Synthesis of optically-active benzylic amines; asymmetric reduction of ketoxime ethers with chiral oxazaborolidines-Reference-Cited by-同舟云学术

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Synthesis of optically-active benzylic amines; asymmetric reduction of ketoxime ethers with chiral oxazaborolidines

Published:2001-08 Issue:15 Volume:12 Page:2185-2189
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fontaine Evelyne,Namane Claudie,Meneyrol Jérôme,Geslin Michel,Serva Laurence,Roussey Eliane,Tissandié Stéphanie,Maftouh Mohamed,Roger Pierre

Publisher

Elsevier BV

Subject

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

Reference9 articles.

1. Asymmetric syntheses with chiral oxazaborolidines

2. Asymmetric reduction of aromatic ketones with chiral alkoxy-amineborane complexes

3. Asymmetric synthesis using chirally modified borohydrides. Part 3. Enantioselective reduction of ketones and oxime ethers with reagents prepared from borane and chiral amino alcohols

4. Asymmetric reduction of oxime ethers. Distinction of anti and syn isomers leading to enantiomeric amines.

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1. Asymmetric hydrogenation of TIPS-protected oximes with chiral boranes;Organic & Biomolecular Chemistry;2022

2. Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities;Chemistry – A European Journal;2021-12-22

3. Formation of Amines from Aldehydes, Ketones, and Derivatives;Comprehensive Organic Transformations;2018-02-28

4. Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives;Tetrahedron: Asymmetry;2016-04

5. B(C6F5)3-Catalyzed Hydrogenation of Oxime Ethers without Cleavage of the NO Bond;Angewandte Chemie International Edition;2014-10-05

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