Enantioselective alkynylation of N-sulfonyl alpha-ketiminoesters via a Friedel-Crafts alkylation strategy | |
Liu, Ren-Rong[1]; Zhu, Lei[2]; Hu, Jiang-Ping[1]; Lu, Chuan-Jun[1]; Gao, Jian-Rong[1]; Lan, Yu[2]; Jia, Yi-Xia[1] | |
2017 | |
卷号 | 53页码:5890-5893 |
URL标识 | 查看原文 |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/3178502 |
专题 | 重庆大学 |
推荐引用方式 GB/T 7714 | Liu, Ren-Rong[1],Zhu, Lei[2],Hu, Jiang-Ping[1],et al. Enantioselective alkynylation of N-sulfonyl alpha-ketiminoesters via a Friedel-Crafts alkylation strategy[J],2017,53:5890-5893. |
APA | Liu, Ren-Rong[1].,Zhu, Lei[2].,Hu, Jiang-Ping[1].,Lu, Chuan-Jun[1].,Gao, Jian-Rong[1].,...&Jia, Yi-Xia[1].(2017).Enantioselective alkynylation of N-sulfonyl alpha-ketiminoesters via a Friedel-Crafts alkylation strategy.,53,5890-5893. |
MLA | Liu, Ren-Rong[1],et al."Enantioselective alkynylation of N-sulfonyl alpha-ketiminoesters via a Friedel-Crafts alkylation strategy".53(2017):5890-5893. |
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