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Inter- and intramolecular enantioselective carbolithiation reactions

In this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (−)-sparteine, to promote facial selection on a C=C bond. This is an attractive approach for the construction of...

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Detalles Bibliográficos
Autores principales: Gómez-SanJuan, Asier, Sotomayor, Nuria, Lete, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596099/
https://www.ncbi.nlm.nih.gov/pubmed/23504613
http://dx.doi.org/10.3762/bjoc.9.36
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author Gómez-SanJuan, Asier
Sotomayor, Nuria
Lete, Esther
author_facet Gómez-SanJuan, Asier
Sotomayor, Nuria
Lete, Esther
author_sort Gómez-SanJuan, Asier
collection PubMed
description In this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (−)-sparteine, to promote facial selection on a C=C bond. This is an attractive approach for the construction of new carbon–carbon bonds in an asymmetric fashion, with the possibility of introducing further functionalization on the molecule by trapping the reactive organolithium intermediates with electrophiles.
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spelling pubmed-35960992013-03-15 Inter- and intramolecular enantioselective carbolithiation reactions Gómez-SanJuan, Asier Sotomayor, Nuria Lete, Esther Beilstein J Org Chem Review In this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (−)-sparteine, to promote facial selection on a C=C bond. This is an attractive approach for the construction of new carbon–carbon bonds in an asymmetric fashion, with the possibility of introducing further functionalization on the molecule by trapping the reactive organolithium intermediates with electrophiles. Beilstein-Institut 2013-02-13 /pmc/articles/PMC3596099/ /pubmed/23504613 http://dx.doi.org/10.3762/bjoc.9.36 Text en Copyright © 2013, Gómez-SanJuan 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
Gómez-SanJuan, Asier
Sotomayor, Nuria
Lete, Esther
Inter- and intramolecular enantioselective carbolithiation reactions
title Inter- and intramolecular enantioselective carbolithiation reactions
title_full Inter- and intramolecular enantioselective carbolithiation reactions
title_fullStr Inter- and intramolecular enantioselective carbolithiation reactions
title_full_unstemmed Inter- and intramolecular enantioselective carbolithiation reactions
title_short Inter- and intramolecular enantioselective carbolithiation reactions
title_sort inter- and intramolecular enantioselective carbolithiation reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596099/
https://www.ncbi.nlm.nih.gov/pubmed/23504613
http://dx.doi.org/10.3762/bjoc.9.36
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