Reactions of Amidines with 5-Methylene-1,3-dioxolan-2-ones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2004-08

AUTHORS

A. A. Bogolyubov, N. B. Chernysheva, V. V. Nesterov, M. Yu. Antipin, V. V. Semenov

ABSTRACT

The composition and yields of the products from the reaction of 4,4-dialkyl-5-methylene-1,3-dioxolan-2-ones with amidines depend on the structure of the initial amidine and on the reaction conditions. 2-Aminopyridines lead to 3-substituted 4-hydroxy-4-methyloxazolidin-2-ones and 4-methylene-oxazolidin-2-ones and also to sym-carbamides. 2-Amino-4,6-dimethylpyrimidine leads to the corresponding 4-methyleneoxazolidin-2-one. 3-Aminothiazoles give linear oxourethanes and sym-carbamides.

PAGES

992-1001

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/b:cohc.0000046687.48079.62

DOI

http://dx.doi.org/10.1023/b:cohc.0000046687.48079.62

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014377993


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