Abstract
Six examples of α-aryl-β primarylamino esters (V) were synthesized by a convenient one pot methodology, i.e., reaction of lithiated methyl α-aryl-acetates with 1-(triphenylphosphoroylideneaminomethyl)benzotriazole (BETMIP) followed by hydrolysis.
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Additional information
Submitted in honor of the 60th anniversary of Professor Nikolai S. Zefirov, an outstanding Russian chemist and a good friend. by Alan R. Katritzky.
Center for Heterocyclic Compounds, Department of Chemistry, University of Flo rida, Gainesville, Florida 32611–7200, USA. Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1023–1025, August, 1995. Original article submitted July 3, 1995.
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Katritzky, A.R., Lingibe, O. & Yang, B. A convenient one-pot preparation of methylα-aryl-β-primarylamino alkanoates. Chem Heterocycl Compd 31, 890–892 (1995). https://doi.org/10.1007/BF01170316
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DOI: https://doi.org/10.1007/BF01170316