Solvent-Induced Chirality in the Hydroboration of Ketones
Keyword(s):
The influence of the systematic variation of chiral solvents and of diverse Lewis acids on the asymmetric induction of the hydroboration of acetophenone has been studied. None of the solvents used could surpass lactic acid methyl ester, and for the Lewis acids, ZnCl2 and ZnI2 showed positive effects on the enantiomeric excess (ee) and the conversion. Also, the effect of the substrate structure was investigated by comparing the conversion and ee of eight different ketones. Apparently, the achievable asymmetric induction was higher with aromatic ketones.
2011 ◽
Vol 56
(14)
◽
pp. 5137-5141
◽
Keyword(s):
2008 ◽
Keyword(s):
2015 ◽
Keyword(s):
2015 ◽
Keyword(s):
Keyword(s):