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Exploiting Octahedral Stereocenters: From Enzyme Inhibition to Asymmetric Photoredox Catalysis
Author(s) -
Meggers Eric
Publication year - 2017
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201612516
Subject(s) - stereocenter , chemistry , octahedron , catalysis , enantioselective synthesis , asymmetric hydrogenation , combinatorial chemistry , stereochemistry , biocatalysis , photoredox catalysis , enzyme , organic chemistry , photocatalysis , reaction mechanism , crystal structure
A simple concept , namely exploiting the structural and stereochemical complexity of octahedral metal complexes, can have unexpected impact in different areas of chemical research, from medicinal chemistry and chemical biology to asymmetric catalysis and photoredox chemistry.