I. Ryu et al., HYDROXYMETHYLATION OF ORGANIC HALIDES - EVALUATION OF A CATALYTIC-SYSTEM INVOLVING A FLUOROUS TIN HYDRIDE REAGENT FOR RADICAL CARBONYLATION, Tetrahedron letters, 38(45), 1997, pp. 7883-7886
Hydroxymethylation of organic halides 2 using a catalytic amount of fl
uorous tin hydride 1, CO, and NaBH3CN as a reducing agent, proceeded s
moothly to give one-carbon homologated alcohols 5 in good yields. Thre
e phase workup (water-dichloromethane-perfluorohexane) was convenientl
y performed for the separation of 1 and 5. (C) 1997 Elsevier Science L
td.