Cyclization of ethyl diallylacetate or ethyl diallylmalonate to cyclopentane derivatives during the addition of perfluoroalkyl and trichloromethyl radicals
NO Brace
Index: Brace,N.O. Journal of Organic Chemistry, 1969 , vol. 34, p. 2441 - 2445
Full Text: HTML
Citation Number: 11
Abstract
XIV, Y= H XV, Y= COOCzH, analysis. Little if any VI or XV was present in reaction products. One reason for the small amount of V observed in reaction product mixtures was that cyclization to a y-lactone occurred during attempted isolation. I3 A sample of XVI was trapped from glpc separa-f [CJ+ sII-q--J
Related Articles:
Synthesis and supramolecular properties of conformationally restricted and flexible phospholipids
[Vares, Lauri; Koulov, Atanas V.; Smith, Bradley D. Journal of Organic Chemistry, 2003 , vol. 68, # 26 p. 10073 - 10078]
A new synthesis of 2, 10, 11-trioxatricyclo [4.4. 4.01, 6] tetradecane
[Beaulieu, Normand; Deslongchamps, Pierre Canadian Journal of Chemistry, 1980 , vol. 58, p. 875 - 877]
A flexible Pinner preparation of orthoesters: the model case of trimethylorthobenzoate
[McElvain; Kundiger Journal of the American Chemical Society, 1942 , vol. 64, p. 254,259]