Work

Stereoselective synthesis of unnatural α-amino acid derivatives through photoredox catalysis

Year: 2021

Type: article

Abstract: A protocol for stereoselective C-radical addition to a chiral glyoxylate-derived N -sulfinyl imine was developed through visible light-promoted photoredox catalysis, providing a convenient method for the synthesis of unnatural α-amino acids.

Source: Chemical Science

DOI: 10.1039/d1sc00658d

Authors: Andrey Shatskiy, Anton Axelsson, Elena V. Stepanova, Jian-Quan Liu, Azamat Z. Temerdashev, Bhushan P. Kore, Björn Blomkvist, James M. Gardner, Peter Dinér, Markus D. Kärkäs

Institutions: KTH Royal Institute of Technology, Russian Academy of Sciences, Tomsk Polytechnic University, N.D. Zelinsky Institute of Organic Chemistry, Kuban State University

Language: English

Topic: Radical Photochemical Reactions

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: diamond

Funders: Tomsk Polytechnic University, Wenner-Gren Stiftelserna, Svenska Forskningsrådet Formas, Carl Tryggers Stiftelse för Vetenskaplig Forskning, Ministry of Education and Science of the Russian Federation, Stiftelsen Olle Engkvist Byggmästare, Kungliga Tekniska Högskolan, Vetenskapsrådet, Magnus Bergvalls Stiftelse

Awards: G1234549773, Photons as a reagent in organic synthesis, Kemisk syntes med synligt ljus, G807642875

OpenAlex ID: W3134871268

FWCI: 4.897

Cites: 64

Cited by: 73

Related to: 10