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Saturated 5-membered ring conformations. 2—1H NMR study of protonated N-methylpyrrolidines

✍ Scribed by Y. Infarnet; J. C. Duplan; J. Huet

Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
320 KB
Volume
16
Category
Article
ISSN
0749-1581

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✦ Synopsis

Abstract

The ^1^H NMR spectra of the protonated and unprotonated forms of cis‐ and trans‐N‐methylhexahydroisoindoline, of 1,3,3,4,4‐pentamethylpyrrolidine and of 1,3,3‐trimethylpyrrolidine were analyzed. The coupling constants between the NH⊕ and the CH protons α to the nitrogen allowed the study of the conformation of the cyclic systems in pseudorotation.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v