Organometallics, 19 (5), 944 -946, 2000. 10.1021/om990917a S0276-7333(99)00917-6
Web Release Date: February 4, 2000

Copyright © 2000 American Chemical Society

Efficient Catalytic Deoxygenation of Epoxides Using [Tris(3,5-dimethylpyrazolyl)hydridoborato]rhenium Oxides

Kevin P. Gable* and Eric C. Brown

Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003

Received November 22, 1999

Abstract:

In situ reduction of Tp'ReO3 (Tp' = tris(3,5-dimethylpyrazolyl)hydridoborate) using triphenylphosphine or triethyl phosphite allows generation of a reduced rhenium species that catalyzes efficient O atom transfer from epoxides to the stoichiometric phosphorus reductant at 75-105 C. The reaction is stereospecific and proceeds most rapidly with cis- vs trans-alkenes. The choice of ligand is shown to impart advantages to design of the catalytic cycle.


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