DSpace Repository

Palladium catalyzed reaction of ortho-functionalized aryl iodides with bicyclic hydrazines: facile route toward heteroannulated cyclopentenes and azabicycles

Show simple item record

dc.contributor.author Jubi John
dc.contributor.author Rani, R
dc.contributor.author Sarath Chand, S
dc.contributor.author Praveen, P
dc.contributor.author Nayana Joseph
dc.contributor.author Suresh, E
dc.contributor.author Radhakrishnan, K V
dc.date.accessioned 2013-07-17T08:54:35Z
dc.date.available 2013-07-17T08:54:35Z
dc.date.issued 2013
dc.identifier.citation Tetrahedron 69(1):152-159;7 Jan 2013 en_US
dc.identifier.uri http://hdl.handle.net/123456789/561
dc.description.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 en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Azabicyclic alkene en_US
dc.subject Aryl halide en_US
dc.subject Palladium en_US
dc.subject Heteroannulation en_US
dc.subject Functionalized cyclopentene en_US
dc.title Palladium catalyzed reaction of ortho-functionalized aryl iodides with bicyclic hydrazines: facile route toward heteroannulated cyclopentenes and azabicycles en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

  • 2013
    2013 publications

Show simple item record

Search DSpace


Advanced Search

Browse

My Account