http://www.cnr.it/ontology/cnr/individuo/prodotto/ID199488
The Rabe amination after a century: direct addition of N-heterocycles to carbonyl compounds (Articolo in rivista)
- Type
- Label
- The Rabe amination after a century: direct addition of N-heterocycles to carbonyl compounds (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/ c2ob25595b (literal)
- Alternative label
D. M. Scarpino Schietroma, M. R. Monaco, V. Bucalossi, P. E. Walter, P. Gentili, M. Bella (2012)
The Rabe amination after a century: direct addition of N-heterocycles to carbonyl compounds
in Organic & biomolecular chemistry; The Royal Society of Chemistry, Cambridge (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- D. M. Scarpino Schietroma, M. R. Monaco, V. Bucalossi, P. E. Walter, P. Gentili, M. Bella (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
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- Note
- ISI Web of Science (WOS) (literal)
- Scopus (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Chimica e IMC-CNR - Sezione Meccanismi di Rezione \"Sapienza\" Università di Roma, P.le Aldo Moro 5, 00185 Roma, Italy (literal)
- Titolo
- The Rabe amination after a century: direct addition of N-heterocycles to carbonyl compounds (literal)
- Abstract
- A catalytic version of the Rabe electrophilic amination is presented.
This kind of reaction was originally employed in 1918
in a key step for the conversion of quinotoxine to quinine.
Ketones and ?-substituted aldehydes give the corresponding
?-aminated carbonyl compounds in moderate yield. ?,?-
Unsubstituted aldehydes give rise to amino ketones via a
novel rearrangement. (literal)
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