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Stereoselective synthesis of the tricyclic core ABC-rings of nakadomarin and manzamine from a common intermediate
- 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 :
- *ORGANIC synthesis
*HYDROGENATION
Subjects
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