Synthesis and 1H and 13C NMR study of th
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V. Vijayabaskar; S. Perumal; S. Selvaraj; M. J. E. Hewlins
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Article
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1999
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John Wiley and Sons
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English
⚖ 113 KB
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The reaction of 2,6-diarylidenecyclohexanones with hydrazine hydrate in glacial acetic acid resulted in the formation of diastereomers of (E)-2-acetyl-3-aryl-7-arylidene-3,3a,4,5,6,7-hexahydroindazoles. The relative conÐgurations of these diastereomers were unambiguously assigned using 1H and 13C NM