38312-11-7Relevant academic research and scientific papers
Selectivity of Candida rugosa lipase in simultaneous separation of skeletal isomers, desymmetrization, and kinetic racemate cleavage of 9-oxabicyclononanediols
Hegemann, Klaus,Schimanski, Holger,H?weler, Udo,Haufe, Günter
, p. 2225 - 2229 (2003)
The diols 2 and 3, available in one step from cycloocta-1,5-diene, are selectively acetylated at the (R)-centers using Candida rugosa lipase to give the corresponding enantiopure compounds. In contrast, the (S,S)-enantiomer of 11 is transformed under iden
