56421-06-8Relevant articles and documents
Diastereoselectivity in the epoxidation of substituted cyclohexenes by dimethyldioxirane
Murray, Robert W.,Singh, Megh,Williams, Brian L.,Moncrieff, Hazel M.
, p. 1830 - 1841 (2007/10/03)
Three series of compounds based on the cyclohexene framework have been epoxidized by dimetbyldioxirane. A pronounced dependence of epoxide diastereoselectivity on substituent has been observed. In addition there is a solvent influence on this stereoselectivity. The results have been explained by invoking steric, H-bonding, and dipole - dipole influences on the epoxide stereochemistry.
Syn Bromination of 2-Cyclohexen-1-ol Benzoates. Isolation of a trans-3-Bromocyclohexano-cis-1,2-(2'-anisyl-1',3'-dioxolan-2'-ylium) Intermediate
Bellucci, Giuseppe,Bianchini, Roberto,Vecchiani, Sandra
, p. 3355 - 3362 (2007/10/02)
The addition of molecular bromine to 2-cyclohexen-1-ol benzoate, p-methylbenzoate, and p-methoxybenzoate in aprotic solvents of low to moderate dielectric constant gave, besides the expected vicinal trans diaxial and diequatorial dibromides, large amounts