Fluorocyclopropanes. I. Preparation and nuclear magnetic resonance spectra
PB Sargeant
Index: Sargeant,P.B. Journal of Organic Chemistry, 1970 , vol. 35, p. 678 - 682
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Citation Number: 72
Abstract
Hexafluoropropylene epoxide transfers a difluoromethylene group to olefins in a general and convenient synthesis of fluorinated cyclopropanes. However, loss of stereospecificity can result from thermal isomerization of the fluorinated cyclopropane, which occurs slowly near 200". The nmr spectra of the fluorinated cyclopropanes show that generally the vicinal coupling constants cis JEF (9-17 Hz) and cis JFF (5-10 Hz) are greater than trans JHF (1-2 ...
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