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MOLECULAR STRUCTURE OF HETEROCYCLES. V. SOLVENT EFFECTS ON THE 17 O NMR CHEMICAL SHIFTS OF 5-TRICHLOROMETHYL-5-HYDROXY-4, 5-DIHYDROISOXAZOLES †

✍ Scribed by Martins, Marcos A. P.; Freitag, Rogério A.; Zimmermann, Nilo E.K.; Sinhorin, Adilson P.; Cúnico, Wilson; Bastos, Giovani P.; Zanatta, Nilo; Bonacorso, Helio G.


Book ID
127377212
Publisher
Taylor and Francis Group
Year
2001
Tongue
English
Weight
141 KB
Volume
34
Category
Article
ISSN
0038-7010

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13C NMR chemical shifts of heterocycles.
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## Abstract Evaluation by empirically derived equations for the substituent effect (α, β, γ, δ) on the ^13^C NMR chemical shifts for C‐3, C‐4, C‐5 and halomethyl‐substituent carbon (C‐6) in 5‐halomethyl‐5‐hydroxy‐4,5‐dihydroisoxazoles (where C‐3 substituent=H), alkyl or phenyl, C‐4 substituent=H, a