Regioselective reductive transamination of peptidic amides enabled by a dual Zr(IV)

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Regioselective reductive transamination of peptidic amides enabled by a dual Zr(IV)–H catalysis

Published:2023-04 Issue:4 Volume:9 Page:869-880
ISSN:2451-9294
Container-title:Chem
language:en
Short-container-title:Chem

Author:

Tang Jian-Tao,Gan Yu,Li Xuejiao,Ye Baihua

Publisher

Elsevier BV

Subject

Materials Chemistry,Biochemistry (medical),General Chemical Engineering,Environmental Chemistry,Biochemistry,General Chemistry

Reference94 articles.

1. Nonclassical routes for amide bond formation;de Figueiredo;Chem. Rev.,2016

2. Acyclic twisted amides;Meng;Chem. Rev.,2021

3. The Staudinger ligation;Bednarek;Chem. Rev.,2020

4. Peptoids and polypeptoids at the frontier of supra- and macromolecular engineering;Gangloff;Chem. Rev.,2016

5. Analysis of the reactions used for the preparation of drug candidate molecules;Carey;Org. Biomol. Chem.,2006

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