TANDEM RING EXPANSION-CYCLIZATION REACTIONS - SYNTHESIS OF THE BICYCLO-[4.3.0]-NONANE AND BICYCLO-[6.3.0]-UNDECANE RING-SYSTEMS

Citation
Ki. Bookermilburn et Df. Thompson, TANDEM RING EXPANSION-CYCLIZATION REACTIONS - SYNTHESIS OF THE BICYCLO-[4.3.0]-NONANE AND BICYCLO-[6.3.0]-UNDECANE RING-SYSTEMS, Synlett, (8), 1993, pp. 592-594
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
09365214
Issue
8
Year of publication
1993
Pages
592 - 594
Database
ISI
SICI code
0936-5214(1993):8<592:TRER-S>2.0.ZU;2-O
Abstract
Ferric chloride induced ring expansion-cyclisation of cyclopropyl sily l ether derivitives provided access to functionalised [4.3.0] and [6.3 .0] carbocycles.