## Abstract The ^13^C NMR spectra of all azabenzenoid isoxazolopyridines and some of their chloro derivatives are discussed. All ^13^C resonances were unambiguously assigned by means of gated decoupled spectra, from which one‐bond and long‐range ^13^C^1^H coupling constants have been determined fr
Carbon-13 NMR study of 5-triphenyl-phosphoranilydeneaminopyrazoles
✍ Scribed by Antonio Arques; Pedro Molina; María Victoria Vinader; José Elguero
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 258 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^13^C chemical shifts and ^13^C–^31^P coupling constants are reported for nineteen pyrazoles bearing an NPPh~3~ substituent at position 5. The three heterocyclic carbons are coupled with the phosphorus (^2^J, ^3^J and ^4^J). These couplings are very sensitive to the nature of the subtituent at position 4 [CHO, CHCHCOMe, CH(CH~2~NO~2~)~2~, CHNR, CH~2~NHR and CH~2~N(COR)Ar].
📜 SIMILAR VOLUMES
13CNMR chemical shifts of 23 aniline and 1.8diaminonaphthalene derivatives are reported; the parent compounds are also included for purposes of comparison.
## Abstract The carbon‐13 NMR spectra of a series of __exo__‐and __endo__‐epimers of 2‐substituted benzonorbornene (2‐substituent = OH, OCHO, Br, NH~2~, NHMe or NMe~2~) have been examined. The spectra are readily assigned by comparison with the coupled and off‐resonance proton decoupled spectra as