Bulletin of the Chemical Society of Japan p. 1601 - 1602 (1985)
Update date:2022-08-11
Topics:
SOAI, Kenso
OHI, Kazumi
Reduction of relatively conformationally rigid cyclic ketones with sodium borohydride was examined in a mixed solvent of tetrahydrofuran (THF)and methanol (MeOH) with varying the ratio of the components.The highest stereoselectivities of the reductions were observed in the mixed solvent, and not in each individual solvent.
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