Synthesis of 1-substituted 1-vinylcycloalkanes by allylboration of carbonyl compounds and ethoxyacetylene with diorganylborylethylidenecyclopentane and a diorganylborylethylidenecyclohexane
Preparation of 1-substituted 1-vinylcycloalkanes from 3,3-tetra- and 3,3-penta-methyleneallylboranes
作者:Yu.N. Bubnov、V.I. Zheludeva、A.V. Ignatenko
DOI:10.1016/0022-328x(89)85424-5
日期:1989.1
The boranes I and II, obtained by hydroboration of 1,1-tetra- and 1,1-pentamethyleneallenes with 9-BBN, were used as key reactants in the synthesis of a series of unsaturated gem-substituted carbinols (VIIa-VIIg, Xa-Xc, and XII), as well as 1,1-divinylcyclopentane and 1,1-divinylcyclohexane (XV and XVIII). The addition reactions of the boranes I and II to the carbonylcompounds and ethoxyacetylene