Photodimers of 1-vinyl-2-pyridones; synthesis and study of the structure by the method of 1H and 13C NMR View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1990-07

AUTHORS

A. V. Afonin, M. A. Andriyankov, M. V. Nikitin

ABSTRACT

The action of natural light on 1-vinyl-2-pyridone and a series of its substituted compounds gave the corresponding photodimers with the retention of the vinyl group. The steric and electronic structure of the substances obtained was studied by the method of 1H and 13C NMR by comparison with the structure of the initial monomers. It was established that the stereoorientation of the vinyl group depends on the position of the substituent in the ring. More... »

PAGES

785-789

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00509708

DOI

http://dx.doi.org/10.1007/bf00509708

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1053139646


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