Enzymic condensation of 3-methyl-2-alkenyl pyrophosphates with isopentenyl pyrophosphate
K Ogura, T Nishino, T Koyama…
Index: Ogura,K. et al. Journal of the American Chemical Society, 1970 , vol. 92, p. 6036 - 6041
Full Text: HTML
Citation Number: 66
Abstract
Abstract: The substrate specificity of farnesyl pyrophosphate synthetase of pumpkin fruit was studied by using synthetic 3-methyl-2-alkenyl pyrophosphates. cis-3-Methyl-2-hexenyl pyrophosphate (19) reacted enzymically with isopentenyl pyrophosphate (1) as well as the trans isomer 12, and even cis-3-methyl-2-heptenyl pyrophosphate (20) was reactive, though far less reactive than its trans isomer 13. However, cis-3-methyl-2-octenyl pyrophosphate ( ...
Related Articles:
[Kapferer, Tobias; Brueckner, Reinhard; Herzig, Axel; Koenig, Wilfried A. Chemistry - A European Journal, 2005 , vol. 11, # 7 p. 2154 - 2162]
[Homsi, Fadi; Rousseau, Gerard Journal of Organic Chemistry, 1999 , vol. 64, # 1 p. 81 - 85]
[Homsi, Fadi; Rousseau, Gerard Journal of Organic Chemistry, 1999 , vol. 64, # 1 p. 81 - 85]
[Okukado,N.; Negishi,E. Tetrahedron Letters, 1978 , # 27 p. 2357 - 2360]