Synlett p. 1297 - 1299 (1997)
Update date:2022-08-25
Topics:
Konegawa, Tadayoshi
Ohtsuka, Yoshikazu
Ikeda, Hajime
Sugai, Takeshi
Ohta, Hiromichi
Both enantiomers (>95% e.e.) of 2-methyl-3,4-pentadien-1-ol, a chiral building block possessing a terminal allenyl group were prepared via the two-stage enzymatic kinetic resolution, i.e., a sequence of lipase-catalyzed acetylation (Pseudomonas cepacia) and hydrolysis (Candida antarctica).
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