ELECTROPHILIC CARBOCYCLISATIONS, INCLUDING TANDEM PROCESSES, USING NOVEL COBALOXIME PI-CATION INTERMEDIATES

Citation
G. Kettschau et G. Pattenden, ELECTROPHILIC CARBOCYCLISATIONS, INCLUDING TANDEM PROCESSES, USING NOVEL COBALOXIME PI-CATION INTERMEDIATES, Synlett, (7), 1998, pp. 783-785
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
09365214
Issue
7
Year of publication
1998
Pages
783 - 785
Database
ISI
SICI code
0936-5214(1998):7<783:ECITPU>2.0.ZU;2-S
Abstract
Intramolecular cyclisations of substituted gamma- and delta-unsaturate d cobaloxime pi-cations (detived from 1 --> 4) are shown to occur from the 5-exo, 5-endo and 6-endo orientated double bonds but not from the corresponding 6-exo orientation, 2. An unprecedented tandem cyclisati on from the pyrrole substituted unsaturated hydroxy cobaloxime 19 in t he presence of pTSA leads to the tricycle 21 by way of the novel cobal t pi-cation intermediate 20.