Premium
Copper(I)‐Catalyzed Three‐Component Reaction of Terminal Propargyl Alcohols, Aldehydes, and Amines: Synthesis of 3‐Amino‐2‐pyrones and 2,5‐Dihydrofurans
Author(s) -
Fan Wu,
Ma Shengming
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201408826
Subject(s) - propargyl , chemistry , isomerization , aldehyde , allene , furan , catalysis , amine gas treating , alkyne , component (thermodynamics) , intramolecular force , organic chemistry , ring (chemistry) , medicinal chemistry , physics , thermodynamics
Abstract A novel copper(I)‐catalyzed three‐component reaction for the efficient synthesis of 3‐amino‐2‐pyrones and 2,5‐dihydrofurans from propargyl alcohols, aldehydes, and amines has been developed. The starting materials are easily available and the scope of this method is broad. Through mechanistic studies, it is believed that the three‐component reaction consists of an A 3 ‐coupling to propargylic amine, alkyne–allene isomerization, and intramolecular cyclization of the allenol to form a furan. In case of using ethyl glyoxalate as the aldehyde, a ring‐opening, lactonization, and isomerization process affords the 3‐amino‐2‐pyrones.