Synthesis, Separation and Absolute Configuration Determination by ECD Spectroscopy and TDDFT Calculations of 3-Amino-β-lactams and Derived Guanidines

July 28, 2017

Title

Synthesis, Separation and Absolute Configuration Determination by ECD Spectroscopy and TDDFT Calculations of 3-Amino-β-lactams and Derived Guanidines

Author

Tonko Dražić, Marin Roje, Mladenka Jurin, Gennaro Pescitelli

Year

2016

Journal

European Journal of Organic Chemistry

Abstract

Four isomeric chiral 3-amino-β-lactams 4 with p-fluorophenyl and p-methoxyphenyl substituents at N and C-4 positions, similar to the cholesterol absorption inhibitor ezetimibe, have been prepared as diastereomerically and enantiomerically pure compounds by ester enolate/imine cyclocondensation. The same route afforded analogues with a 1,3-benzodioxole instead of the p-methoxyphenyl group. Moreover, β-lactams 4a,b were converted into benzoylguanidine derivatives. The series of chiral β-lactams and β-lactam guanidines was characterized by electronic circular dichroism (ECD) spectroscopy, and their absolute configurations were assigned based on ECD TDDFT calculations. The calculations also demonstrated that the β-lactam sector and helicity rules cannot be applied to β-lactams appended with aromatic chromophores such as the present ezetimibe analogues.

Instrument

J-715

Keywords

Circular dichroism, Absolute configuration, Medicinal