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AN EFFICIENT SYSTEM FOR THE ASYMMETRIC ACYLATION OF (R,S)-3-n-BUTYLPHTHALIDE CATALYZED BY NOVOZYME 435

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成果类型:
期刊论文
作者:
Li, Cuiqin*;He, Laping;Qiu, Baoquan;Gao, Bing
通讯作者:
Li, Cuiqin
作者机构:
[Li, Cuiqin; He, Laping] Guizhou Univ, Sch Mingde, Guiyang 550004, Guizhou Prov, Peoples R China.
[Li, Cuiqin] Guizhou Univ, Sch Chem Engn, Guiyang 550004, Guizhou Prov, Peoples R China.
[Qiu, Baoquan] Guangshui 1 Senior High Sch, Guangshui, Hubei Prov, Peoples R China.
[Gao, Bing] Wuhan Polytech Univ, Dept Biol & Pharmaceut Engn, Wuhan, Hubei Prov, Peoples R China.
通讯机构:
[Li, Cuiqin] G
Guizhou Univ, Sch Mingde, Guiyang 550004, Guizhou Prov, Peoples R China.
语种:
英文
关键词:
asymmetric acylation;3-n-butylphthalide;mixed media;Novozyme 435;tetrahydrofuran content;water content
期刊:
Preparative Biochemistry & Biotechnology
ISSN:
1082-6068
年:
2010
卷:
40
期:
4
页码:
354-365
基金类别:
Guizhou Science and Technology Fund [(2009) 2283]; Guizhou University [(2009) 022]
机构署名:
本校为其他机构
院系归属:
生命科学与技术学院
摘要:
Novozyme 435 could be a highly efficient catalyst in the asymmetric acylation of (R,S)-3-n-butylphthalide in tetrahydrofuran-hexane solvents. The effect of various reaction parameters such as agitation velocity, water content, mixed media, temperature, concentration of Novozyme 435, molar ratio of acetic anhydride to (R,S)-3-n-butylphthalide, reaction time, enantiomeric excess of substrate (eeS), enantiomeric excess of product (eeP), and enantioselective ratio (E) were studied. Tetrahydrofuran markedly improved (R,S)-3-n- butylphthalide convers...

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