Configurational and conformational study of new esters derived from 2-methyl-2-azabicyclo[2.2.2]octan-5-syn(anti)-ols by NMR spectroscopy and X-ray crystallography - I

Magnetic Resonance in Chemistry

Volumn 35, Issue 12, 1997, Pages 821-828

  Fernandez M J ^a   Huertas, R ^a   Toledano, M S ^a   Galvez E ^a   Server, J ^b   Martinez Ripoll M ^b  

^a UNIVERSITY OF ALCALÁ   (Spain)

^b INSTITUTO DE QUÍMICA FÍSICA ROCASOLANO   (Spain)

Author keywords

5 syn(anti) arylcarbonyloxy 2 methyl 2 azabicyclo 2.2.2 octane; 13C NMR; 1H NMR; 1H 1H coupling constants; Conformational analysis; NMR

Indexed keywords

CONFORMATIONS; CRYSTAL STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION;

13C NMR; 1H NMR; 1H-1H COUPLING CONSTANT; 2D-NMR SPECTROSCOPY; 5-SYN(ANTI)-ARYLCARBONYLOXY-2-METHYL-2-AZABICYCLO[2.2.2]OCTANE; CONFORMATIONAL ANALYSIS; CONFORMATIONAL STUDY; COUPLING CONSTANTS; NMR-SPECTROSCOPY; SYNTHESISED;

ESTERS;

EID: 0041109282     PISSN: 07491581     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-458x(199712)35:12<821::aid-omr181>3.0.co;2-7     Document Type: Article

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