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One-pot synthesis of 5-oxopyrrolidine-2-carboxamides via a tandem Ugi 4CC/SN cyclization starting from Baylis–Hillman bromides

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成果类型:
期刊论文
作者:
Zeng, Xiao-Hua;Wang, Hong-Mei;Wu, Lei;Ding, Ming-Wu*
通讯作者:
Ding, Ming-Wu
作者机构:
[Zeng, Xiao-Hua; Ding, Ming-Wu; Wu, Lei] Cent China Normal Univ, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
[Zeng, Xiao-Hua; Wang, Hong-Mei] Hubei Univ Med, Inst Med Chem, Shiyan 442000, Peoples R China.
通讯机构:
[Ding, Ming-Wu] C
Cent China Normal Univ, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
语种:
英文
关键词:
pyrrole derivatives;ring closure reactions;multicomponent reactions
期刊:
Tetrahedron
ISSN:
0040-4020
年:
2013
卷:
69
期:
19
页码:
3823-3828
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21172085, 21032001]; Shiyan Municipal Science and Technology Bureau [ZD2011029]
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 one-pot base-mediated synthesis of 5-oxopyrrolidine-2-carboxamides was developed. The reaction of Baylis–Hillman bromides 1, primary amines 2, isocyanides 3 and arylglyoxals 4 produced the 5-oxopyrrolidine-2-carboxamides 6 in good yields via a tandem Ugi condensation and intramolecular substitution at room...

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