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J Org Chem ; 67(13): 4599-601, 2002 Jun 28.
Article in English | MEDLINE | ID: mdl-12076164

ABSTRACT

A practical synthesis of methyl (2R,3S)-3-(4-methoxyphenyl)glycidate (-)-2, a key intermediate for diltiazem (1), was developed. Treatment of methyl (E)-4-methoxycinnamate 3 with chiral dioxirane, generated from chiral ketone 4, provided (-)-2 in 77% ee and 89% yield. The crude mixture of (-)-2 and 4 was efficiently separated by the use of novel and simple equipment performing a lipase-catalyzed transesterification and a continuous dissolution and crystallization to furnish the optically pure (-)-2 and recovery of 4 in 74% and 91% yield, respectively.


Subject(s)
Diltiazem/chemistry , Epoxy Compounds/chemical synthesis , Propionates/chemical synthesis , Catalysis , Chemistry, Organic/instrumentation , Chemistry, Organic/methods , Chromatography, High Pressure Liquid , Cinnamates/chemistry , Epoxy Compounds/chemistry , Esterification , Lipase/metabolism , Magnetic Resonance Spectroscopy , Molecular Structure , Stereoisomerism
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