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Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes

[Image: see text] We report the regioselective synthesis of silyl-substituted cyclopentadienyl esters through gold-catalyzed migratory cycloisomerization of silyl-substituted vinylallenes. This transformation is proposed to proceed through a perfectly orchestrated sequence of events including Nazaro...

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Autores principales: Bernardo, Olaya, González, Javier, Borge, Javier, López, Luis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490818/
https://www.ncbi.nlm.nih.gov/pubmed/35819017
http://dx.doi.org/10.1021/acs.orglett.2c02035
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author Bernardo, Olaya
González, Javier
Borge, Javier
López, Luis A.
author_facet Bernardo, Olaya
González, Javier
Borge, Javier
López, Luis A.
author_sort Bernardo, Olaya
collection PubMed
description [Image: see text] We report the regioselective synthesis of silyl-substituted cyclopentadienyl esters through gold-catalyzed migratory cycloisomerization of silyl-substituted vinylallenes. This transformation is proposed to proceed through a perfectly orchestrated sequence of events including Nazarov-like cyclization and several silyl and hydrogen rearrangements. Furthermore, exploiting the multifaceted nature of the gold catalyst, we have also identified suitable conditions for the synthesis of these cyclopentadienes in a more straightforward manner through gold-catalyzed reaction of propargyl esters and alkynylsilanes.
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spelling pubmed-94908182022-09-22 Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes Bernardo, Olaya González, Javier Borge, Javier López, Luis A. Org Lett [Image: see text] We report the regioselective synthesis of silyl-substituted cyclopentadienyl esters through gold-catalyzed migratory cycloisomerization of silyl-substituted vinylallenes. This transformation is proposed to proceed through a perfectly orchestrated sequence of events including Nazarov-like cyclization and several silyl and hydrogen rearrangements. Furthermore, exploiting the multifaceted nature of the gold catalyst, we have also identified suitable conditions for the synthesis of these cyclopentadienes in a more straightforward manner through gold-catalyzed reaction of propargyl esters and alkynylsilanes. American Chemical Society 2022-07-12 2022-07-22 /pmc/articles/PMC9490818/ /pubmed/35819017 http://dx.doi.org/10.1021/acs.orglett.2c02035 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Bernardo, Olaya
González, Javier
Borge, Javier
López, Luis A.
Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title_full Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title_fullStr Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title_full_unstemmed Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title_short Gold-Catalyzed Regioselective Synthesis of Crowded Cyclopentadienes by Migratory Cycloisomerization of Vinylallenes
title_sort gold-catalyzed regioselective synthesis of crowded cyclopentadienes by migratory cycloisomerization of vinylallenes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490818/
https://www.ncbi.nlm.nih.gov/pubmed/35819017
http://dx.doi.org/10.1021/acs.orglett.2c02035
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