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
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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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