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Multicomponent Coupling Cyclization Access to Cinnolines via in Situ Generated Diazene with Arynes, and α‑Bromo Ketones

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成果类型:
期刊论文
作者:
Shu, Wen-Ming;Ma, Jun-Rui;Zheng, Kai-Lu;Wu, An-Xin*吴安心
通讯作者:
Wu, An-Xin(吴安心
作者机构:
[Wu, An-Xin; Ma, Jun-Rui; Zheng, Kai-Lu; Shu, Wen-Ming] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China.
通讯机构:
[Wu, An-Xin] C
Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China.
语种:
英文
期刊:
Organic Letters
ISSN:
1523-7060
年:
2016
卷:
18
期:
2
页码:
196-199
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21272085, 21472056]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
A transition-metal-free multicomponent coupling cyclization reaction was explored involving arynes, tosylhydrazine, and α-bromo ketones. The reaction proceeds via a formal [2 + 2 + 2] cycloaddition, giving access to cinnoline derivatives in moderate yields under mild conditions. Three chemical bonds were formed-two C-N bonds and one C-C bond-in a single ...

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