Abstract The 13 C NMR spectra of 62 oxanes (tetrahydropyrans) with and without methyl substituents at various ring positions, some of them bearing in addition (or instead) ethyl, vinyl, ethynyl, carbomethoxy and methylol substituents at C-2, have been recorded, and the 294 resulting chemical shifts have been correlated by multiple linear regression analysis. Axial and equatorial α-, β-, γ-, δ-, gem-and vic-parameters for shifts caused by methyl ...
[Smith et al. Journal of the American Chemical Society, 1951 , vol. 73, p. 5267,5269 Journal of the American Chemical Society, 1952 , vol. 74, p. 2018]