## Abstract The smallest one‐bond carbon—carbon coupling constants of cyclopropane derivatives have been measured for [1‐^13^C]cyclopropane‐1,1‐dicarboxylic acid and cyclopropanecarboxylic acid. The ^13^C, ^13^C coupling constants of cyclopropylcarbinol have also been determined. The dependence of
13C NMR: The stereochemical dependence of 15N13C coupling constants in pyrazoles
✍ Scribed by T. Axenrod; P. Mangiaracina; C. M. Watnick; M. J. Wieder; S. Bulusu
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 227 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Geminal ^15^N^13^C coupling constants have been measured in a series of ^15^N‐enriched 1‒phenyl‒3,5‒dialkyl‐substituted pyrazoles. The importance of the orientation of the nitrogen lone‐pair in determining the magnitude of ^2^J(^15^N^13^C) values is reflected in the enhanced coupling observed for those carbon atoms lying close in space to the lone‐pair electrons.
📜 SIMILAR VOLUMES
## Abstract The one‐bond coupling constant ^1^__J__ ^13^CH for the halogenated carbon in α‐halogenocyclohexanones is more important when the CH bond is in the equatorial then in the axial position. When a conformational equilibrium is present, the resulting coupling is a linear function of the eq
## Abstract Two‐bond ^13^C^13^C coupling constants are discussed on the basis of INDO‐SCPT calculations. The dependence of ^2^__J__(CC) on bond angle variation and on methyl substitution is evaluated, and it is shown that ^2^__J__(CC) depends linearly on the bond orbital __s__‐character product of
## Abstract The ^15^N^13^C coupling constants in ^15^N labelled azaadamantane have been measured and interpreted in terms of their conformational dependence as compared with ^15^N‐quinuclidine.
## Abstract The dipeptide alanylproline has been prepared with the proline residue both ^13^C (15%) and ^15^N (95%) enriched. ^15^N NMR spectra of alanylproline reveal signals for both possible conformations—__cis__ and __trans__—of the dipeptide backbone in solution. Different p__K__ values for bo
## Abstract The magnitudes of ^13^C^14^N coupling constants have been measured in 12 rigid or anancomeric (biased) tetraalkylammonium iodides. The one‐bond coupling is typical for the degree of substitution of the carbon atom and the geminal coupling is very small. Vicinal couplings depend on the