6388-22-3Relevant articles and documents
Microbial oxygenation of cycloheptyl-N-phenylcarbamate and (±)-trans-2-fluorocycloheptyl-N-phenylcarbamate with Beauveria bassiana
Pietz, Sylke,Froehlich, Roland,Haufe, Guenter
, p. 17055 - 17066 (1997)
The title biotransformation of 1 gave trans-4-hydroxycyclohept-1-yl-carbamate (3, 10%, 62% ee), its consecutive ketone 5 (12%) and the racemic cis-isomer 4 (1.8%). Similarly, the racemic trans-2-fluoro analogue 2 yielded mainly four optically active alcoh