A straightforward approach to robust thiazolylidene gold complexes: efficient catalysts for propargylamide cycloisomerizations

The straightforward synthesis of new thiazolylidene gold complexes is described. Despite their decreased steric protection, these complexes demonstrate excellent stability and high catalytic activity in the HFIP-assisted cycloisomerization of propargylamides. The synthesis and catalytic activity of a novel, stable thiazolylidene gold alkoxide complex is also reported.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt02258d
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

A straightforward approach to robust thiazolylidene gold complexes: efficient catalysts for propargylamide cycloisomerizations

Savvas G. Chalkidis, Georgios C. Vougioukalakis, Nikolaos Tsoureas, Steven P. Nolan
1 citations
Dalton Transactions
Catalytic Alkyne Reactions
0.94
article

A straightforward approach to robust thiazolylidene gold complexes: efficient catalysts for propargylamide cycloisomerizations

Savvas G. Chalkidis, Georgios C. Vougioukalakis, Nikolaos Tsoureas, Steven P. Nolan
article en
1 citations

Abstract

The straightforward synthesis of new thiazolylidene gold complexes is described. Despite their decreased steric protection, these complexes demonstrate excellent stability and high catalytic activity in the HFIP-assisted cycloisomerization of propargylamides. The synthesis and catalytic activity of a novel, stable thiazolylidene gold alkoxide complex is also reported.

Dalton TransactionsVol. 54(39)
National and Kapodistrian University of Athens (GR), Ghent University (BE)
Openalex Percentile: Top 21%
Catalytic Alkyne Reactions
0.94
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