Stereochemical aspects of the bioreduction of the conjugated double bond of perillaldehyde
G Fronza, C Fuganti, M Pinciroli, S Serra
Index: Fronza, Giovanni; Fuganti, Claudio; Pinciroli, Matteo; Serra, Stefano Tetrahedron Asymmetry, 2004 , vol. 15, # 19 p. 3073 - 3077
Full Text: HTML
Citation Number: 13
Abstract
A study on the regioselective reduction of the conjugate double bond of perillaldehyde is described. The chemical reduction of this substrate was investigated in order to provide a straightforward access to the relevant natural flavour, dihydroperillaldehyde. The biological reduction of both natural (S)-(−)-perillaldehyde and synthetic (R)-(+)-perillaldehyde was accomplished by means of fermenting baker's yeast. The latter microorganism converted, ...
Related Articles:
[Barrero, Alejandro F.; Herrador, M. Mar; Quilez Del Moral, Jose F.; Arteaga, Pilar; Arteaga, Jesus F.; Dieguez, Horacio R.; Sanchez, Elena M. Journal of Organic Chemistry, 2007 , vol. 72, # 8 p. 2988 - 2995]
[Wang, Qian; Fan, Shi Yan; Wong, Henry N. C.; Li, Zhong; Fung, Bing M.; Twieg, Robert J.; Nguyen, Huu Tinh Tetrahedron, 1993 , vol. 49, # 3 p. 619 - 638]
[Wang, Qian; Fan, Shi Yan; Wong, Henry N. C.; Li, Zhong; Fung, Bing M.; Twieg, Robert J.; Nguyen, Huu Tinh Tetrahedron, 1993 , vol. 49, # 3 p. 619 - 638]
[Miyazawa, Mitsuo; Shindo, Masaki; Shimada, Tsutomu Chemical Research in Toxicology, 2002 , vol. 15, # 1 p. 15 - 20]
[Mcgraw, Gerald W.; Hemingway, Richard W.; Ingram Jr., Leonard L.; Canady, Catherine S.; Mcgraw, William B. Environmental Science and Technology, 1999 , vol. 33, # 22 p. 4029 - 4033]