Aminations and arylations by direct C–O activation for the design of 7,8-dihydro-6H -5,8-ethanopyrido[3,2- d]pyrimidines
Langue
en
Article de revue
Ce document a été publié dans
RSC Advances. 2021-05-28, vol. 11, n° 32, p. 19363-19377
Royal Society of Chemistry
Résumé en anglais
The design of some novel disubstituted 7,8-dihydro-6H-5,8-ethanopyrido[3,2-d]pyrimidine derivatives is reported. The series was developed from quinuclidinone, which afforded versatile platforms bearing one lactam function ...Lire la suite >
The design of some novel disubstituted 7,8-dihydro-6H-5,8-ethanopyrido[3,2-d]pyrimidine derivatives is reported. The series was developed from quinuclidinone, which afforded versatile platforms bearing one lactam function in position C-2 that were then used to create C–N or C–C bonds for SNAr or palladium-catalyzed cross-coupling reactions by in situ C–O activation. The reaction conditions were optimized under microwave irradiation, and a wide range of amines or boronic acids were used to determine the scope and limitations of each method. To complete this study, the X-ray crystallographic data of 7,8-dihydro-6H-5,8-ethanopyrido[3,2-d]pyrimidine derivative 49 were used to formally establish the structures of the products.< Réduire
Project ANR
Synthèse Organique : des molécules au vivant - ANR-11-LABX-0029
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