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A Universal Isocyanide for Diverse Heterocycle Syntheses
[Image: see text] Novel scaffolds are of uttermost importance for the discovery of functional material. Three different heterocyclic scaffolds easily accessible from isocyanoacetaldehyde dimethylacetal 1 by multicomponent reaction (MCR) are described. They can be efficiently synthesized by a Ugi tet...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227542/ https://www.ncbi.nlm.nih.gov/pubmed/25351886 http://dx.doi.org/10.1021/ol5024882 |
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author | Patil, Pravin Khoury, Kareem Herdtweck, Eberhardt Dömling, Alexander |
author_facet | Patil, Pravin Khoury, Kareem Herdtweck, Eberhardt Dömling, Alexander |
author_sort | Patil, Pravin |
collection | PubMed |
description | [Image: see text] Novel scaffolds are of uttermost importance for the discovery of functional material. Three different heterocyclic scaffolds easily accessible from isocyanoacetaldehyde dimethylacetal 1 by multicomponent reaction (MCR) are described. They can be efficiently synthesized by a Ugi tetrazole multicomponent reaction of 1. We discuss the synthesis, 3D structures, and other physicochemical properties. |
format | Online Article Text |
id | pubmed-4227542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42275422015-10-29 A Universal Isocyanide for Diverse Heterocycle Syntheses Patil, Pravin Khoury, Kareem Herdtweck, Eberhardt Dömling, Alexander Org Lett [Image: see text] Novel scaffolds are of uttermost importance for the discovery of functional material. Three different heterocyclic scaffolds easily accessible from isocyanoacetaldehyde dimethylacetal 1 by multicomponent reaction (MCR) are described. They can be efficiently synthesized by a Ugi tetrazole multicomponent reaction of 1. We discuss the synthesis, 3D structures, and other physicochemical properties. American Chemical Society 2014-10-29 2014-11-07 /pmc/articles/PMC4227542/ /pubmed/25351886 http://dx.doi.org/10.1021/ol5024882 Text en Copyright © 2014 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 | Patil, Pravin Khoury, Kareem Herdtweck, Eberhardt Dömling, Alexander A Universal Isocyanide for Diverse Heterocycle Syntheses |
title | A Universal Isocyanide for Diverse Heterocycle Syntheses |
title_full | A Universal Isocyanide for Diverse Heterocycle Syntheses |
title_fullStr | A Universal Isocyanide for Diverse Heterocycle Syntheses |
title_full_unstemmed | A Universal Isocyanide for Diverse Heterocycle Syntheses |
title_short | A Universal Isocyanide for Diverse Heterocycle Syntheses |
title_sort | universal isocyanide for diverse heterocycle syntheses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227542/ https://www.ncbi.nlm.nih.gov/pubmed/25351886 http://dx.doi.org/10.1021/ol5024882 |
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