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Cover Picture: Bidentate Chiral Bis(imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis (Angew. Chem. Int. Ed. 17/2020)
Author(s) -
Sutar Revannath L.,
Engelage Elric,
Stoll Raphael,
Huber Stefan M.
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202003880
Subject(s) - enantioselective synthesis , halogen bond , organocatalysis , aldol reaction , chemistry , denticity , halogen , catalysis , diamine , combinatorial chemistry , enantiomer , stereochemistry , polymer chemistry , organic chemistry , crystal structure , alkyl
Halogen bonding is by now established in noncovalent organocatalysis, but enantioselective applications are still very rare. In their Communication on page 6806, S. M. Huber et al. show that chiral bidentate halogen bond donors are able to differentiate the enantiomers of a diamine via NMR spectroscopy and that they can also be used to induce moderate enantioselectivity in a Mukaiyama aldol reaction. This is the first case in which enantioinduction was achieved with a “pure” halogen bond donor.