A CONVENIENT ONE-POT PREPARATION OF METHYL α-ARYL β-PRIМARYLAMINO ALКANОATES

Authors

  • A. R. Katritzky Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720
  • О. Lingibe Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720
  • В. Yang Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720

Abstract

Six examples of α-aryl β-primarylamino esters (V) were synthesized by а convenient one-pot methodology, i.e. reaction of lithiated methyl α-arylacetates with 1-(triphenylphosphoranylideneaminomethyl)benzotriazole (BETMIP) followed by hydrolysis.

How to Cite
Katritzky, A. R.; Lingibe, O.; Yang, B.  Chem. Heterocycl. Compd. 1995, 31, 890. [Khim. Geterotsikl. Soedin. 1995, 1023.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01170316

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Published

1995-08-25

Issue

No. 8 (1995)

Section

Original Papers