The biocatalytic hydrolysis of the (+/-)-2,3-disubstituted cis-chloroalkyl
epoxides 1a and 2a using resting cells of Rhodococcus sp. did not give the
corresponding chloroalkyl vic-diols 1b, and 2b, respectively, but furnished
the rearranged products (2R,3R)-1c and (2R,3R)-2c in high e.e. as the sole
products via an enzyme-triggered enantio-convergent cascade-reaction. (C)
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