Structure elucidation and 13c NMR assignment of an 1,2,4-oxadiazole substituted pyrazole

The orientation of the substituent groups in an 1,2,4-oxadiazole substituted pyrazole, formed by reaction of a phenylnitrile oxide with an unsymmetrically substituted hydrazine is determined. One-dimensional methods as the selective INEPT and 13C1H nOe experiments are used. Both techniques provide a...

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Bibliographic Details
Main Authors: Neidlein, Richard (Author) , Kramer, Walter (Author) , Li, Sheng (Author)
Format: Article (Journal)
Language:English
Published: 1998
In: Journal of heterocyclic chemistry
Year: 1998, Volume: 35, Issue: 1, Pages: 161-163
ISSN:1943-5193
DOI:10.1002/jhet.5570350130
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/jhet.5570350130
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.5570350130
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Author Notes:Richard Neidlein, Walter Kramer, Sheng Li
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Summary:The orientation of the substituent groups in an 1,2,4-oxadiazole substituted pyrazole, formed by reaction of a phenylnitrile oxide with an unsymmetrically substituted hydrazine is determined. One-dimensional methods as the selective INEPT and 13C1H nOe experiments are used. Both techniques provide also an unambiguous assignment of the 13C nmr spectrum.
Item Description:Im Titel ist die Zahl "13" hochgestellt
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Physical Description:Online Resource
ISSN:1943-5193
DOI:10.1002/jhet.5570350130