4104-56-7Relevant 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.
SUBSTITUTION REACTIONS WITH PARTICIPATION OF ORGANOALUMINIUM COMPOUNDS 3. CROSS-COMBINATION OF ALLYL ACETATES WITH TRIALKYLALANES
Tolstikov, G. A.,Spivak, A. Yu.,Kuchin, A. V.,Lomakina, S. I.
, p. 1035 - 1040 (2007/10/02)
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