Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes

Organocatalysis constitutes one of the main research areas in organic chemistry from the last two decades. This chemistry has been applied to the synthesis of many natural products and structures in a manner that reduces the residues and so the ecological impact. In this review, we consider the work...

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Autores principales: Tobal, Ignacio E., Roncero, Alejandro M., Garrido, Narciso M., Marcos, Isidro S., Díez, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099548/
https://www.ncbi.nlm.nih.gov/pubmed/29710794
http://dx.doi.org/10.3390/molecules23051039
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author Tobal, Ignacio E.
Roncero, Alejandro M.
Garrido, Narciso M.
Marcos, Isidro S.
Díez, David
author_facet Tobal, Ignacio E.
Roncero, Alejandro M.
Garrido, Narciso M.
Marcos, Isidro S.
Díez, David
author_sort Tobal, Ignacio E.
collection PubMed
description Organocatalysis constitutes one of the main research areas in organic chemistry from the last two decades. This chemistry has been applied to the synthesis of many natural products and structures in a manner that reduces the residues and so the ecological impact. In this review, we consider the work that has been done for the synthesis of bicyclo[3.2.1]octane framework. This structure is present in many natural products with very important biological activities.
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spelling pubmed-60995482018-11-13 Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes Tobal, Ignacio E. Roncero, Alejandro M. Garrido, Narciso M. Marcos, Isidro S. Díez, David Molecules Review Organocatalysis constitutes one of the main research areas in organic chemistry from the last two decades. This chemistry has been applied to the synthesis of many natural products and structures in a manner that reduces the residues and so the ecological impact. In this review, we consider the work that has been done for the synthesis of bicyclo[3.2.1]octane framework. This structure is present in many natural products with very important biological activities. MDPI 2018-04-28 /pmc/articles/PMC6099548/ /pubmed/29710794 http://dx.doi.org/10.3390/molecules23051039 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tobal, Ignacio E.
Roncero, Alejandro M.
Garrido, Narciso M.
Marcos, Isidro S.
Díez, David
Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title_full Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title_fullStr Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title_full_unstemmed Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title_short Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes
title_sort organocatalyzed synthesis of [3.2.1] bicyclooctanes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099548/
https://www.ncbi.nlm.nih.gov/pubmed/29710794
http://dx.doi.org/10.3390/molecules23051039
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