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Redox-Annulation of Cyclic Amines and β-Ketoaldehydes
[Image: see text] Benzo[a]quinolizine-2-one derivatives are readily assembled from 1,2,3,4-tetrahydroisoquinoline and β-ketoaldehydes by means of a new intramolecular redox-Mannich process. These reactions are promoted by simple acetic acid and are thought to involve azomethine ylides as reactive in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782176/ https://www.ncbi.nlm.nih.gov/pubmed/26895555 http://dx.doi.org/10.1021/acs.orglett.6b00151 |
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author | Chen, Weijie Seidel, Daniel |
author_facet | Chen, Weijie Seidel, Daniel |
author_sort | Chen, Weijie |
collection | PubMed |
description | [Image: see text] Benzo[a]quinolizine-2-one derivatives are readily assembled from 1,2,3,4-tetrahydroisoquinoline and β-ketoaldehydes by means of a new intramolecular redox-Mannich process. These reactions are promoted by simple acetic acid and are thought to involve azomethine ylides as reactive intermediates. |
format | Online Article Text |
id | pubmed-4782176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47821762016-03-09 Redox-Annulation of Cyclic Amines and β-Ketoaldehydes Chen, Weijie Seidel, Daniel Org Lett [Image: see text] Benzo[a]quinolizine-2-one derivatives are readily assembled from 1,2,3,4-tetrahydroisoquinoline and β-ketoaldehydes by means of a new intramolecular redox-Mannich process. These reactions are promoted by simple acetic acid and are thought to involve azomethine ylides as reactive intermediates. American Chemical Society 2016-02-19 2016-03-04 /pmc/articles/PMC4782176/ /pubmed/26895555 http://dx.doi.org/10.1021/acs.orglett.6b00151 Text en Copyright © 2016 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 | Chen, Weijie Seidel, Daniel Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title | Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title_full | Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title_fullStr | Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title_full_unstemmed | Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title_short | Redox-Annulation of Cyclic Amines and β-Ketoaldehydes |
title_sort | redox-annulation of cyclic amines and β-ketoaldehydes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782176/ https://www.ncbi.nlm.nih.gov/pubmed/26895555 http://dx.doi.org/10.1021/acs.orglett.6b00151 |
work_keys_str_mv | AT chenweijie redoxannulationofcyclicaminesandbketoaldehydes AT seideldaniel redoxannulationofcyclicaminesandbketoaldehydes |