C6' steric bulk of cinchona alkaloid enables an enantioselective Michael addition/annulation sequence toward pyranopyrazoles. | |
Bao, Xiaoze; Wei, Shiqiang; Qu, Jingping; Wang, Baomin | |
刊名 | Chemical communications (Cambridge, England) |
2018 | |
卷号 | 54页码:2028-2031 |
ISSN号 | 1364-548X |
URL标识 | 查看原文 |
WOS记录号 | [DB:DC_IDENTIFIER_WOSID] |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/3272541 |
专题 | 大连理工大学 |
作者单位 | Dalian Univ Technol, Sch Pharmaceut Sci & Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China. |
推荐引用方式 GB/T 7714 | Bao, Xiaoze,Wei, Shiqiang,Qu, Jingping,et al. C6' steric bulk of cinchona alkaloid enables an enantioselective Michael addition/annulation sequence toward pyranopyrazoles.[J]. Chemical communications (Cambridge, England),2018,54:2028-2031. |
APA | Bao, Xiaoze,Wei, Shiqiang,Qu, Jingping,&Wang, Baomin.(2018).C6' steric bulk of cinchona alkaloid enables an enantioselective Michael addition/annulation sequence toward pyranopyrazoles..Chemical communications (Cambridge, England),54,2028-2031. |
MLA | Bao, Xiaoze,et al."C6' steric bulk of cinchona alkaloid enables an enantioselective Michael addition/annulation sequence toward pyranopyrazoles.".Chemical communications (Cambridge, England) 54(2018):2028-2031. |
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