STEREOSPECIFIC INTRAMOLECULAR PROTON-TRANSFER IN THE CYCLIZATION OF GERANYLGERANYL DIPHOSPHATE TO (-)-ABIETADIENE CATALYZED BY RECOMBINANT CYCLASE FROM GRAND FIR (ABIES GRANDIS)
Mm. Ravn et al., STEREOSPECIFIC INTRAMOLECULAR PROTON-TRANSFER IN THE CYCLIZATION OF GERANYLGERANYL DIPHOSPHATE TO (-)-ABIETADIENE CATALYZED BY RECOMBINANT CYCLASE FROM GRAND FIR (ABIES GRANDIS), Chemical communications, (1), 1998, pp. 21-22
The cyclization-rearrangement of deuterated geranylgeranyl diphosphate
(GGPP) and (+)-copalyl diphosphate (CPP) catalyzed by recombinant (-)
-abietadiene synthase from grand fir proceeds with intramolecular prot
on transfer from C-19 of GGPP, and from the C-17 pro-E position of CPP
, to form the C-16 pro-S methyl group of (-)-abietadiene.