Switchable Selectivity in the Annulation of o‐Trifluoroacetylanilines and Activated Terminal Alkynes Based on Transition Metal and Phosphine Catalysis

Author:

Mitrofanov Alexander Yu.1ORCID,Murashkina Arina V.1,Lyssenko Konstantin A.12,Beletskaya Irina P.1

Affiliation:

1. Department of Chemistry Lomonosov Moscow State University Leninskie Gory, GSP-1 Moscow 119991 Russian Federation

2. G.V. Plekhanov Russian University of Economics 36 Stremyanny Per. Moscow 117997 Russian Federation

Abstract

AbstractIn this work, we have developed selective methods for the synthesis of quinoline‐2‐carboxylates and quinoline‐3‐carboxylates as well as (indolin‐2‐ylidene)acetates through copper‐, silver‐, or phosphine‐catalyzed reaction of propiolates with 2′‐amino‐2,2,2‐trifluoroacetophenones. The approaches proposed ensure synthesis of substituted quinoline carboxylates and (indolin‐2‐ylidene)acetates in good yields. Introduction of alkynones into the reaction with 2′‐amino‐2,2,2‐trifluoroacetophenones gives acyl substituted derivatives in good yields.

Funder

Russian Science Support Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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