Synthesis of oxepine-, oxocine- and azepine-annulated carbazole derivatives by combined Claisen rearrangement and diene/enyne metathesis

被引：31

作者：

Chattopadhyay, Shital K. ^{[1
]}

Roy, Shankar P. ^{[1
]}

Ghosh, Debalina ^{[1
]}

Biswas, Gautam ^{[1
]}

机构：

[1] Univ Kalyani, Dept Chem, Kalyani 741235, W Bengal, India

来源：

TETRAHEDRON LETTERS | 2006年 / 47卷 / 38期

关键词：

Claisen rearrangement; ring-closing metathesis; enyne metathesis; carbazole; oxepine; Diels-Alder reaction;

D O I：

10.1016/j.tetlet.2006.07.045

中图分类号：

O62 [有机化学];

学科分类号：

070303 [有机化学]; 081704 [应用化学];

摘要：

A new route to various medium ring heterocycle-annulated tetra-, penta- and hexacyclic carbazole derivatives has been developed using successive applications of three atom economic processes, viz. Claisen rearrangement, olefin metathesis and Diels-Alder reactions. (c) 2006 Elsevier Ltd. All rights reserved.

引用

页码：6895 / 6898

页数：4

共 39 条

[1]

[Anonymous], SCI SYNTHESIS

[2]

[Anonymous], 1987, PROG CHEM ORG NAT PR

[3]

Microwave-enhanced synthesis of N-shifted buflavine analogues via a Suzuki-ring-closing metathesis protocol [J].