Lossen rearrangement by Rh(iii)-catalyzed C–H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives

التفاصيل البيبلوغرافية
العنوان: Lossen rearrangement by Rh(iii)-catalyzed C–H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives
المؤلفون: Dmitry A. Petropavlovskikh, Oleg A. Filippov, Sergey E. Nefedov, Daria V. Vorobyeva, Ivan A. Godovikov, Sergey N. Osipov
المصدر: Organic & Biomolecular Chemistry. 19:9421-9426
بيانات النشر: Royal Society of Chemistry (RSC), 2021.
سنة النشر: 2021
مصطلحات موضوعية: chemistry.chemical_classification, Annulation, Chemistry, Aryl, Organic Chemistry, Triple bond, Biochemistry, Medicinal chemistry, Amino acid, Catalysis, chemistry.chemical_compound, Lossen rearrangement, Moiety, Organic synthesis, Physical and Theoretical Chemistry
الوصف: A convenient and robust method for the preparation of new CF3-containing 2-quinolones has been developed via a Rh(III)-catalyzed C–H activation/Lossen rearrangement/annulation cascade of N-pivaloyloxy-arylamides with internal alkynes bearing an α-CF3-α-amino acid moiety on the triple bond. This work expands the scope of valuable products that are available through C–H activation/annulation reactions of arylamides in organic synthesis.
تدمد: 1477-0539
1477-0520
DOI: 10.1039/d1ob01711j
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6977f621392a0fe05d44b1eb07492035
https://doi.org/10.1039/d1ob01711j
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....6977f621392a0fe05d44b1eb07492035
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14770539
14770520
DOI:10.1039/d1ob01711j