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Reductive Heck coupling: an efficient approach toward the iboga alkaloids. Synthesis of ibogamine, epiibogamine and iboga analogs

Authors :
Jana, Goutam Kumar
Sinha, Surajit
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Mar2012, Vol. 53 Issue 13, p1671-1674. 4p.
Publication Year :
2012

Abstract

Abstract: A mild and efficient synthetic route to the iboga scaffold by employing reductive-Heck type annulation is described. The utility of this process is demonstrated by the direct access to the ibogamine, epiibogamine and iboga-analogs. The cyclization precursors were readily obtained from 2-iodoaniline by heteroannulation reaction with suitable alkynes followed by iodination. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
53
Issue :
13
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
71896398
Full Text :
https://doi.org/10.1016/j.tetlet.2012.01.097