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Annellation of tricarbonylcyclobutadieneiron to the cycloheptatrienyl (tropylium) cation and to cyclohepta-2,4,6-trienone (tropone). Synthesis of some derivatives of (1,7,8,9-h-bicyclo[5,2,0]nonatetraene)tricarbonyliron.

Authors :
Stringer, MB
Wege, D
Source :
Australian Journal of Chemistry; 1978, Vol. 31 Issue: 7 p1607-1617, 11p
Publication Year :
1978

Abstract

The compounds (1,7,8,9-η-bicyclo[5,2,0]nonatetraenyl hexafluorophosphate)tricarbonyliron (9), (1,7,8,9-η-bicyclo[5,2,0]nona- 1(7),2,5,8-tetraen-4-one)tricarbonyliron (10), and (1,7,8,9-η-bicyclo- [5,2,0]nona-1(7),3,5,8-tetraen-2-one)tricarbonyliron (11) have been prepared. The cation (9) undergoes nucleophilic capture at C2, the position α to the coordinated cyclobutadiene ring. Oxidative removal of the tricarbonyliron group from the symmetrical tropone derivative (10) generates bicyclo-[5,2,0]nona-1(7),2,5,8-tetraen-4-one, which can be trapped as a Diels-Alder adduct with cyclopentadiene.

Details

Language :
English
ISSN :
00049425 and 14450038
Volume :
31
Issue :
7
Database :
Supplemental Index
Journal :
Australian Journal of Chemistry
Publication Type :
Periodical
Accession number :
ejs8408863
Full Text :
https://doi.org/10.1071/CH9781607