Reaction of trifluoroacetylchromenes with 6-aminouracils. Synthesis of pyrido[2,3-d]pyrimidines View Full Text


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Article Info

DATE

2017-04

AUTHORS

Yu. V. Popova, D. V. Osipov, V. A. Osyanin, Yu. N. Klimochkin

ABSTRACT

The condensation of trifluoroacetyl-substituted 4H-chromenes and 1H-benzo[f]chromenes with 6-amino-1,3-dimethyluracil and 6-aminothiouracil afforded a number of pyrido[2,3-d]pyrimidine derivatives containing a 2-hydroxybenzyl or 2-hydroxynaphthalen-1-ylmethyl group in the 6-position as a result of cascade transformation initiated by Michael addition.

PAGES

599-603

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428017040169

DOI

http://dx.doi.org/10.1134/s1070428017040169

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1085745580


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