EFFICIENT PROCEDURE FOR THE PREPARATION OF CHIRAL BETA-SUBSTITUTED (E)-CROTYLSILANES - APPLICATION OF A RHODIUM(II) CATALYZED SILYLFORMYLATION OF TERMINAL ALKYNES
Nf. Jain et al., EFFICIENT PROCEDURE FOR THE PREPARATION OF CHIRAL BETA-SUBSTITUTED (E)-CROTYLSILANES - APPLICATION OF A RHODIUM(II) CATALYZED SILYLFORMYLATION OF TERMINAL ALKYNES, Tetrahedron letters, 36(48), 1995, pp. 8723-8726
Functionalized beta-substituted (E)-crotylsilanes (R)-7 and (S)-8, bea
ring an alkyl or aryl group adjacent to the stereogenic C-Si center ha
ve been synthesized in an efficient four-step procedure initiated with
a regio- and stereoselective silylformylation of a terminal alkyne ca
talyzed by dirhodium(II) perfluorobutyrate.