Highly regio- and diastereoselective (3+3)-cycloannulation of carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis

A highly regio- and diastereoselective (3+3)-cycloannulation of <i>in situ</i> generated carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis is reported. This work is the first to describe a silver catalysed synthesis of 3,4-fused furan with an oxa-bridged motif. The scope of the reaction is broad and the oxa-bridged furan products were obtained in good to high yields and with excellent regio- and diastereoselectivities.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02003d
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87
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article

Highly regio- and diastereoselective (3+3)-cycloannulation of carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis

Subhas Chandra Pan, Jharna Barman
2 citations
Chemical Communications
Cyclopropane Reaction Mechanisms
1.87
article

Highly regio- and diastereoselective (3+3)-cycloannulation of carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis

Subhas Chandra Pan, Jharna Barman
article en
2 citations

Abstract

A highly regio- and diastereoselective (3+3)-cycloannulation of <i>in situ</i> generated carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis is reported. This work is the first to describe a silver catalysed synthesis of 3,4-fused furan with an oxa-bridged motif. The scope of the reaction is broad and the oxa-bridged furan products were obtained in good to high yields and with excellent regio- and diastereoselectivities.

Chemical CommunicationsVol. 61(50)
Indian Institute of Technology Guwahati (IN)
Openalex Percentile: Top 16%
Cyclopropane Reaction Mechanisms
1.87
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