中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Organocatalytic asymmetric Michael reaction with acylsilane donors

文献类型:期刊论文

作者Wu, Lei ; Li, Guangxun ; Fu, Qingquan ; Yu, Luoting ; Tang, Zhuo
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期2013
卷号11期号:3页码:443-447
ISSN号1477-0520
产权排序1
通讯作者Yu, LT (reprint author), Sichuan Univ, W China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China ; Tang, Zhuo
英文摘要We have developed an organocatalytic asymmetric Michael reaction of acylsilane through the selection of acylsilane substrates and organocatalysts, thus creating a rare example of acylsilane alpha-alkylation with a chiral guanidine catalyst, which afforded products in good yields and high stereoselectivity. The corresponding adducts described here have also been demonstrated to be useful in the synthesis of unnatural amino acids and biologically active compounds.
学科主题Chemistry
收录类别SCI
语种英语
WOS记录号WOS:000312217700009
公开日期2014-11-21
源URL[http://210.75.237.14/handle/351003/24191]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Wu, Lei,Li, Guangxun,Fu, Qingquan,et al. Organocatalytic asymmetric Michael reaction with acylsilane donors[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2013,11(3):443-447.
APA Wu, Lei,Li, Guangxun,Fu, Qingquan,Yu, Luoting,&Tang, Zhuo.(2013).Organocatalytic asymmetric Michael reaction with acylsilane donors.ORGANIC & BIOMOLECULAR CHEMISTRY,11(3),443-447.
MLA Wu, Lei,et al."Organocatalytic asymmetric Michael reaction with acylsilane donors".ORGANIC & BIOMOLECULAR CHEMISTRY 11.3(2013):443-447.

入库方式: OAI收割

来源:成都生物研究所

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