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Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes

[Image: see text] Gold(I) acetylide and σ,π-digold(I) alkyne complexes derived from one prototypical 1,6-enyne and from 7-ethynyl-1,3,5-cycloheptatriene have been prepared and structurally characterized. Their possible role in gold(I)-catalyzed cycloisomerizations has been studied by experiment and...

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Autores principales: Ferrer, Sofia, Echavarren, Antonio M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850095/
https://www.ncbi.nlm.nih.gov/pubmed/29551852
http://dx.doi.org/10.1021/acs.organomet.7b00668
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author Ferrer, Sofia
Echavarren, Antonio M.
author_facet Ferrer, Sofia
Echavarren, Antonio M.
author_sort Ferrer, Sofia
collection PubMed
description [Image: see text] Gold(I) acetylide and σ,π-digold(I) alkyne complexes derived from one prototypical 1,6-enyne and from 7-ethynyl-1,3,5-cycloheptatriene have been prepared and structurally characterized. Their possible role in gold(I)-catalyzed cycloisomerizations has been studied by experiment and by DFT calculations. Gold(I) acetylides are totally unproductive complexes in the absence of Brønsted acids. Similarly, no cyclizations were observed by heating σ,π-digold(I) alkyne digold(I) at least up to 130 °C. Theoretical studies provide a rationale for the much lower reactivity of digold species in reactions of enynes.
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spelling pubmed-58500952018-03-15 Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes Ferrer, Sofia Echavarren, Antonio M. Organometallics [Image: see text] Gold(I) acetylide and σ,π-digold(I) alkyne complexes derived from one prototypical 1,6-enyne and from 7-ethynyl-1,3,5-cycloheptatriene have been prepared and structurally characterized. Their possible role in gold(I)-catalyzed cycloisomerizations has been studied by experiment and by DFT calculations. Gold(I) acetylides are totally unproductive complexes in the absence of Brønsted acids. Similarly, no cyclizations were observed by heating σ,π-digold(I) alkyne digold(I) at least up to 130 °C. Theoretical studies provide a rationale for the much lower reactivity of digold species in reactions of enynes. American Chemical Society 2017-12-19 2018-03-12 /pmc/articles/PMC5850095/ /pubmed/29551852 http://dx.doi.org/10.1021/acs.organomet.7b00668 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Ferrer, Sofia
Echavarren, Antonio M.
Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title_full Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title_fullStr Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title_full_unstemmed Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title_short Role of σ,π-Digold(I) Alkyne Complexes in Reactions of Enynes
title_sort role of σ,π-digold(i) alkyne complexes in reactions of enynes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850095/
https://www.ncbi.nlm.nih.gov/pubmed/29551852
http://dx.doi.org/10.1021/acs.organomet.7b00668
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