The 'H-and "C-n.m.r. spectra of seven in&lo1 methyl ethers were recorded and assigned. They were classified into five types, and the effect of 0methyl&ion on the chemical shifts of each type is discussed. NOTE ADDED IN PROOF Type F, not encountered in our work, occurs in 1,6-anhydro-3-O-methyl-& D
Methyl substituent effects in the 13C spectra of cyclohexanone O-methyl oximes and N,N-dimethylhydrazones
✍ Scribed by Robert R. Fraser; Kasturi L. Dhawan; Kevser Taymaz
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 516 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C NMR spectra of a series of 4‐t‐butylcyclohexane‐O‐methyl oximes and N,N‐dimethylhydrazones containing α‐methyl substituents have been measured. The effects of α‐methyl substitution (syn‐axial, anti‐axial and anti‐equatorial) on the carbons α, β and γ to the substitution site are similar to those previously found in cyclohexanones. Use has been made of these substituent parameters to determine the conformational equilibria of the mobile 2‐methylcyclohexanone derivatives.
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## Abstract The complete ^1^H and ^13^C NMR spectral assignments of seven positional isomers of __N__,__N__‐dimethylsulfamoylquinolines 2–8 and quinoline have been made using 1D and 2D NMR techniques, including COSY, HMQC and HMBC experiments. Δδ~H~ and Δδ~C~ substituent effects induced by the sulf