Strategies in the synthesis of dibenzo[b,f]heteropines

The dibenzo[b,f]azepine skeleton is important in the pharmaceutical industry, not only in terms of existing commercial antidepressants, anxiolytics and anticonvulsants, but also in reengineering for other applications. More recently, the potential of the dibenzo[b,f]azepine moiety in organic light e...

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Autores principales: Maier, David Irving Hermann, Bezuidenhoudt, Barend Christiaan Buurman, Marais, Charlene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241096/
https://www.ncbi.nlm.nih.gov/pubmed/37284586
http://dx.doi.org/10.3762/bjoc.19.51
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author Maier, David Irving Hermann
Bezuidenhoudt, Barend Christiaan Buurman
Marais, Charlene
author_facet Maier, David Irving Hermann
Bezuidenhoudt, Barend Christiaan Buurman
Marais, Charlene
author_sort Maier, David Irving Hermann
collection PubMed
description The dibenzo[b,f]azepine skeleton is important in the pharmaceutical industry, not only in terms of existing commercial antidepressants, anxiolytics and anticonvulsants, but also in reengineering for other applications. More recently, the potential of the dibenzo[b,f]azepine moiety in organic light emitting diodes and dye-sensitized solar cell dyes has been recognised, while catalysts and molecular organic frameworks with dibenzo[b,f]azepine derived ligands have also been reported. This review provides a brief overview of the different synthetic strategies to dibenzo[b,f]azepines and other dibenzo[b,f]heteropines.
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spelling pubmed-102410962023-06-06 Strategies in the synthesis of dibenzo[b,f]heteropines Maier, David Irving Hermann Bezuidenhoudt, Barend Christiaan Buurman Marais, Charlene Beilstein J Org Chem Review The dibenzo[b,f]azepine skeleton is important in the pharmaceutical industry, not only in terms of existing commercial antidepressants, anxiolytics and anticonvulsants, but also in reengineering for other applications. More recently, the potential of the dibenzo[b,f]azepine moiety in organic light emitting diodes and dye-sensitized solar cell dyes has been recognised, while catalysts and molecular organic frameworks with dibenzo[b,f]azepine derived ligands have also been reported. This review provides a brief overview of the different synthetic strategies to dibenzo[b,f]azepines and other dibenzo[b,f]heteropines. Beilstein-Institut 2023-05-22 /pmc/articles/PMC10241096/ /pubmed/37284586 http://dx.doi.org/10.3762/bjoc.19.51 Text en Copyright © 2023, Maier et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.
spellingShingle Review
Maier, David Irving Hermann
Bezuidenhoudt, Barend Christiaan Buurman
Marais, Charlene
Strategies in the synthesis of dibenzo[b,f]heteropines
title Strategies in the synthesis of dibenzo[b,f]heteropines
title_full Strategies in the synthesis of dibenzo[b,f]heteropines
title_fullStr Strategies in the synthesis of dibenzo[b,f]heteropines
title_full_unstemmed Strategies in the synthesis of dibenzo[b,f]heteropines
title_short Strategies in the synthesis of dibenzo[b,f]heteropines
title_sort strategies in the synthesis of dibenzo[b,f]heteropines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241096/
https://www.ncbi.nlm.nih.gov/pubmed/37284586
http://dx.doi.org/10.3762/bjoc.19.51
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