C and in some cases also 15 N chemical shifts of quaternary benzo[c]phenanthridine alkaloids (fagaronine, chelerythrine, chelilutine, chelirubine, nitidine, sanguilutine, sanguinarine, and sanguirubine) were systematically studied by NMR spectroscopy and ab initio calculations. The assignment of sig
Piperaceae Alkaloids: Part I. Structure of piperstachine; 13C- and 1H-NMR. Studies
β Scribed by Balawant S. Joshi; Narayanan Viswanathan; Dilip H. Gawad; Wolfgang von Philipsborn
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 873 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
From the stem of Piper trichostachyon C. DC. a new alkaloid designated piperstachine (VII) has been isolated. Its structure is derived on the basis of spectral data and synthesis of hexahydropiperstachine (X).
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A detailed study of the 270 MHz IH and 67 MHz ~C NMR spectra of dimedone is reported. JcH coupling constants for the keto and enol forms are presented. In CDCI~ solution, the C-4 and C-6 carbons of the bulk polymeric enol tautomer are equivalent, with an averaged coupling to C-2, whilst they appear
The 13C NMR spectra of some 1and 2-substituted perimidines and perimidinium salts are discussed and assigned. Although the spectra of most of the 2-substituted perimidines are comparatively simple, several examples display I3C and 'H spectral characteristics indicative of inhibition of prototropic t