore-560 012, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9902906

Reference44 articles.

1. An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction

2. Trost, B. M.; Fleming, I.Comprehensive Organic Synthesis: Selectivity,Strategy and Efficiency in Modern Organic Chemistry; Pergamon Press: Oxford, 1991; Vol. 8, p 1.

3. Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis

4. Diisopropoxytitanium(III) tetrahydroborate: a highly useful reagent for the remarkably selective 1,2-reduction of .alpha.,.beta.-unsaturated carbonyl compounds

5. Reaction of Diisopropoxytitanium(III) Tetrahydroborate with Selected Organic Compounds Containing Representative Functional Groups

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