Highly enantioselective carbonyl reduction with borane catalyzed by chiral spiroborate esters derived from chiral 1,2-aminoalcohols-Reference-Cited by-同舟云学术

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Highly enantioselective carbonyl reduction with borane catalyzed by chiral spiroborate esters derived from chiral 1,2-aminoalcohols

Published:2006-01 Issue:1 Volume:17 Page:112-115
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Stepanenko Viatcheslav,Ortiz-Marciales Margarita,Correa Wildeliz,De Jesús Melvin,Espinosa Sandraliz,Ortiz Lymaris

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference20 articles.

1. Reductions by the Alumino- and Borohydrides in Organic Synthesis;Seyden-Penne,1997

2. Enantioselective reductions by chirally modified alumino- and borohydrides

3. Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances

4. Asymmetric synthesis using chirally modified borohydrides. Part 1. Enantioselective reduction of aromatic ketones with the reagent prepared from borane and (S)-valinol

5. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method

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3. Enantioselective Reduction of Ketones and Synthesis of 2-Methyl-2,3-dihydro-1-benzofuran Catalyzed by Chiral Spiroborate Ester;Russian Journal of Organic Chemistry;2021-04

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