Solid state photolysis of inclusionmolecularcomplexes of N,N-dialkylpyruvamides with deoxycholicacid or cyclodextrin gave the corresponding β-lactams as main products. The chemo-, stereo- and regioselectivities of the solid state reactions were different from those of the reactions in solution. Asymmetric induction due to the chirality of deoxycholicacid or cyclodextrin was observed.
Photochemical reaction of inclusion molecular complexes of N,N-dialkylpyruvamides with desoxycholic acid. Host-controlled reaction of guest compounds in the solid state
Solidstate photolysis of inclusion molecular complexes of N,N-dialkylpyruvamides with desoxycholic acid gives the corresponding β-lactams which are not obtained in the corresponding photoreaction of the pyruvamides in solution.