An unusual matrix of stereocomplementarity in the hydroxylation of monohydroxy fatty acids catalysed by cytochrome P-450 from Bacillus megaterium with potential application in biotransformations
F. Ahmed et al., An unusual matrix of stereocomplementarity in the hydroxylation of monohydroxy fatty acids catalysed by cytochrome P-450 from Bacillus megaterium with potential application in biotransformations, CHEM COMMUN, (20), 1999, pp. 2049-2050
Cytochrome P-450 from Bacillus megaterium catalyses the diastereoselective
hydroxylations of 13-hydroxymyristic acid, to predominantly erythro-12,13-d
ihydroxymyristic acid, and of 12-hydroxymyristic acid to give predominantly
threo-12,13-dihydroxymyristic acid, in reactions that are stereocomplement
ary and with considerable potential application in biotransformations.