A 4(20),11(12)-taxadiene derivative was converted to hydroxylated derivativ
es by Cunninghamella elegans AS3.2033 and Cunninghamella elegans var chibae
nsis ATCC 20230. Both microorganisms led to C-1 hydroxylations and conversi
on to a C-15-hydroxylated abeo-taxane. Additional products from the two fun
gi differed: a C-14 oxidation and a trans-cis isomerization of the cinnamoy
l for one and an unprecedented hydroxylation at C-17 for the other. (C) 200
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