I2/CHP mediated [1+1+1+1] cyclization of aromatic isocyanides with amines to construct 1,3-diazetidine-2,4-diimine derivatives

被引：4
作者：
Liu, Hai-Feng [1 ,2 ,3 ]
Zhu, Tong-Hao [1 ,2 ]
Xu, Pei [1 ,2 ]
Wang, Shun-Yi [1 ,2 ]
Ji, Shun-Jun [1 ,2 ]
机构：
[1] Soochow Univ, Key Lab Organ Synth Jiangsu Prov, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215123, Peoples R China
[3] WISPO Adv Mat SuZhou Co Ltd, Room D 904,338 Ruoshui St,Suzhou Ind Pk, Suzhou 215123, Peoples R China
来源：
ORGANIC & BIOMOLECULAR CHEMISTRY | 2017年 / 15卷 / 41期
基金：
中国国家自然科学基金;
关键词：
METAL-CATALYZED REACTIONS; RAY MOLECULAR-STRUCTURE; TERT-BUTYL ISOCYANIDE; PHENANTHRIDINE DERIVATIVES; EFFICIENT SYNTHESIS; ALPHA-ISOCYANOACETAMIDES; MULTICOMPONENT REACTIONS; OXIDATIVE ANNULATION; DIVERGENT SYNTHESIS; BUILDING-BLOCKS;
D O I：
10.1039/c7ob02255g
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An I-2/CHP (cumene hydroperoxide) mediated [1 + 1 + 1 + 1] cyclization of aromatic isocyanides with readily accessible amines via the formation 4 new C-N bonds has been developed to construct unsymmetric 1,3-diazetidine-2,4-diimine derivatives under mild conditions.
引用
收藏
页码：8738 / 8742
页数：5
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