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Regioselective Synthesis of 2‐Acylquinazolines and 3H‐1,4‐Benzodiazepin‐3‐ones by a Ugi 4CC/Staudinger/aza‐Wittig Sequence

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成果类型:
期刊论文
作者:
Zhong, Ying;Zhang, Hao;Ding, Ming-Wu*
通讯作者:
Ding, Ming-Wu
作者机构:
[Zhong, Ying; Ding, Ming-Wu; Zhang, Hao] Cent China Normal Univ, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
[Zhong, Ying] Southwest Univ Nationalities, Coll Chem & Environm Protect Engn, Chengdu 610041, 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
期刊:
Journal of Heterocyclic Chemistry
ISSN:
0022-152X
年:
2015
卷:
52
期:
2
页码:
330-335
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21172085]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
α-Acylamino-carboxamide azides 1, obtained from Ugi reactions of o-azidobenzaldehyde, amines, benzoylformic acid, and isocyanides, reacted with triphenylphosphine to give various 2-acylquinazolines 3 and/or 3H-1,4-benzodiazepin-3-ones 4 in moderate to good yields via sequential Staudinger and intramolecular aza-Wit...

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