Annulation of 4-Hydroxypyrones and α-Keto Vinyl Azides; A Regiospecific Approach towards the Synthesis of Furo[3, 2-c]Pyrone Scaffolds under Catalyst Free Condition

11Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A mild and efficient strategy for the construction of furo[3, 2-c]pyrones via an annulation of α-keto vinyl azides and 4-hydroxypyrones under catalyst free condition has been described. Several furo[3, 2-c]pyrone scaffolds were synthesized from readily available vinyl azides and 4-hydroxypyrones in a regiospecific manner. This protocol allows the formation of new C−O and C−C bonds in a single step to provide a wide variety of substituted furano heterocycles. It is worth noting that the present protocol has several advantages over the conventional methods such as catalyst free, short reaction duration and operational simplicity with good yields.

Cite

CITATION STYLE

APA

Prasad, B., Reddy, V. G., Krishna, N. H., Reddy, N. V. S., Nanubolu, J. B., Alarifi, A., & Kamal, A. (2017). Annulation of 4-Hydroxypyrones and α-Keto Vinyl Azides; A Regiospecific Approach towards the Synthesis of Furo[3, 2-c]Pyrone Scaffolds under Catalyst Free Condition. ChemistrySelect, 2(26), 8122–8126. https://doi.org/10.1002/slct.201701980

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