Facile One-pot Syntheses of Amidines and Enamines from Oximes via Beckmann Rearrangement Using Trifluoromethansulfonic Anhydride
- 14 February 2004
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 33 (3), 322-323
- https://doi.org/10.1246/cl.2004.322
Abstract
Facile one-pot syntheses of amidines and enamines were achieved by trapping carbocation intermediates that were formed by Beckmann rearrangement of oximes with amines and carbon nucleophiles, respectively, under mild conditions.Keywords
This publication has 15 references indexed in Scilit:
- One-Pot Synthesis of N-Imidoylbenzotriazoles via Benzotriazole-Mediated Beckmann Rearrangement of OximesOrganic Letters, 1999
- A Novel Synthesis of 1,2-Dehydro-1-aminophosphonates via Beckmann Rearrangement. Application to the Synthesis of a-Aminophosphonic Acid DerivativesHETEROCYCLES, 1997
- A new synthesis of imidoyl iodides via beckmann rearrangement of oxime sulfonatesTetrahedron Letters, 1983
- A Reinvestigation of the Reaction of Hmpa With KetoximesSynthetic Communications, 1983
- Carbon-carbon bond formation by selective coupling of enol silyl ethers with oxime sulfonatesJournal of the American Chemical Society, 1983
- Organoaluminum-promoted Beckmann rearrangement of oxime sulfonatesJournal of the American Chemical Society, 1983
- Beckman rearrangement of oxime sulfonates by grignard reagentsTetrahedron Letters, 1982
- Successive Beckmann rearrangement-alkylation sequence by organoaluminum reagents. Simple route to dl-pumiliotoxin CJournal of the American Chemical Society, 1981
- Zur Kenntniss der IsonitrosoverbindungenEuropean Journal of Inorganic Chemistry, 1887
- Zur Kenntniss der IsonitrosoverbindungenEuropean Journal of Inorganic Chemistry, 1886