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One-pot regioselective synthesis of β-lactams by a tandem Ugi 4CC/SN cyclization

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成果类型:
期刊论文
作者:
Zeng, Xiao-Hua;Wang, Hong-Mei;Yan, Yan-Mei;Wu, Lei;Ding, Ming-Wu*
通讯作者:
Ding, Ming-Wu
作者机构:
[Zeng, Xiao-Hua; Wang, Hong-Mei; Yan, Yan-Mei; Ding, Ming-Wu; Wu, Lei] Cent China Normal Univ, Key Lab Pesticide & Chem Biol, Minist Educ, 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, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China.
语种:
英文
关键词:
FNXAMJPEFLDGRO-UHFFFAOYSA-N;GRSJPBHIVBURKC-UHFFFAOYSA-N;InChIKeys;OGSUJCYWRMGORD-UHFFFAOYSA-N;QRCXOJMNYQXOTQ-UHFFFAOYSA-N
期刊:
Tetrahedron
ISSN:
0040-4020
年:
2014
卷:
70
期:
23
页码:
3647-3652
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21172085, 21032001]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
beta-Lactam scaffold was fabricated regioselectively by a facile one-pot base-mediated synthesis. The reactions of bromoacetic acid 1, primary amines 2, isocyanides 3, and arylglyoxals 4 produced 2-aroyl-4-oxoazetidine-2-carboxamides 6 in good yields via a one-pot tandem Ugi condensation and intramolecular C-alkylation at room temperature in the presence of C...

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