| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9565304 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
A new, general route to the benz[5,6]azepino[4,3-b]indole ring system has been developed via the 1,7-dipolar electrocyclisation reactions of azomethine ylides.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of benz[5,6]azepino[4,3-b]indoles by 1,7-electrocyclisation of azomethine ylides](/preview/png/9565304.png "First Page Preview: Synthesis of benz[5,6]azepino[4,3-b]indoles by 1,7-electrocyclisation of azomethine ylides")
Authors
Miklós Nyerges, Áron Pintér, Andrea Virányi, István Bitter, László TÅke,