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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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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. |
format | Online Article Text |
id | pubmed-3596099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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