## Abstract A relatively fast rotation around the α,β carbon–carbon double bond at the equilibrium of geometrical isomers and a comparatively slow rotation around the carbon‐nitrogen single bond in compounds of the type (X~1~, X~2~ are electron‐attracting substituents) were detected and investiga
Dynamic NMR study of hindered rotation around the CN bond in thiopiperidides
✍ Scribed by Mariana Ciureanu; Victor E. Sahini; Felicia Cornea; Cornelia Cercasov; Mihai Contineanu
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 356 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The barriers to internal rotation about the CN bond in several thiopiperidides have been determined by the NMR technique. It was found that the barrier height (Δ__G__^‡^) increases in the series cinnamoylthiopiperididem‐and p‐substituted cinnamoylthiopiperidides the barriers were shown to increase with the electron withdrawing character of the substituent in the aromatic ring.
📜 SIMILAR VOLUMES
## Abstract Rapid __Z__,__E__‐isomerization of nitroenamines RNHCHC(NO~2~)COOCH~3~ in solutions was investigated by dynamic NMR spectroscopy. In weakly basic solvents all the studied nitroenamines isomerize by a thermal mechanism. In pyridine the isomerization proceeds by the thermal mechanism i
## Abstract Herein, a series of separate dynamic ^1^H NMR effects are reported at different temperatures within a particular enaminoester involving a phenanthridine. These effects are attributed to restricted rotation around the two single bonds such as carbon–carbon (H~a~CCH~b~) and nitrogen–car
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