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Kondrat'eva, G. Ya., Medvedskaya, L. B., Ivanova, Z. N. (1971) Reaction of oxazoles with the methyl ester of acetylenedicarboxylic acid. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 2148-2150 doi:10.1007/bf00851268

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Reference TypeJournal (article/letter/editorial)
TitleReaction of oxazoles with the methyl ester of acetylenedicarboxylic acid
JournalBulletin of the Academy of Sciences of the USSR Division of Chemical Science
AuthorsKondrat'eva, G. Ya.Author
Medvedskaya, L. B.Author
Ivanova, Z. N.Author
Year1971 (October)Volume20
PublisherSpringer Science and Business Media LLC
DOIdoi:10.1007/bf00851268Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID4276987Long-form Identifiermindat:1:5:4276987:9
GUID0
Full ReferenceKondrat'eva, G. Ya., Medvedskaya, L. B., Ivanova, Z. N. (1971) Reaction of oxazoles with the methyl ester of acetylenedicarboxylic acid. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 2148-2150 doi:10.1007/bf00851268
Plain TextKondrat'eva, G. Ya., Medvedskaya, L. B., Ivanova, Z. N. (1971) Reaction of oxazoles with the methyl ester of acetylenedicarboxylic acid. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 2148-2150 doi:10.1007/bf00851268
In(1971) Bulletin of the Academy of Sciences of the USSR Division of Chemical Science Vol. 20. Springer Science and Business Media LLC

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Kondrat'eva, G. Ya., Medvedskaya, L. B., Ivanova, Z. N., Shmelev, L. V. (1971) Reaction of oxazoles with acetylenic aldehydes and ketones. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 1278 doi:10.1007/bf00855410
Kondrat'eva, G. Ya., Medvedskaya, L. B., Ivanova, Z. N. (1972) Reaction of oxazoles with dienophiles of the methylenemalonic ester type. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 21. 2072 doi:10.1007/bf00854653
Medvedskaya, L. B., Kondrat'eva, G. Ya., Bykanova, N. V. (1979) 2-alkyl-substituted oxazoles in reaction with acetylenedicarboxylic ester. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 28. 1490-1492 doi:10.1007/bf00947329
Medvedskaya, L. B., Makarov, M. G., Kondrat'eva, G. Ya. (1973) Structural direction of the heterodiene synthesis in the reaction of oxazoles with acetylenic dienophiles. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 22. 1267-1270 doi:10.1007/bf00928602
MEDVEDSKAYA, L. B., KONDRAT'EVA, G. YA., BYKANOVA, N. V. (1980) ChemInform Abstract: 2-ALKYL-SUBSTITUTED OXAZOLES IN A REACTION WITH ACETYLENEDICARBOXYLIC ACID ESTER. Chemischer Informationsdienst, 11 (15) doi:10.1002/chin.198015254
Kondrat'eva, G. Ya., Aitzhanova, M. A., Bogdanov, V. S., Ivanova, Z. N. (1978) Synthesis of 5-R2 N-oxazoles from ?-N-acylated amino acids. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 27. 773-777 doi:10.1007/bf00925305
Kondrat'eva, G. Ya., Aitzhanova, M. A., Bogdanov, V. S., Ivanova, Z. N. (1978) Reaction of N-acylated ?-amino acids with primary amines. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 27. 963-969 doi:10.1007/bf00929001
Kondrat'eva, G. Ya., Bogdanov, V. S., Ivanova, Z. N., Aitzhanova, M. A. (1977) Noncyclic dimer of 4-methyl-2-dimethylaminooxazole. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 26. 1552-1553 doi:10.1007/bf00928561
Eidus, Ya. T., Lebedev, B. L., Korytina, O. A. (1971) Transformations of methyl ester of cyclohexanecarboxylic acid in the presence of Co-kieselguhr catalyst. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 787-789 doi:10.1007/bf00853928
Komarov, N. V., Yarosh, O. G., Ivanova, Z. G. (1971) Preparation of organoalkoxysillacetylenes. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 20. 790-791 doi:10.1007/bf00853929
Nesterov, L. V., Sabirova, R. A. (1975) Reaction of methyl ester of n-methylimidoacetic acid with chloral. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 24. 898 doi:10.1007/bf00920728
 
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