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Construction of cyclic enones via gold-catalyzed oxygen transfer reactions

During the last decade, gold-catalyzed reactions have become a tour de force in organic synthesis. Recently, the gold-, Brønsted acid- or Lewis acid-catalyzed oxygen transfer from carbonyl to carbon–carbon triple bond, the so-called alkyne–carbonyl metathesis, has attracted much attention because th...

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Detalles Bibliográficos
Autores principales: Liu, Leping, Xu, Bo, Hammond, Gerald B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107534/
https://www.ncbi.nlm.nih.gov/pubmed/21647265
http://dx.doi.org/10.3762/bjoc.7.71
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author Liu, Leping
Xu, Bo
Hammond, Gerald B
author_facet Liu, Leping
Xu, Bo
Hammond, Gerald B
author_sort Liu, Leping
collection PubMed
description During the last decade, gold-catalyzed reactions have become a tour de force in organic synthesis. Recently, the gold-, Brønsted acid- or Lewis acid-catalyzed oxygen transfer from carbonyl to carbon–carbon triple bond, the so-called alkyne–carbonyl metathesis, has attracted much attention because this atom economical transformation generates α,β-unsaturated carbonyl derivatives which are of great interest in synthetic organic chemistry. This mini-review focuses on the most recent achievements on gold-catalyzed oxygen transfer reactions of tethered alkynones, diynes or alkynyl epoxides to cyclic enones. The corresponding mechanisms for the transformations are also discussed.
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spelling pubmed-31075342011-06-06 Construction of cyclic enones via gold-catalyzed oxygen transfer reactions Liu, Leping Xu, Bo Hammond, Gerald B Beilstein J Org Chem Review During the last decade, gold-catalyzed reactions have become a tour de force in organic synthesis. Recently, the gold-, Brønsted acid- or Lewis acid-catalyzed oxygen transfer from carbonyl to carbon–carbon triple bond, the so-called alkyne–carbonyl metathesis, has attracted much attention because this atom economical transformation generates α,β-unsaturated carbonyl derivatives which are of great interest in synthetic organic chemistry. This mini-review focuses on the most recent achievements on gold-catalyzed oxygen transfer reactions of tethered alkynones, diynes or alkynyl epoxides to cyclic enones. The corresponding mechanisms for the transformations are also discussed. Beilstein-Institut 2011-05-13 /pmc/articles/PMC3107534/ /pubmed/21647265 http://dx.doi.org/10.3762/bjoc.7.71 Text en Copyright © 2011, Liu et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Liu, Leping
Xu, Bo
Hammond, Gerald B
Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title_full Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title_fullStr Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title_full_unstemmed Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title_short Construction of cyclic enones via gold-catalyzed oxygen transfer reactions
title_sort construction of cyclic enones via gold-catalyzed oxygen transfer reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107534/
https://www.ncbi.nlm.nih.gov/pubmed/21647265
http://dx.doi.org/10.3762/bjoc.7.71
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