Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/561
Title: | Palladium catalyzed reaction of ortho-functionalized aryl iodides with bicyclic hydrazines: facile route toward heteroannulated cyclopentenes and azabicycles |
Authors: | Jubi John Rani, R Sarath Chand, S Praveen, P Nayana Joseph Suresh, E Radhakrishnan, K V |
Keywords: | Azabicyclic alkene Aryl halide Palladium Heteroannulation Functionalized cyclopentene |
Issue Date: | 2013 |
Publisher: | Elsevier |
Citation: | Tetrahedron 69(1):152-159;7 Jan 2013 |
Abstract: | A palladium catalyzed tandem protocol for the synthesis of cyclopentene fused heterocycles from diazabicyclic alkenes and ortho-functionalized aryl iodides has been elaborated. This tandem protocol was utilized for the synthesis of a number of cyclopentene fused dihydrobenzofurans and indolines. The reaction can be tuned toward the formation of either 3,4-disubstituted cyclopentenes or cyclopentene fused heterocycles by careful manipulation of the reaction parameters. The reaction was also extended to bicyclic alkenes derived from fulvene, which resulted in the heteroannulation of the azabicyclic system |
URI: | http://hdl.handle.net/123456789/561 |
Appears in Collections: | 2013 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2013_0042.pdf Restricted Access | 1.13 MB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.