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Stereoselective synthesis of the tricyclic core ABC-rings of nakadomarin and manzamine from a common intermediate

Authors :
Magnus, Philip
Fielding, Mark R.
Wells, Charles
Lynch, Vince
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Feb2002, Vol. 43 Issue 6, p947. 4p.
Publication Year :
2002

Abstract

Pauson–Khand cyclization of the enamide 9 proceeds in trifluoroethanol to give cyclopentenone 10, which on hydrogenation gives 11, having the core ABC-rings of nakadomarin 1. [Copyright &y& Elsevier]

Subjects

Subjects :
*ORGANIC synthesis
*HYDROGENATION

Details

Language :
English
ISSN :
00404039
Volume :
43
Issue :
6
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 :
7746587
Full Text :
https://doi.org/10.1016/S0040-4039(01)02301-2