Cargando…

Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams

New gold-catalyzed methods using the β-lactam scaffold have been recently developed for the synthesis of different sized heterocycles. This overview focuses on heterocyclization reactions of allenic and alkynic β-lactams which rely on the activation of the allene and alkyne component. The mechanism...

Descripción completa

Detalles Bibliográficos
Autores principales: Alcaide, Benito, Almendros, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107458/
https://www.ncbi.nlm.nih.gov/pubmed/21647323
http://dx.doi.org/10.3762/bjoc.7.73
_version_ 1782205225375891456
author Alcaide, Benito
Almendros, Pedro
author_facet Alcaide, Benito
Almendros, Pedro
author_sort Alcaide, Benito
collection PubMed
description New gold-catalyzed methods using the β-lactam scaffold have been recently developed for the synthesis of different sized heterocycles. This overview focuses on heterocyclization reactions of allenic and alkynic β-lactams which rely on the activation of the allene and alkyne component. The mechanism as well as the regio- and stereoselectivity of the cyclizations are also discussed.
format Online
Article
Text
id pubmed-3107458
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-31074582011-06-06 Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams Alcaide, Benito Almendros, Pedro Beilstein J Org Chem Review New gold-catalyzed methods using the β-lactam scaffold have been recently developed for the synthesis of different sized heterocycles. This overview focuses on heterocyclization reactions of allenic and alkynic β-lactams which rely on the activation of the allene and alkyne component. The mechanism as well as the regio- and stereoselectivity of the cyclizations are also discussed. Beilstein-Institut 2011-05-17 /pmc/articles/PMC3107458/ /pubmed/21647323 http://dx.doi.org/10.3762/bjoc.7.73 Text en Copyright © 2011, Alcaide and Almendros 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
Alcaide, Benito
Almendros, Pedro
Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title_full Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title_fullStr Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title_full_unstemmed Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title_short Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
title_sort gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107458/
https://www.ncbi.nlm.nih.gov/pubmed/21647323
http://dx.doi.org/10.3762/bjoc.7.73
work_keys_str_mv AT alcaidebenito goldcatalyzedheterocyclizationsinalkynylandallenylblactams
AT almendrospedro goldcatalyzedheterocyclizationsinalkynylandallenylblactams