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Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes

The palladium(ii)-catalyzed carbocyclization of benzenecarbaldehydes with internal alkynes to afford 2,3-disubstituted indenones was reported. The annulation reaction proceeded through the transmetalation of Pd(ii) with an aromatic aldehyde and the insertion of internal alkynes, followed by cyclizat...

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Autores principales: Kashanna, Jajula, Aravind Kumar, Rathod, Kishore, Ravada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072296/
https://www.ncbi.nlm.nih.gov/pubmed/35529398
http://dx.doi.org/10.1039/c9ra03921j
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author Kashanna, Jajula
Aravind Kumar, Rathod
Kishore, Ravada
author_facet Kashanna, Jajula
Aravind Kumar, Rathod
Kishore, Ravada
author_sort Kashanna, Jajula
collection PubMed
description The palladium(ii)-catalyzed carbocyclization of benzenecarbaldehydes with internal alkynes to afford 2,3-disubstituted indenones was reported. The annulation reaction proceeded through the transmetalation of Pd(ii) with an aromatic aldehyde and the insertion of internal alkynes, followed by cyclization via the intramolecular nucleophilic addition of intermediate organopalladium(ii) species to the aldehyde group. This reaction proceeded in moderate to good yields with high regioselectivity.
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spelling pubmed-90722962022-05-06 Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes Kashanna, Jajula Aravind Kumar, Rathod Kishore, Ravada RSC Adv Chemistry The palladium(ii)-catalyzed carbocyclization of benzenecarbaldehydes with internal alkynes to afford 2,3-disubstituted indenones was reported. The annulation reaction proceeded through the transmetalation of Pd(ii) with an aromatic aldehyde and the insertion of internal alkynes, followed by cyclization via the intramolecular nucleophilic addition of intermediate organopalladium(ii) species to the aldehyde group. This reaction proceeded in moderate to good yields with high regioselectivity. The Royal Society of Chemistry 2019-10-02 /pmc/articles/PMC9072296/ /pubmed/35529398 http://dx.doi.org/10.1039/c9ra03921j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kashanna, Jajula
Aravind Kumar, Rathod
Kishore, Ravada
Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title_full Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title_fullStr Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title_full_unstemmed Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title_short Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
title_sort palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072296/
https://www.ncbi.nlm.nih.gov/pubmed/35529398
http://dx.doi.org/10.1039/c9ra03921j
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