Diastereoselective epoxidation of alpha’-alkoxy substttuted cyclohexenyl ketones
摘要:
The stereochemistry of nucleophilic epoxidation of alpha,beta-unsaturated-alpha-alkoxy substituted ketones with t-butylhydroperoxide in the presence of Triton B is determined by the alpha'-alkoxy substituent via a Felkin-Ahn type transition state.
Diastereoselective epoxidation of alpha’-alkoxy substttuted cyclohexenyl ketones
摘要:
The stereochemistry of nucleophilic epoxidation of alpha,beta-unsaturated-alpha-alkoxy substituted ketones with t-butylhydroperoxide in the presence of Triton B is determined by the alpha'-alkoxy substituent via a Felkin-Ahn type transition state.