期刊
DOKLADY CHEMISTRY
卷 505, 期 2, 页码 177-183出版社
MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S0012500822700070
关键词
thiazolo[3; 2-a]pyrimidines; 2-arylmethylidene derivatives of thiazolo[3; 3; 5-diaryl-2; 3-dihydrothiazolo[3; 2-a]pyrimidine-2; 6-dicarboxylates; microwave synthesis; nucleophilic addition; intramolecular rearrangement; X-ray diffraction analysis
资金
- Kazan Scientific Center, Russian Academy of Sciences
A new method for the synthesis of 2,3-disubstituted 2,3-dihydrothiazolo[3,2-a]pyrimidines has been developed using microwave activation conditions and nucleophilic addition of methanol.
A new approach to the synthesis of 2,3-disubstituted 2,3-dihydrothiazolo[3,2-a]pyrimidines under microwave activation conditions has been developed. The method consists in the nucleophilic addition of methanol to 2-arylmethylidene derivatives of thiazolo[3,2-a]pyrimidine followed by intramolecular rearrangement to form 3,5-diaryl-2,3-dihydrothiazolo[3,2-a]pyrimidine-2,6-dicarboxylates.
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