Synthesis, stereochemistry, and isomeric transformations of 4-aryl-5-aroyl-2-methylthio-2-imidazolines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1988-11

AUTHORS

V. A. Konovalov, O. N. Bubel', I. G. Tishchenko

ABSTRACT

The corresponding 4-aryl-5-aroyl-2-methylthio-2-imidazolines were obtained by the reaction of complexes of cis- and trans-3-aroylaziridines and boron trifluoride with methyl thiocyanate. It is shown on the basis of spectral data that the aziridine ring is opened regiospecifically at the C(2) atom and stereospecifically with inversion of the configuration.

PAGES

1229-1233

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00633501

DOI

http://dx.doi.org/10.1007/bf00633501

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1041521394


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