Efficient access to alkynylated quinalizinones: Via the gold(i)-catalyzed aminoalkynylation of alkynes

35Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The gold-catalyzed aminoalkynylation of alkynes for the synthesis of quinalizinones is reported. For instance, the reaction of pyridinoalkynes with 1-[(triisopropylsilyl)-ethynyl]-1,2-benziodoxol-3(1H)-one (TIPS-EBX) in the presence of a catalytic amount of AuCl at 50 °C afforded alkynylated quinalizinones in 57-87% yields.

Cite

CITATION STYLE

APA

Shinde, P. S., Shaikh, A. C., & Patil, N. T. (2016). Efficient access to alkynylated quinalizinones: Via the gold(i)-catalyzed aminoalkynylation of alkynes. Chemical Communications, 52(52), 8152–8155. https://doi.org/10.1039/c6cc03414d

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