Intramolecular cyclization of: N-allyl propiolamides: A facile synthetic route to highly substituted γ-lactams (a review)

43Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

Abstract

The development of simple and efficient methods for construction of substituted γ-lactams is an important synthetic goal because such ring skeletons are present in numerous natural compounds that display diverse biological activities. Intramolecular cyclization of N-allyl propiolamides is an efficient, economic, and operationally simple strategy for the synthesis of the titled compounds. In the present review we will discuss recent advances in the synthesis of functionalized γ-lactam derivatives from these easily accessible and versatile building blocks with the emphasis on the mechanistic aspects of the reactions.

Cite

CITATION STYLE

APA

Soleimani-Amiri, S., Vessally, E., Babazadeh, M., Hosseinian, A., & Edjlali, L. (2017). Intramolecular cyclization of: N-allyl propiolamides: A facile synthetic route to highly substituted γ-lactams (a review). RSC Advances. Royal Society of Chemistry. https://doi.org/10.1039/c7ra03075d

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free