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
Y1 - 1991
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 - 10.1271/bbb1961.55.1873
DO - 10.1271/bbb1961.55.1873
M3 - Article
AN - SCOPUS:85007676911
SN - 0002-1369
VL - 55
SP - 1873
EP - 1876
JO - Agricultural and biological chemistry
JF - Agricultural and biological chemistry
IS - 7
ER -