Please use this identifier to cite or link to this item:
https://idr.l2.nitk.ac.in/jspui/handle/123456789/13264
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Janardhanan, J.C. | - |
dc.contributor.author | James, K. | - |
dc.contributor.author | Puthuvakkal, A. | - |
dc.contributor.author | Bhaskaran, R.P. | - |
dc.contributor.author | Suresh, C.H. | - |
dc.contributor.author | Praveen, V.K. | - |
dc.contributor.author | Manoj, N. | - |
dc.contributor.author | Babu, B.P. | - |
dc.date.accessioned | 2020-03-31T08:45:29Z | - |
dc.date.available | 2020-03-31T08:45:29Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | New Journal of Chemistry, 2019, Vol.43, 25, pp.10166-10175 | en_US |
dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/13264 | - |
dc.description.abstract | A stoichiometry controlled domino cyclization reaction of hydrazone and p-benzoquinone to an angularly fused 3H-benzofuro[3,2-e]indazole core with an embedded oxygenated dibenzofuran framework under mild reaction conditions is disclosed. The reaction involves palladium catalyzed 5-hydroxy-1H-indazole formation followed by TFA mediated [3+2] annulation between the in situ formed 5-hydroxy-1H-indazole and p-benzoquinone. The developed method is attractive because of the concomitant formation of two heterocyclic rings with consecutive multiple bond forming events that include two C-C, one C-N and one C-O bonds. Spectroscopic and theoretical studies of the blue emissive benzofuroindazole derivatives have also been described. 2019 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. | en_US |
dc.title | Synthesis of hybrid polycycles containing fused hydroxy benzofuran and 1H-indazoles via a domino cyclization reaction | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
3 Synthesis of hybrid.pdf | 2.9 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.