Isoindolinone Synthesis: Selective Dioxane-Mediated Aerobic Oxidation of Isoindolines

التفاصيل البيبلوغرافية
العنوان: Isoindolinone Synthesis: Selective Dioxane-Mediated Aerobic Oxidation of Isoindolines
المؤلفون: Sinjinee Sardar, Esai Corral, Frank W. Foss, P. Thapa, Brad S. Pierce
المصدر: The Journal of Organic Chemistry. 84:1025-1034
بيانات النشر: American Chemical Society (ACS), 2018.
سنة النشر: 2018
مصطلحات موضوعية: inorganic chemicals, 010405 organic chemistry, Organic Chemistry, Late stage, Indoprofen, Isoindoline, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, 0104 chemical sciences, chemistry.chemical_compound, chemistry, medicine, Chemoselectivity, medicine.drug
الوصف: N-Alkyl and N-aryl-isoindolinones were prepared by a dioxane-mediated oxidation of isoindoline precursors. The transformation exhibits unique chemoselectivity for isoindonlines. A chiral tertiary (3°)-benzylic position was not racemized during oxidation, and methyl indoprofen was prepared by late stage oxidation. Mechanistic studies suggest a selective H atom transfer, which avoids many known oxidation (by-)products of isoindolinones.
تدمد: 1520-6904
0022-3263
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b104aea1bb503efae3baa6ba59ae20e2
https://doi.org/10.1021/acs.joc.8b01920
رقم الأكسشن: edsair.doi.dedup.....b104aea1bb503efae3baa6ba59ae20e2
قاعدة البيانات: OpenAIRE