Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives

The reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated c...

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Detalles Bibliográficos
Autores principales: Masesane, Ishmael B, Desta, Zelalem Yibralign
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554813/
https://www.ncbi.nlm.nih.gov/pubmed/23365628
http://dx.doi.org/10.3762/bjoc.8.244
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author Masesane, Ishmael B
Desta, Zelalem Yibralign
author_facet Masesane, Ishmael B
Desta, Zelalem Yibralign
author_sort Masesane, Ishmael B
collection PubMed
description The reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated compounds.
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spelling pubmed-35548132013-01-30 Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives Masesane, Ishmael B Desta, Zelalem Yibralign Beilstein J Org Chem Review The reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated compounds. Beilstein-Institut 2012-12-12 /pmc/articles/PMC3554813/ /pubmed/23365628 http://dx.doi.org/10.3762/bjoc.8.244 Text en Copyright © 2012, Masesane and Desta 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
Masesane, Ishmael B
Desta, Zelalem Yibralign
Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title_full Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title_fullStr Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title_full_unstemmed Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title_short Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
title_sort reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554813/
https://www.ncbi.nlm.nih.gov/pubmed/23365628
http://dx.doi.org/10.3762/bjoc.8.244
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AT destazelalemyibralign reactionsofsalicylaldehydeandenolatesortheirequivalentsversatilesyntheticroutestochromanederivatives

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