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An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones. / Galenko, Ekaterina E.; Puzyk, Aleksandra M.; Novikov, Mikhail S.; Khlebnikov, Alexander F.
в: Journal of Organic Chemistry, Том 87, № 9, 06.05.2022, стр. 6459-6470.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones
AU - Galenko, Ekaterina E.
AU - Puzyk, Aleksandra M.
AU - Novikov, Mikhail S.
AU - Khlebnikov, Alexander F.
N1 - Publisher Copyright: © 2022 American Chemical Society. All rights reserved.
PY - 2022/5/6
Y1 - 2022/5/6
N2 - The synthesis of 5-aryl- and 4-aryl/hetaryl/cyclopropyl/alkynyl-5-aryl-1H-pyrrole-2,3-diones by formal isomerization of isoxazole-5-carbaldehydes mediated Mo(CO)6 in wet MeCN has been developed. The resulting 1H-pyrrole-2,3-diones are good precursors for substituted 1H-pyrrolo[2,3-b]quinoxalines.
AB - The synthesis of 5-aryl- and 4-aryl/hetaryl/cyclopropyl/alkynyl-5-aryl-1H-pyrrole-2,3-diones by formal isomerization of isoxazole-5-carbaldehydes mediated Mo(CO)6 in wet MeCN has been developed. The resulting 1H-pyrrole-2,3-diones are good precursors for substituted 1H-pyrrolo[2,3-b]quinoxalines.
UR - http://www.scopus.com/inward/record.url?scp=85128685198&partnerID=8YFLogxK
U2 - 10.1021/acs.joc.2c00386
DO - 10.1021/acs.joc.2c00386
M3 - Article
AN - SCOPUS:85128685198
VL - 87
SP - 6459
EP - 6470
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
SN - 0022-3263
IS - 9
ER -
ID: 94983185