The Mannich reaction of hydrazones: improved reactivity under solvent-free conditions
暂无分享,去创建一个
[1] L. Grimaud,et al. Studies towards the synthesis of Fipronil® analogues: improved decarboxylation of α-hydrazonoacid derivatives , 2002 .
[2] V. Pecharsky,et al. Solvent-free mechanochemical synthesis of phosphonium salts. , 2002, Chemical communications.
[3] A. Majee,et al. The Mannich Reaction of Hydrazones Amenable to Solid Phase Synthesis: A Powerful Tool for Heterocycle Preparation , 2002 .
[4] Chao‐Jun Li,et al. Highly efficient Grignard-type imine additions via C-H activation in water and under solvent-free conditions. , 2002, Chemical communications.
[5] Jieyu Hu,et al. Discovery of exceptionally efficient catalysts for solvent-free enantioselective hetero-Diels-Alder reaction. , 2002, Journal of the American Chemical Society.
[6] G. Sankar,et al. Solvent-free routes to clean technology. , 2001, Chemistry.
[7] A. Mazzanti,et al. Solvent-free asymmetric aminoalkylation of electron-rich aromatic compounds: stereoselective synthesis of aminoalkylnaphthols by crystallization-induced asymmetric transformation. , 2001, The Journal of organic chemistry.
[8] J. Elguero,et al. Solvent-free preparation of tris-pyrazolyl-1,3,5-triazines , 2001 .
[9] A. Majee,et al. The use of hydrazones for efficient mannich type coupling with aldehydes and secondary amines , 2000 .
[10] W. Ried,et al. Beiträge Zur Mannich‐Reaktion , 1957 .
[11] G. Pulvermacher. Ueber Homo‐o‐phtalimid , 1887 .