Stereoselective synthesis of 2<i>e</i>-phenyl-4<i>e</i>-hydroxy-1-azaspiro[5.5]undecane

Authors

  • А. B. Варламов Russian People's Friendship University, Moscow 117198
  • Ф. И. Зубков Russian People's Friendship University, Moscow 117198
  • А. И. Чернышев Russian People's Friendship University, Moscow 117198
  • B. B. Кузнецов Russian People's Friendship University, Moscow 117198
  • А. Пальма Russian People's Friendship University, Moscow 117198

Abstract

6-Phenylspiro(1-aza-7-oxabicyclo[2.2.1]heptane-2-cyclohexane) was synthesized by cyclization of N-benzylidene-1-allyl-1-cyclohexylamine N-oxide, and its reduction splitting yielded 2e-phenyl-4e-hydroxy-1-azaspiro[5.5]undecane.

How to Cite
Varlamov, A. V.; Zubkov, F. I.; Chernyshev, A. I.; Kuznetcov, V. V.; Pal'ma, A. Chem. Heterocycl. Compd. 1998, 34, 69. [Khim. Geterotsikl. Soedin. 1998, 34, 77.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290615

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Published

1998-01-25

Issue

No. 1 (1998)

Section

Original Papers