Formation of a chiral 1-fluoro-2, 2-diphenylcyclopropyl radical in the Barton decarboxylation reaction
K Gawronska, J Gawronski…
Index: Gawronska, K.; Gawronski, J.; Walborsky, H. M. Journal of Organic Chemistry, 1991 , vol. 56, # 6 p. 2193 - 2197
Full Text: HTML
Citation Number: 24
Abstract
The thermal decomposition of N-hydroxypyridine-2-thione esters to produce radicals which can react with a variety of halogen-donating reagents resulting in an halogenative decarboxylation reaction or with H-atom donating sources to give rise to products of decarboxylation has been given the appellation, Barton decarboxylation reaction. 2 In an ancillary study the need arose to prepare chiral l-bromo-l-fluoro-2, 2- ...
Related Articles:
Fluorination with xenon difluoride. Reaction with phenylsubstituted olefins
[Zupan,M.; Pollak,A. Journal of Organic Chemistry, 1976 , vol. 41, # 25 p. 4002 - 4004]