DFT Study of Stereoselective Ketene-imine Cycloadditions, Evaluation of Possible Solvent Effects with IEF-PCM

Abstract

The formal [2+2] cycloaddition of ketenes and imines, also known as Staudinger synthesis, is a facile method for the synthesis of biologically important β-lactam derivatives. In this paper two previously reported stereoselective reactions were investigated with computational methods. Our computations support experimental data that a chiral imine, derived from d-glyceraldehyde reacting with ketenes, yields almost exclusively one out of the possible four diastereomers. The reaction proceeds stepwise, first addition of the imine to the ketene yields an intermediate, then the product is formed in a conrotatory electrocyclization. Results indicate that the electrostatic repulsion of the chiral auxiliary group is the main factor of the stereoselectivity, but solvent and substituent effects are not negligible. Calculations were performed at M06-2X/6-31+G** level of theory combined with IEF-PCM solvation, in common solvents such as toluene, THF, dichloromethane, acetonitrile and water. These results provide useful insight for the development of new chiral auxiliaries and optimizing reaction parameters.

New bio-amphiphilic structures of sucrose via amides linkages

“…The solid separated by iltration, the iltrate washed, neutralized and dried by any available chemicals. The crude resulting after removal of the liquids was puri ied by on silica gel with 6:1 ethyl acetate-acetone to furnish the acetylated sucrose analogs as pure white crystals (Zavar et al, 2016;Komjáti et al, 2018;Ndugire et al, 2019;Deketelaere et al, 2017).…”