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.
Journal article
Acceptorless Dehydrogenative Coupling Using Ammonia: Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium
Journal of the American Chemical Society, Vol.140(38), pp.11931-11934
26/Sep/2018
Abstract
Details
- Title
- Acceptorless Dehydrogenative Coupling Using Ammonia; Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium
- Creators
- Prosenjit Daw (null) - The Weizmann Institute of Science, Department of Organic ChemistryYehoshoa Ben-David (null) - The Weizmann Institute of Science, Department of Organic ChemistryDavid Milstein (Corresponding Author) - The Weizmann Institute of Science, Department of Organic Chemistry
- Resource Type
- Journal article
- Publication Details
- Journal of the American Chemical Society, Vol.140(38), pp.11931-11934; 26/Sep/2018
- Number of pages
- 4
- Language
- English
- DOI
- https://doi.org/10.1021/jacs.8b08385
- Grant note
- This research was supported by the European Research Council (ERC AdG 692775). D.M. holds the Israel Matz Professorial Chair. P.D. is thankful to the Planning and Budgeting Committee (PBC) for a postdoctoral fellowship.
- Record Identifier
- 993264870403596
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