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Acceptorless Dehydrogenative Coupling Using Ammonia: Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium
[Image: see text] The synthesis of N-heteroaromatic compounds via an acceptorless dehydrogenative coupling process involving direct use of ammonia as the nitrogen source was explored. We report the synthesis of pyrazine derivatives from 1,2-diols and the synthesis of N-substituted pyrroles by a mult...
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/PMC6502445/ https://www.ncbi.nlm.nih.gov/pubmed/30205675 http://dx.doi.org/10.1021/jacs.8b08385 |
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author | Daw, Prosenjit Ben-David, Yehoshoa Milstein, David |
author_facet | Daw, Prosenjit Ben-David, Yehoshoa Milstein, David |
author_sort | Daw, Prosenjit |
collection | PubMed |
description | [Image: see text] The synthesis of N-heteroaromatic compounds via an acceptorless dehydrogenative coupling process involving direct use of ammonia as the nitrogen source was explored. We report the synthesis of pyrazine derivatives from 1,2-diols and the synthesis of N-substituted pyrroles by a multicomponent dehydrogenative coupling of 1,4-diols and primary alcohols with ammonia. The acridine-based Ru-pincer complex 1 is an effective catalyst for these transformations, in which the acridine backbone is converted to an anionic dearomatized PNP-pincer ligand framework. |
format | Online Article Text |
id | pubmed-6502445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65024452019-05-08 Acceptorless Dehydrogenative Coupling Using Ammonia: Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium Daw, Prosenjit Ben-David, Yehoshoa Milstein, David J Am Chem Soc [Image: see text] The synthesis of N-heteroaromatic compounds via an acceptorless dehydrogenative coupling process involving direct use of ammonia as the nitrogen source was explored. We report the synthesis of pyrazine derivatives from 1,2-diols and the synthesis of N-substituted pyrroles by a multicomponent dehydrogenative coupling of 1,4-diols and primary alcohols with ammonia. The acridine-based Ru-pincer complex 1 is an effective catalyst for these transformations, in which the acridine backbone is converted to an anionic dearomatized PNP-pincer ligand framework. American Chemical Society 2018-09-12 2018-09-26 /pmc/articles/PMC6502445/ /pubmed/30205675 http://dx.doi.org/10.1021/jacs.8b08385 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 | Daw, Prosenjit Ben-David, Yehoshoa Milstein, David Acceptorless Dehydrogenative Coupling Using Ammonia: Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium |
title | Acceptorless
Dehydrogenative Coupling Using Ammonia:
Direct Synthesis of N-Heteroaromatics from Diols Catalyzed
by Ruthenium |
title_full | Acceptorless
Dehydrogenative Coupling Using Ammonia:
Direct Synthesis of N-Heteroaromatics from Diols Catalyzed
by Ruthenium |
title_fullStr | Acceptorless
Dehydrogenative Coupling Using Ammonia:
Direct Synthesis of N-Heteroaromatics from Diols Catalyzed
by Ruthenium |
title_full_unstemmed | Acceptorless
Dehydrogenative Coupling Using Ammonia:
Direct Synthesis of N-Heteroaromatics from Diols Catalyzed
by Ruthenium |
title_short | Acceptorless
Dehydrogenative Coupling Using Ammonia:
Direct Synthesis of N-Heteroaromatics from Diols Catalyzed
by Ruthenium |
title_sort | acceptorless
dehydrogenative coupling using ammonia:
direct synthesis of n-heteroaromatics from diols catalyzed
by ruthenium |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502445/ https://www.ncbi.nlm.nih.gov/pubmed/30205675 http://dx.doi.org/10.1021/jacs.8b08385 |
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