STEREOCONTROLLED FUNCTIONALIZATION OF CYCLOOCTADIENE USING ORGANOIRONCHEMISTRY

Authors
PEARSON AJ BALASUBRAMANIAN S SRINIVASAN K
Citation
Aj. Pearson et al., STEREOCONTROLLED FUNCTIONALIZATION OF CYCLOOCTADIENE USING ORGANOIRONCHEMISTRY, Tetrahedron, 49(25), 1993, pp. 5663-5672
Citations number
30
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
49
Issue
25
Year of publication
1993
Pages
5663 - 5672
Database
ISI
SICI code
0040-4020(1993)49:25<5663:SFOCUO>2.0.ZU;2-D
Abstract
Methods are described for controlling the reactivity of cyclooctadieny liron cations so as to give good yields during the stereocontrolled ad dition of carbon nucleophiles, thereby leading to efficient functional ization of eight membered carbocycles.