Enantioselective construction of quaternary stereogenic centers from tertiary boronic esters: Methodology and applications
Pin it down: A range of substrates that bear versatile functional groups with quaternary stereogenic centers have been prepared with very high enantioselectivity from tertiary boronic esters (see scheme; Cb=N,N-diisopropylcarbamoyl, pin=pinacolato). The preparation of allylboronic esters bearing contiguous quaternary and tertiary stereogenic centers, and applications to natural product synthesis are also reported.
Sonawane, Ravindra P.,Jheengut, Vishal,Rabalakos, Constantinos,Larouche-Gauthier, Robin,Scott, Helen K.,Aggarwal, Varinder K.
supporting information; experimental part
p. 3760 - 3763
(2011/06/22)
More Articles about upstream products of 34940-01-7