α-Seleno arsonium ylides 5 have been synthesized through the reaetion of α- unfunctionalized arsonium ylides 4 with almost equimolar phenylselenenyl iodide 2.
a-Phenylthio-a, b-unsaturated esters 6 were synthesized by Witting reaction of 3, which were prepared by a phenylsulfenyllation-trans-ylidation reaction.
InCl34H2O catalyzes the cross-aldol condensation of cycloalkanones with aromatic aldehydes in sealed tube under solvent free condition to afford an efficient method for the synthesis of a, a-bis(substituted)benzyliden...InCl34H2O catalyzes the cross-aldol condensation of cycloalkanones with aromatic aldehydes in sealed tube under solvent free condition to afford an efficient method for the synthesis of a, a-bis(substituted)benzylidenecycloalkanones.展开更多
基金National Natural Science Foundation of China!29502006
文摘α-Seleno arsonium ylides 5 have been synthesized through the reaetion of α- unfunctionalized arsonium ylides 4 with almost equimolar phenylselenenyl iodide 2.
基金Project 29502006 was supported by the National Natural Science Foundation of China.
文摘a-Phenylthio-a, b-unsaturated esters 6 were synthesized by Witting reaction of 3, which were prepared by a phenylsulfenyllation-trans-ylidation reaction.
文摘InCl34H2O catalyzes the cross-aldol condensation of cycloalkanones with aromatic aldehydes in sealed tube under solvent free condition to afford an efficient method for the synthesis of a, a-bis(substituted)benzylidenecycloalkanones.