## Abstract The ^1^H NMR spectra of isomeric 5,6βdimethylβ2βoxoβ1,4βdioxans have been recorded and the pertinent chemical shifts and coupling constants determined. The parameters indicate that both isomers exist as an equilibrium mixture of interconverting half chair ring conformations.
1H NMR spectra of cis-2,6-diphenylpiperidines and cis-2,6-diphenyl-4-piperidones
β Scribed by N. Arumugam; M. Sundharavadivelu; S. Sivasubramanian; D. A. Wilson
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 231 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
H NMR spectra of t-3-ethyl-r-2,~-6-diphenylpiperidine, t-3-ethyl-r-2,~-6-dipheny1-4-piperidone and several related compounds have been obtained in deuteriochloroform and deuteriotrifluoroacetic acid solutions, and compared with the spectra of their hydrochlorides in deuteriochloroform-hexadeuteriodimethy! sulphoxide solutions. The effects of the structural changes 4-CH2 -+ 4-C=0, =NH -+ =NMe and fN: -+ z N H ( 2 h D ) have been observed on the chemical shifts of ring and substituent protons, and on the non-equivalence of the diastereotopic protons of the ethyl groups.
π SIMILAR VOLUMES
Extraction with ethyl acetate or ether and distillation of the crude furnishes pure (2). As shown in the reaction scheme, the overall reaction proceeds via several unisolated intermediates and it has not yet been established whether the cyclization occurs with (la) or ( 1 b). Remarkably, in the pres