Login / Signup

Design of Chiral Bifunctional Dialkyl Sulfide Catalysts for Regio-, Diastereo-, and Enantioselective Bromolactonization.

Ryuichi NishiyoriAyano TsuchihashiAyaka MochizukiKazuma KanekoMasahiro YamanakaSeiji Shirakawa
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2018)
Although a wide variety of chiral organocatalysts have been developed for asymmetric transformations, effective chiral dialkyl sulfide organocatalysts remain relatively rare and under-developed, despite the potential utility of dialkyl sulfide catalysts. Herein, we report the development of chiral bifunctional dialkyl sulfide catalysts possessing a urea moiety for regio-, diastereo-, and enantioselective bromolactonization. The importance of the bifunctional design of chiral sulfide catalysts was clearly demonstrated in the present work. The roles of both the sulfide and urea moieties of the catalyst were clarified based on the results of experimental and theoretical investigation.
Keyphrases
  • highly efficient
  • metal organic framework
  • ionic liquid
  • capillary electrophoresis
  • transition metal
  • gold nanoparticles
  • human health
  • carbon dioxide