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Rh-Catalyzed [3+2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids
Li, Yun[1,2]; Zhang, Qingyu[1]; Du, Qiucheng[1]; Zhai, Hongbin[1,3]
刊名ORGANIC LETTERS
2016
卷号18页码:4076-4079
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/2196351
专题华南理工大学
作者单位1.[1]Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
2.[2]Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
3.[3]Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Lab Chem Genom, Shenzhen 518055, Peoples R China
推荐引用方式
GB/T 7714
Li, Yun[1,2],Zhang, Qingyu[1],Du, Qiucheng[1],et al. Rh-Catalyzed [3+2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids[J]. ORGANIC LETTERS,2016,18:4076-4079.
APA Li, Yun[1,2],Zhang, Qingyu[1],Du, Qiucheng[1],&Zhai, Hongbin[1,3].(2016).Rh-Catalyzed [3+2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids.ORGANIC LETTERS,18,4076-4079.
MLA Li, Yun[1,2],et al."Rh-Catalyzed [3+2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids".ORGANIC LETTERS 18(2016):4076-4079.
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