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Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction

Medium sized carbocycles are particularly difficult to synthesize. Ring closing metathesis reactions (RCM) have recently been applied to construct eight-membered carbocycles, but trisubstituted double bonds in the eight-membered rings are more difficult to produce using RCM reactions. In this review...

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Detalles Bibliográficos
Autores principales: Tori, Motoo, Mizutani, Reiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264272/
https://www.ncbi.nlm.nih.gov/pubmed/20657438
http://dx.doi.org/10.3390/molecules15064242
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author Tori, Motoo
Mizutani, Reiko
author_facet Tori, Motoo
Mizutani, Reiko
author_sort Tori, Motoo
collection PubMed
description Medium sized carbocycles are particularly difficult to synthesize. Ring closing metathesis reactions (RCM) have recently been applied to construct eight-membered carbocycles, but trisubstituted double bonds in the eight-membered rings are more difficult to produce using RCM reactions. In this review, model examples and our own results are cited and the importance of the preparation of suitably designed precursors is discussed. Examples of RCM reactions used in the total synthesis of natural products are also outlined.
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spelling pubmed-62642722018-12-04 Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction Tori, Motoo Mizutani, Reiko Molecules Review Medium sized carbocycles are particularly difficult to synthesize. Ring closing metathesis reactions (RCM) have recently been applied to construct eight-membered carbocycles, but trisubstituted double bonds in the eight-membered rings are more difficult to produce using RCM reactions. In this review, model examples and our own results are cited and the importance of the preparation of suitably designed precursors is discussed. Examples of RCM reactions used in the total synthesis of natural products are also outlined. MDPI 2010-06-11 /pmc/articles/PMC6264272/ /pubmed/20657438 http://dx.doi.org/10.3390/molecules15064242 Text en © 2010 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Tori, Motoo
Mizutani, Reiko
Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title_full Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title_fullStr Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title_full_unstemmed Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title_short Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction
title_sort construction of eight-membered carbocycles with trisubstituted double bonds using the ring closing metathesis reaction
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264272/
https://www.ncbi.nlm.nih.gov/pubmed/20657438
http://dx.doi.org/10.3390/molecules15064242
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AT mizutanireiko constructionofeightmemberedcarbocycleswithtrisubstituteddoublebondsusingtheringclosingmetathesisreaction