Catalytic Enantioselective Hydrostannation of Cyclopropenes

Abstract
The first examples of catalytic enantioselective hydrostannation of the CC double bond of cyclopropenes has been demonstrated. This method allows for the efficient synthesis of 2,2-disubstituted cyclopropylstannanes with high degrees of diastereo- and enantioselectivity. The facial selectivity of this reaction is entirely controlled by steric factors. A variety of functional groups at C-3 of the cyclopropenes were tolerated.

This publication has 15 references indexed in Scilit: