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Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol
[Image: see text] The four-step procedure involving bromination, reduction, and nucleophilic substitution via elimination/addition previously applied to 1-(2-pyridyl)-2-propen-1-ol for the synthesis of indolizidine systems has now been extended to 1-(2-quinolyl)-2-propen-1-ol allowing a general acce...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641500/ https://www.ncbi.nlm.nih.gov/pubmed/31458576 http://dx.doi.org/10.1021/acsomega.8b00167 |
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author | Giomi, Donatella Ceccarelli, Jacopo Brandi, Alberto |
author_facet | Giomi, Donatella Ceccarelli, Jacopo Brandi, Alberto |
author_sort | Giomi, Donatella |
collection | PubMed |
description | [Image: see text] The four-step procedure involving bromination, reduction, and nucleophilic substitution via elimination/addition previously applied to 1-(2-pyridyl)-2-propen-1-ol for the synthesis of indolizidine systems has now been extended to 1-(2-quinolyl)-2-propen-1-ol allowing a general access to benzo-fused derivatives. For instance, (±)-benzo[e]lentiginosine has been easily synthesized in an 18% overall yield. |
format | Online Article Text |
id | pubmed-6641500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66415002019-08-27 Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol Giomi, Donatella Ceccarelli, Jacopo Brandi, Alberto ACS Omega [Image: see text] The four-step procedure involving bromination, reduction, and nucleophilic substitution via elimination/addition previously applied to 1-(2-pyridyl)-2-propen-1-ol for the synthesis of indolizidine systems has now been extended to 1-(2-quinolyl)-2-propen-1-ol allowing a general access to benzo-fused derivatives. For instance, (±)-benzo[e]lentiginosine has been easily synthesized in an 18% overall yield. American Chemical Society 2018-03-15 /pmc/articles/PMC6641500/ /pubmed/31458576 http://dx.doi.org/10.1021/acsomega.8b00167 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Giomi, Donatella Ceccarelli, Jacopo Brandi, Alberto Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title | Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title_full | Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title_fullStr | Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title_full_unstemmed | Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title_short | Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol |
title_sort | synthesis of new indolizidine derivatives from 1-(2-quinolyl)-2-propen-1-ol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641500/ https://www.ncbi.nlm.nih.gov/pubmed/31458576 http://dx.doi.org/10.1021/acsomega.8b00167 |
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