125284-17-5Relevant articles and documents
The Enantiomeric Purity of (S)- and (R)-4-Methylfarnesols Synthesized from Artifical Substrates by Means of a Farnesyl Diphosphate Synthase Reaction
Ohnuma, Shin-ichi,Koyama, Tanetoshi,Ogura, Kyozo
, p. 2742 - 2744 (2007/10/02)
Both (S)- and (R)-4-methylfarnesols, synthesized respectively from (E)- and (Z)-3-methyl-3-pentenyl diphosphates by means of farnesyl diphosphate synthase reactions, were demonstrated to be of almost 100percent enantiomeric purity.
UNDECAPRENYL DIPHOSPHATE SYNTHASE REACTION WITH ARTIFICAL SUBSTRATE HOMOLOGUES ------- NOVEL BEHAVIOR IN THE TERMINATION OF PRENYL CHAIN ELONGATION
Ohnuma, Shin-ichi,Ito, Michio,Koyama, Tanetoshi,Ogura, Kyozo
, p. 6145 - 6160 (2007/10/02)
(E)-3-Methyl-3-pentenyl diphosphate acted as an artifical homoallylic substrate in the reaction with several allylic diphosphates catalyzed by undecaprenyl diphosphate synthase of Bacillus subtilis.The synthase reaction with the artificial substrate proceeded in the same stereochemical manner as that with the natural homoallylic substrate, isopentenyl diphosphate, but it had a full stop at the stage where a single condensation of the C6-homologue with an allylic primer is completed to form a chiral prenyl diphosphate with an extra methyl group at the 4-position.Allylic diphosphates that each have an extra methyl group at the 4-position were not accepted as substrates for this enzyme even when isopentenyl diphosphate was the homoallylic substrate.
