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Enantioselective synthesis of beta-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative
He Ming; Pan ZhaoXi; Bai Song; Li Pei; Zhang YuPing; Jin LinHong; Hu DeYu; Yang Song; Song BaoAn
2013
卷号56期号:3页码:321-328
URL标识查看原文
WOS记录号WOS:000314890600009
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/5756586
专题贵州大学
作者单位[1]Guizhou Univ, State Key Lab Breeding Base Green Pesticides & Ag, Key Lab Green Pesticides & Agr Bioengn, Minist Educ, Guiyang 550025, Peoples R China
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GB/T 7714
He Ming,Pan ZhaoXi,Bai Song,et al. Enantioselective synthesis of beta-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative[J],2013,56(3):321-328.
APA He Ming.,Pan ZhaoXi.,Bai Song.,Li Pei.,Zhang YuPing.,...&Song BaoAn.(2013).Enantioselective synthesis of beta-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative.,56(3),321-328.
MLA He Ming,et al."Enantioselective synthesis of beta-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative".56.3(2013):321-328.
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