3 a ) and (3c) or (Sf) formed as minor products on reaction ( I ) with methyl acryiate or methyl propiolate were synthesized isomer-free from the diester (1') and characterized. The data for the compounds prepared are summarized in Table .
Comparative conformational studies of cyclic derivatives by 13C NMR spectroscopy
✍ Scribed by Joseph Casanova; Jean-Pierre Zahra; Bernard Waegell
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 315 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^13^C chemical shift of the substituted or functionalized carbon of various medium and large rings is plotted against ring size (6–15 carbons). The curves thus obtained allow a conformational analysis of the corresponding derivatives.
📜 SIMILAR VOLUMES
## Abstract The conformational equilibrium constants for isomeric methylcyclohexanols (__cis__‐ and __trans__‐1,2‐, 1,3‐ and 1,4‐methylcyclohexanols) have been determined from peak area measurements in the completely proton decoupled low temperature ^13^C NMR spectra of the individual conformers. T
## Abstract The ^13^C and ^1^H NMR spectra of a series of methiodides of mono‐ and di‐C‐methyl derivatives of 1‐methyl‐4‐phenyl‐4‐piperidinols are reported and chemical shift data analysed in terms of configurations and conformations of isomeric sets. Results demondtrate the value of quaternary sal
## Abstract The carbon‐13 spectra of seventeen bicyclo[3.1.1]‐heptane derivatives have been recorded and assigned. Study of the C‐6 and C‐7 chemical shifts permits the conformations to be assigned to the bridged chair, Y‐shaped, or bridged boat conformations. The spectrum of verbenone is anomalous
## Abstract Vicinal and geminal ^13^CO~2~H^1^H coupling constants are reported for malic and thiomalic acids at various pH values and related, in a comparative manner, to the known conformational information obtained by ^1^H NMR.