SYNTHESIS OF NOVEL C-4 DISUBSTITUTED β-LACTAMS THROUGH STAUDINGER CYCLOADDITION REACTION

Authors

Robert Rodriguez, The University of Texas Rio Grande Valley
Anjali Nambiar, The University of Texas Rio Grande Valley
Ram N. Yadav, The University of Texas Rio Grande Valley
Bimal K. Banik, The University of Texas Rio Grande ValleyFollow

Document Type

Article

Publication Date

2014

Abstract

Synthesis of novel C-4 disubstituted beta-lactam that has N-methyl pyrrole system has been achieved through Staudinger cycloaddition reaction of acid chloride and imine. Interestingly, this reaction has produced a single stereoisomer.

Comments

© 2014 Heterocyclic Letters. Original published version available at http://www.heteroletters.org/issue43/PDF/Paper-14.pdf

Recommended Citation

Rodriguez, R., Nambiar, A., Yadav, R., & Banik, B. (2014). SYNTHESIS OF NOVEL C-4 DISUBSTITUTED β-LACTAMS THROUGH STAUDINGER CYCLOADDITION REACTION. Heterocyclic Letters, 4(3), 417–419.

First Page

417

Last Page

419

Publication Title

Heterocyclic Letters