2004Journal of Jiangxi Normal UniversityRequires access

NMR Study of Endo-8-alkoxylmethylisocamphane Derivatives

Qiuping Ding

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Abstract

The structures of 6 endo-8-alkoxylmethylisocamphane derivatives were determined by 1 D-NMR spectroscopy(~1 H NMR、~(13) C NMR、DEPT) and 2 D-NMR spectroscopy (~1 H—~1 H COSY、HSQC、HMBC、~1 H—~1 H NOESY). All the ~1 H and ~(13)C NMR data were assigned, and the varieties of chemical shifts with the substitute of the compounds were discussed. The NMR data of these compounds can be used as the reference of these series compounds.

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What this paper is about

The structures of 6 endo-8-alkoxylmethylisocamphane derivatives were determined by 1 D-NMR spectroscopy(~1 H NMR、~(13) C NMR、DEPT) and 2 D-NMR spectroscopy (~1 H—~1 H COSY、HSQC、HMBC、~1 H—~1 H NOESY). All the ~1 H and ~(13)C NMR data were assigned, and the varieties of chemical shifts with the substitute of the compounds were discussed. The NMR data of these compounds can be used as the reference of these series compounds.

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Available abstract

The structures of 6 endo-8-alkoxylmethylisocamphane derivatives were determined by 1 D-NMR spectroscopy(~1 H NMR、~(13) C NMR、DEPT) and 2 D-NMR spectroscopy (~1 H—~1 H COSY、HSQC、HMBC、~1 H—~1 H NOESY). All the ~1 H and ~(13)C NMR data were assigned, and the varieties of chemical shifts with the substitute of the compounds were discussed. The NMR data of these compounds can be used as the reference of these series compounds.

Key concepts: DEPT, Heteronuclear single quantum coherence spectroscopy, Two-dimensional nuclear magnetic resonance spectroscopy, Chemistry, Fluorine-19 NMR, Nuclear magnetic resonance spectroscopy, Carbon-13 NMR satellite, Carbon-13 NMR

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