2566-03-2Relevant articles and documents
ACYLATION OF CYCLOPROPYLACETYLENES WITH ACYLIUM FLUOROBORATES
Pomytkin, I. A.,Balenkova, E. S.,Anfilogova, S. N.
, p. 2027 - 2030 (2007/10/02)
The direction of acylation of cyclopropylacetylenes with acyl fluoroborates depends significantly on the character of substitution in the three-membered ring.In the case of 1,1-dichloro-2-methyl-2-ethynylcyclopropane the cyclopropane ring is opened, and fluoro ketones of the allene series are formed.During acylation of cyclopropylacetylene the three-membered ring rearranges to a four-membered ring with the formation of fluoro ketones of the cyclobutane series, and the rearrangement is stereospecific to a considerable degree.