177903-01-4Relevant academic research and scientific papers
Chemoenzymatic synthesis of (+)-(4E,15E)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum
Ohtani, Takehiko,Kikuchi, Keiichi,Kamezawa, Makoto,Hamatani, Hideaki,Tachibana, Hojun,Totani, Tetsuzo,Naoshima, Yoshinobu
, p. 961 - 962 (1996)
An acetylenic alcohol, (+)-(4E, 15E)-docosa-4,15-dien-1-yn-3-ol 1, isolated from the marine sponge Cribrochalina vasculum, was synthesized in highly enantiomerically pure form by lipase-catalysed transesterification with Novozym 435 (Candida antarctica).
Chemoenzymatic synthesis of (+)-docosa-4,15-dien-l-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure, and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations
Morishita, Kiyoshi,Kamezawa, Makoto,Ohtani, Takehiko,Tachibana, Hojun,Kawase, Mayumi,Kishimoto, Midori,Naoshima, Yoshinobu
, p. 513 - 518 (2007/10/03)
The (4E,15Z)-, and (4￡,15￡)-isomers of (+)-docosa-4,15-dien-l-yn-3-ol 1, isolated from the marine sponge Cribroclialina vasculwn, were synthesized in highly enantiomerically pure form by lipase-mediated biotransformation with Novozym 435, and the structur
