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

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type 01 Jan 2021 English Publisher:Royal Society of Chemistry (RSC)Journal:Chemical Science, volume 12, pages 5,430-5,437 (issn: 2041-6520, eissn: 2041-6539, Copyright policy )
Authors: Andrey Shatskiy; Anton Axelsson; Elena V. Stepanova; Jian-Quan Liu; Azamat Z. Temerdashev; Bhushan P. Kore; Björn Blomkvist; +3 Authors

doi: 10.1039/d1sc00658d

pmid: 34168785

pmc: PMC8179686

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

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.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
41
Top 10%
Top 10%
Top 1%
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