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 |
推荐引用方式 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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