NMR STUDY OF CONFIGURATION AND CONFORMATION OF NORBORNENE/NORBORNANE FUSED TETRACYCLIC AZETIDINONES.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

1,3- and 3. 1- structure isomers (3 or 4 and 1 or 2) of tricyclic oxazines fused with norbornene or norbornane were synthesized for pharmacological purposes. The diendo (1,3) or diexo (2,4) anellation of the heteroring to the norbornene or norbornane skeleton was confirmed by proton proton coupling data. The assignment of the proton signals were determined by double resonance experiments. The assignments of the carbon lines were proved by DEPT measurements.

Original languageEnglish
Title of host publicationUnknown Host Publication Title
PublisherUniv Zurich, Dep of Physics
Pages329-330
Number of pages2
Publication statusPublished - 1984

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Conformations
Protons
Nuclear magnetic resonance
Isomers
Carbon
Experiments

ASJC Scopus subject areas

  • Engineering(all)

Cite this

NMR STUDY OF CONFIGURATION AND CONFORMATION OF NORBORNENE/NORBORNANE FUSED TETRACYCLIC AZETIDINONES. / Sohár, P.; Stájer, G.; Bernáth, G.

Unknown Host Publication Title. Univ Zurich, Dep of Physics, 1984. p. 329-330.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

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