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	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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