Enantioselective Addition of Boronates to Acyl Imines Catalyzed by Chiral Biphenols
JA Bishop, S Lou, SE Schaus
Index: Bishop, Joshua A.; Lou, Sha; Schaus, Scott E. Angewandte Chemie, International Edition, 2009 , vol. 48, # 24 p. 4337 - 4340
Full Text: HTML
Citation Number: 38
Abstract
Abstract On the big screen: A chiral biphenol catalyst screening protocol was developed for the rapid identification of enantioselective nucleophilic boronate reactions with acyl imines (see scheme). The approach successfully identified a unique catalyst for the reaction of aryl, vinyl, and alkynyl boronates. Mechanistic studies demonstrate boronate ligand exchange with the catalyst is necessary for activation towards nucleophilic addition.
Related Articles:
[Angewandte Chemie - International Edition, , vol. 41, # 19 p. 3692 - 3694]
[Jagt, Richard B. C.; Toullec, Patrick Y.; Geerdink, Danny; De Vries, Johannes G.; Feringa, Ben L.; Minnaard, Adriaan J. Angewandte Chemie - International Edition, 2006 , vol. 45, # 17 p. 2789 - 2791]
Synthesis and applications of chiral organoboranes generated from sulfonium ylides
[Journal of the American Chemical Society, , vol. 127, # 6 p. 1642 - 1643]
[Angewandte Chemie - International Edition, , vol. 41, # 19 p. 3692 - 3694]
[Ghislieri, Diego; Green, Anthony P.; Pontini, Marta; Willies, Simon C.; Rowles, Ian; Frank, Annika; Grogan, Gideon; Turner, Nicholas J. Journal of the American Chemical Society, 2013 , vol. 135, # 29 p. 10863 - 10869]