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Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules
This review covers recent advances in synthesis of azocine-containing systems. The most approaches towards azocines are discussed. 1 Introduction 2 Ring-Expansion Reaction 2.1 Ring-Expansion Reaction of Cyclopentane Containing the 1,4-Diketone Moiety with Primary Amines (from 5 to 8) 2.2 Ring-Expans...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
© Georg Thieme Verlag
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376628/ http://dx.doi.org/10.1055/s-0036-1589500 |
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author | Listratova, Anna V. Voskressensky, Leonid G. |
author_facet | Listratova, Anna V. Voskressensky, Leonid G. |
author_sort | Listratova, Anna V. |
collection | PubMed |
description | This review covers recent advances in synthesis of azocine-containing systems. The most approaches towards azocines are discussed. 1 Introduction 2 Ring-Expansion Reaction 2.1 Ring-Expansion Reaction of Cyclopentane Containing the 1,4-Diketone Moiety with Primary Amines (from 5 to 8) 2.2 Ring-Expansion Reaction of Annulated Tetrahydropyridines under the Action of Activated Alkynes (from 6 to 8) 2.3 Reductive Ring-Expansion Reaction of Cyclic Oximes 2.4 Other Ring-Expansion Reactions 3 Heck Reaction 4 Cycloaddition 5 Ring-Closing Metathesis (RCM) 6 Cyclization 6.1 Metal-Catalyzed Cyclization 6.2 Radical Cyclization 6.3 Friedel–Crafts Cyclization 6.4 Other Examples of Cyclizations 7 Microwave- and Photo-Assisted Reactions 8 Other Methods 8.1 Cascade and Tandem Reactions 8.2 Aldol Condensation 8.3 Thermolysis 8.4 Ring Opening 8.5 Other Methods 9 Conclusion |
format | Online Article Text |
id | pubmed-6376628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | © Georg Thieme Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-63766282019-02-19 Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules Listratova, Anna V. Voskressensky, Leonid G. Synthesis (Stuttg) This review covers recent advances in synthesis of azocine-containing systems. The most approaches towards azocines are discussed. 1 Introduction 2 Ring-Expansion Reaction 2.1 Ring-Expansion Reaction of Cyclopentane Containing the 1,4-Diketone Moiety with Primary Amines (from 5 to 8) 2.2 Ring-Expansion Reaction of Annulated Tetrahydropyridines under the Action of Activated Alkynes (from 6 to 8) 2.3 Reductive Ring-Expansion Reaction of Cyclic Oximes 2.4 Other Ring-Expansion Reactions 3 Heck Reaction 4 Cycloaddition 5 Ring-Closing Metathesis (RCM) 6 Cyclization 6.1 Metal-Catalyzed Cyclization 6.2 Radical Cyclization 6.3 Friedel–Crafts Cyclization 6.4 Other Examples of Cyclizations 7 Microwave- and Photo-Assisted Reactions 8 Other Methods 8.1 Cascade and Tandem Reactions 8.2 Aldol Condensation 8.3 Thermolysis 8.4 Ring Opening 8.5 Other Methods 9 Conclusion © Georg Thieme Verlag 2017-09-01 2017-08-01 /pmc/articles/PMC6376628/ http://dx.doi.org/10.1055/s-0036-1589500 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Listratova, Anna V. Voskressensky, Leonid G. Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title | Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title_full | Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title_fullStr | Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title_full_unstemmed | Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title_short | Recent Advances in the Synthesis of Hydrogenated Azocine-Containing Molecules |
title_sort | recent advances in the synthesis of hydrogenated azocine-containing molecules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376628/ http://dx.doi.org/10.1055/s-0036-1589500 |
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