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Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition
Peculiarities of [8+2] cycloaddition of acetylenes to indolizines are reviewed. Especially mentioned are indolizines with leaving groups at positions 3 and 5. Cycloaddition to aza- and benzo derivatives are reviewed, as well as 1,10-cyclizations and processes leading to cyclazines where indolizines...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038407/ https://www.ncbi.nlm.nih.gov/pubmed/33916655 http://dx.doi.org/10.3390/molecules26072050 |
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author | Babaev, Eugene V. Shadrin, Ivan A. |
author_facet | Babaev, Eugene V. Shadrin, Ivan A. |
author_sort | Babaev, Eugene V. |
collection | PubMed |
description | Peculiarities of [8+2] cycloaddition of acetylenes to indolizines are reviewed. Especially mentioned are indolizines with leaving groups at positions 3 and 5. Cycloaddition to aza- and benzo derivatives are reviewed, as well as 1,10-cyclizations and processes leading to cyclazines where indolizines are intermediates. Mechanistic features (adducts and cycloadducts) and theoretical aspects (one- or two-steps mechanism) are reviewed. |
format | Online Article Text |
id | pubmed-8038407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80384072021-04-12 Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition Babaev, Eugene V. Shadrin, Ivan A. Molecules Review Peculiarities of [8+2] cycloaddition of acetylenes to indolizines are reviewed. Especially mentioned are indolizines with leaving groups at positions 3 and 5. Cycloaddition to aza- and benzo derivatives are reviewed, as well as 1,10-cyclizations and processes leading to cyclazines where indolizines are intermediates. Mechanistic features (adducts and cycloadducts) and theoretical aspects (one- or two-steps mechanism) are reviewed. MDPI 2021-04-03 /pmc/articles/PMC8038407/ /pubmed/33916655 http://dx.doi.org/10.3390/molecules26072050 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Babaev, Eugene V. Shadrin, Ivan A. Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title | Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title_full | Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title_fullStr | Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title_full_unstemmed | Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title_short | Indolizines and Their Hetero/Benzo Derivatives in Reactions of [8+2] Cycloaddition |
title_sort | indolizines and their hetero/benzo derivatives in reactions of [8+2] cycloaddition |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038407/ https://www.ncbi.nlm.nih.gov/pubmed/33916655 http://dx.doi.org/10.3390/molecules26072050 |
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