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Iodine promoted cascade cycloisomerization of 1-en-6,11-diynes.

Authors :
Qiu, Yi-Feng
Niu, Yue-Jie
Song, Xian-Rong
Wei, Xi
Chen, Hui
Li, Shun-Xi
Wang, Xi-Cun
Huo, Congde
Quan, Zheng-Jun
Liang, Yong-Min
Source :
Chemical Communications. 1/28/2020, Vol. 56 Issue 9, p1421-1424. 4p.
Publication Year :
2020

Abstract

An iodine promoted cascade cycloisomerization of 1-en-6,11-diynes is presented for the easy preparation of tetrahydrobenzo[f]isoquinolines. This developed reaction system is identified as having good functional-group applicability and can be scaled up to gram quantities. In this transformation, two new cyclic frameworks and one carbonyl group are formed with four new bonds constructed. Additionally, the resulting iodo-substituted compounds could be further derived through simple elimination reactions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13597345
Volume :
56
Issue :
9
Database :
Academic Search Index
Journal :
Chemical Communications
Publication Type :
Academic Journal
Accession number :
141452364
Full Text :
https://doi.org/10.1039/c9cc08286g