Pyridofuroxan ([1,2,5]oxodiazolo [3,4-b]pyridine 1-oxide) undergoes isomerization between the N1oxide and N3-oxide forms which can be observed by the 1 H, 13 C and 15 N NMR spectroscopy but not by 14 N and 17 O NMR at ambient and low temperatures. The rearrangement becomes slower at low temperatures
Stereochemical arrangement of spiro[4.5]decane derivatives by 15N and 17O NMR spectroscopy
✍ Scribed by Armando Ariza-Castolo; Joseantonio Godoy-Reyes
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 104 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The relative axialÈequatorial position of spiro[4.5]decanes substituted in the 1,4-positions by oxygen or nitrogen were assigned by 15N and 17O NMR spectroscopy. The substituent, chemical exchange and steric e †ects upon the chemical shifts are discussed. A linear relationship between 15N and 17O was found and the relative conÐguration of the chiral spiro atom was determined.
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