TY - JOUR
T1 - Biochemical preparation of optically active 4-hydroxy-β-ionone and its transformation to (S)-6-hydroxy-α-ionone
AU - Kakeya, Hideaki
AU - Sugai, Takeshi
AU - Ohta, Hiromichi
PY - 1991/7
Y1 - 1991/7
N2 - The preparation of 4-hydroxy-β-ionone of high enantiomeric excess was achieved via lipase-catalyzed transesterification of the corresponding racemate as the key-step. Starting from Its (R)-enantiomer, (S)-6-hydroxy-α-ionone, an important intermediate for synthetic abscisic acid analogs, was synthesized.
AB - The preparation of 4-hydroxy-β-ionone of high enantiomeric excess was achieved via lipase-catalyzed transesterification of the corresponding racemate as the key-step. Starting from Its (R)-enantiomer, (S)-6-hydroxy-α-ionone, an important intermediate for synthetic abscisic acid analogs, was synthesized.
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U2 - 10.1080/00021369.1991.10870844
DO - 10.1080/00021369.1991.10870844
M3 - Article
AN - SCOPUS:0011478549
SN - 0916-8451
VL - 55
SP - 1873
EP - 1876
JO - Bioscience, Biotechnology and Biochemistry
JF - Bioscience, Biotechnology and Biochemistry
IS - 7
ER -