![Diastereoselective synthesis of chromeno[4,3-d]pyrimidines](/upload/12631c5e396938a702bdd516ae8c4208/issues/cover/aeeadbe79f068d9885fba8f04ac27a3b.png)
аспирант с 01.01.2023 по настоящее время
Ярославский государственный технический университет
студент с 01.01.2018 по 01.01.2023
Ярославль, Ярославская область, Россия
аспирант
Ярославль, Ярославская область, Россия
Ярославль, Ярославская область, Россия
УДК 547.853.3 Пиримидин
The paper investigates the diastereoselective synthesis of chromeno[4,3-d]pyrimidines by isolation and cyclization of diastereomerically pure dihydropyrimidine addition intermediates to resorcinol. The authors discovered the reversibility of the addition reaction to be an important factor that could neutralize the dominant formation of one of the intermediate diastereomers.
hexahydrochromeno[4,3-d]pyrimidines, resorcinol, acid-catalyzed condensation, diastereoselectivity
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