Substrate specificity of farnesylpyrophosphate synthetase. Application to asymmetric synthesis
T Koyama, A Saito, K Ogura, S Seto
Index: Koyama, Tanetoshi; Saito, Akio; Ogura, Kyozo; Seto, Shuichi Journal of the American Chemical Society, 1980 , vol. 102, # 10 p. 3614 - 3618
Full Text: HTML
Citation Number: 38
Abstract
Abstract: Nine analogues of isopentenyl pyrophosphate (1) have been studied as substrates for pig liver farnesylpyrophosphate synthetase.(E)-3-Methylpent-3-enyl pyrophosphate (12) and its 2 isomer 13 react enzymatically with geranyl pyrophosphate (3) to give (S)-(14) and (R)-4-methylfarnesyl pyrophosphate (15), respectively. 12 and 13 also react with dimethylallyl pyrophosphate (2) to give the corresponding enantiomers of 4-methylgeranyl ...
Related Articles:
[Gruenanger, Christian U.; Breit, Bernhard Angewandte Chemie - International Edition, 2010 , vol. 49, # 5 p. 967 - 970]
[Naf, Ferdinand; Decorzant, Rene; Giersch, Wolfgang; Ohloff, Gunther Helvetica Chimica Acta, 1981 , vol. 64, # 5 p. 1387 - 1397]
[Reitz, Allen B.; Nortey, Samuel O.; Maryanoff, Bruce E.; Liotta, Dennis; Robert, Monahan Journal of Organic Chemistry, 1987 , vol. 52, # 19 p. 4191 - 4202]
[Delhaye, Laurent; Merschaert, Alain; Diker, Khalid; Houpis, Ioannis N. Synthesis, 2006 , # 9 p. 1437 - 1442]
[Wolf,H. et al. Chemische Berichte, 1976 , vol. 109, p. 41 - 57]