版权说明 操作指南
首页 > 成果 > 详情

Novozyme 435-Catalyzed Asymmetric Acylation of (R, S)-3-n-Butylphthalide in Hexane

认领
导出
Link by DOI
反馈
分享
QQ微信 微博
成果类型:
期刊论文
作者:
He, Laping*;Li, Cuiqin;Gao, Bing
通讯作者:
He, Laping
作者机构:
[He, Laping] Guizhou Univ, Key Lab Karst Environm & Geohazard Prevent, Minist Educ, Sch Chem Engn, Guiyang 550003, Guizhou Prov, Peoples R China.
[Gao, Bing] Wuhan Polytech Univ, Dept Biol & Pharmaceut Engn, Wuhan, Hubei Province, Peoples R China.
通讯机构:
[He, Laping] G
Guizhou Univ, Key Lab Karst Environm & Geohazard Prevent, Minist Educ, Sch Chem Engn, Guiyang 550003, Guizhou Prov, Peoples R China.
语种:
英文
关键词:
Asymmetric acylation;3-n-Butylphthalide;Molar ratio;Novozyme 435;Temperature;Water activity
期刊:
Preparative Biochemistry & Biotechnology
ISSN:
1082-6068
年:
2009
卷:
39
期:
3
页码:
266-276
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:
The asymmetric acylation of (R, S)-3-n-butylphthalide could be efficiently catalyzed by Novozyme 435. The effect of various reaction parameters such as water activity, temperature, molar ratio of acetic anhydride to (R, S)-3-nbutylphthalide, and reaction time on the asymmetric acylation were studied. The optimums of the reaction parameters were water activity 0.62, temperature 30°C, molar ratio of acetic anhydride to (R, S)-3-n-butylphthalide 8:1, and reaction time 48 h, respectively. Under the optimum conditions, enantiopure 3-n-butylphthalid...

反馈

验证码:
看不清楚,换一个
确定
取消

成果认领

标题:
用户 作者 通讯作者
请选择
请选择
确定
取消

提示

该栏目需要登录且有访问权限才可以访问

如果您有访问权限,请直接 登录访问

如果您没有访问权限,请联系管理员申请开通

管理员联系邮箱:yun@hnwdkj.com