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Deamination of Betti bases: a facile route to 1-alkyl-2-naphthols and phenols via a metal-free transfer hydrogenation under microwave irradiation.
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Jul2015, Vol. 56 Issue 27, p4115-4118. 4p. - Publication Year :
- 2015
-
Abstract
- A facile route to 1-alkyl-2-naphthols/phenols via deamination followed by a metal-free catalytic transfer hydrogenation of 1-(α-aminoalkyl)-2-naphthols/phenols, commonly called Betti bases under microwave irradiation has been developed. Hantzsch 1,4-dihydropyridine is used as the reductant. A mechanistic proposal involving elimination–addition mechanism is described. The reaction is simple, clean, and offers very good yields of products. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NAPHTHOL
*PHENOLS
*HYDROGENATION
*MICROWAVES
*DIHYDROPYRIDINE
*ELIMINATION reactions
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 56
- Issue :
- 27
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 103116777
- Full Text :
- https://doi.org/10.1016/j.tetlet.2015.05.031