SYNTHESIS AND STEREOCHEMISTRY OF (1<i>S</i>,3<i>S</i>,4<i>S</i>,7<i>R</i>,11<i>R</i>)-3-(4-NITROPHENYL)-11-AZA-2,6-DIOXATRICYCLO[5,3,1,0<sup>4,11</sup>]UNDECANE

Authors

  • Ж. Кукле Université d'Auvergne, Faculté de Farmacie, 28, Place Henri Dunant, Clermont-Ferrand
  • М. Мадесклер Universite d’Auvergne, Faculte de Farmacie 28, Place Henri Dunant, Clermont-Ferrand
  • Ф. Леаль Universite d’Auvergne, Faculte de Farmacie 28, Place Henri Dunant, Clermont-Ferrand
  • В. П. Зайцев Samara State University, Samara 443011
  • С. Х. Шарипова Samara State University, Samara 443011

Keywords:

(1S,3S,4S,7R,11R)-3-(4-nitrophenyl)-11-aza-2,6-dioxatricyclo[5,3,1,0<sup>4</sup>,11]undecane

Abstract

The reaction of (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol with glutaraldehyde has been studied. It has been established on the basis of AM1 and PM3 calculations and 1H NMR spectra recorded in the presence of the shift reagent Eu(fod)3 that (1S,3S,4S,7R,11R)-3-(4-nitrophenyl)-11-aza-2,6-dioxatricyclo[5,3,1,04,11]undecane is formed as the result of the reaction.

How to Cite
Couquelet, J.; Madesclaire, M.; Leal, F.; Zaitsev, V. P.; Sharipova, S. Kh. Chem. Heterocycl. Compd. 2001, 37, 898. [Khim. Geterotsikl. Soedin. 2001, 975.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1012463911175

Published

2001-07-25

Issue

Section

Original Papers