Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107507
Title: Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
Authors: Ribeiro, João L. P. 
Alves, Cláudia 
Cardoso, Ana L. 
Lopes, Susana M. M. 
Pinho e Melo, Teresa M. V. D. 
Keywords: Chiral amines; asymmetric reduction; enantioselective reduction; diastereoselective reduction; oximes; chiral hydroxylamines; hydrazones; chiral hydrazines
Issue Date: 2021
Publisher: Bentham Science
Project: UIDB/00313/2020 
UIDP/QUI/00313/2020 
PD/BD/143160/2019 
PD/BD/143159/2019 
Serial title, monograph or event: Current Organic Chemistry
Volume: 25
Issue: 19
Abstract: The asymmetric reduction of oximes and hydrazones is an attractive and versatile strategy for the synthesis of chiral amines, which are valuable building blocks in organic synthesis. This review summarizes the relevant developments, made in the last decade, on the enantioselective and diastereoselective reduction of oximes and hydrazones involving metal-catalyzed hydrogenation/hydrogenolysis reactions, hydride donor reactions, and electrochemical reactions.
URI: https://hdl.handle.net/10316/107507
ISSN: 13852728
DOI: 10.2174/1385272825666210706151631
Rights: embargoedAccess
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais

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