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Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes)
Different strategies for the racemic or enantiospecific total syntheses of plant and mammalian 3,4-dibenzyltetrahydrofuran lignans are reviewed and compared. The multi-step approaches have various key step strategies: Diels–Alder reactions, Stobbe condensations, Michael additions, alkylations, nitri...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270424/ https://www.ncbi.nlm.nih.gov/pubmed/24284480 http://dx.doi.org/10.3390/molecules181113124 |
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author | Pohjoispää, Monika Wähälä, Kristiina |
author_facet | Pohjoispää, Monika Wähälä, Kristiina |
author_sort | Pohjoispää, Monika |
collection | PubMed |
description | Different strategies for the racemic or enantiospecific total syntheses of plant and mammalian 3,4-dibenzyltetrahydrofuran lignans are reviewed and compared. The multi-step approaches have various key step strategies: Diels–Alder reactions, Stobbe condensations, Michael additions, alkylations, nitrile oxide cycloadditions, radical cyclisations, dianion and oxidative couplings. |
format | Online Article Text |
id | pubmed-6270424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62704242018-12-20 Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) Pohjoispää, Monika Wähälä, Kristiina Molecules Review Different strategies for the racemic or enantiospecific total syntheses of plant and mammalian 3,4-dibenzyltetrahydrofuran lignans are reviewed and compared. The multi-step approaches have various key step strategies: Diels–Alder reactions, Stobbe condensations, Michael additions, alkylations, nitrile oxide cycloadditions, radical cyclisations, dianion and oxidative couplings. MDPI 2013-10-24 /pmc/articles/PMC6270424/ /pubmed/24284480 http://dx.doi.org/10.3390/molecules181113124 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 Pohjoispää, Monika Wähälä, Kristiina Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title | Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title_full | Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title_fullStr | Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title_full_unstemmed | Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title_short | Synthesis of 3,4-Dibenzyltetrahydrofuran Lignans (9,9′-Epoxylignanes) |
title_sort | synthesis of 3,4-dibenzyltetrahydrofuran lignans (9,9′-epoxylignanes) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270424/ https://www.ncbi.nlm.nih.gov/pubmed/24284480 http://dx.doi.org/10.3390/molecules181113124 |
work_keys_str_mv | AT pohjoispaamonika synthesisof34dibenzyltetrahydrofuranlignans99epoxylignanes AT wahalakristiina synthesisof34dibenzyltetrahydrofuranlignans99epoxylignanes |