Reduction with N-benzyl-1,4 dihydronicotinamide. A reinvestigation. |
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| Affiliation: | 1. Institut de Chimie des Milieux et Matériaux de Poitiers, UMR CNRS 7285, 4 rue Michel Brunet, B28, 86000 Poitiers, France;2. Inserm, UMR 892, CNRS, UMR 6299, University of Nantes, 8 quai Moucousu, 44007 Nantes cedex 1, France;3. Réseau Epigénétique du Cancéropôle Grand Ouest, France;4. Institut de chimie, UMR CNRS 7272, UNSA, F-06108 Nice, France;5. School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, 30 Quai Ernest-Ansermet, 1211 Geneva, Switzerland;1. Università degli Studi di Firenze, NEUROFARBA Dept., Sezione di Scienze Farmaceutiche, Via Ugo Schiff 6, 50019 Sesto Fiorentino (Florence), Italy;2. Università degli Studi di Firenze, Polo Scientifico, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy;1. al-Farabi Kazakh National University, Center of Physical Chemical Methods of Research and Analysis, Almaty, Kazakhstan;2. Iowa State University, Department of Agricultural and Biosystems Engineering, Ames, IA, USA |
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| Abstract: | 
3- or 4-Formylpyridines, cyclohexen -2 one andg-nitrostyrene can be reduced with BNAH: these substrates were previously reported to be inert or very unreactive toward this reagent. |
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