13C Chemical Shifts of Quinolizidines. 2. 13C Spectra of Some NupharAlkaloids

The 13C n.m.r. spectra of nine Nupharalkaloids: deoxynupharidine, 7-epideoxynupharidine, nupharidine, 7-epinupharidine, nupharolutine, 7-epinupharolutine, thiobinupharidine, thionu-phlutine B, and neothiobinupharidine, have been determined. Also examined were the spectra of five model compounds, 2,2,4,4-tetramethylthiolane, 3(a)-methyl-3(e)-methylthiomethylquinolizidine, 3(e)-methyl-3(a)-methylthiomethylquinolizidine, 3(e)-methylthio-3(a)-methylquinolizidine, and 3-methylfuran. This latter group of spectra were used to assist the chemical shift assignments of the Nupharalkaloids. The most significant findings of this study are: (i) axial methyl and thiomethylene groups are shielded more than their equatorial counterparts in all cases; (ii) axial and equatorial hydroxyl groups substituted at C-7 of deoxynupharidine and 7-epideoxynupharidine give α-, β-, and γ-effects in ring B similar to those in carbocyclic systems but also produce small upfield shifts in ring A especially at the carbons α to nitrogen; (iii) the effect of a 3-furyl group located at C-4 appears to have nearly the same effect on quinolizidine ring carbons as a methyl group in the same position, the effects being shielding and deshielding at the various ring carbons; (iv) N-oxide formation results in α-, β-, γ-, and δ-shielding and deshielding effects consistent with the incorporation of an axial oxygen into a trans-fused system or the formation of a cis-fused quinolizidine N-oxide; and (v) methylene or methyl groups attached to C-2 and C-4 of a thiolane, including that in the skeleton of the C30thiaspirane alkaloids, experience deshielding δ-effects.