Academic Journal

Palladium‐Catalyzed Carbonylation of Multifunctionalized Substituted Alkynes to Quinolinone Derivatives under Mild Conditions

التفاصيل البيبلوغرافية
العنوان: Palladium‐Catalyzed Carbonylation of Multifunctionalized Substituted Alkynes to Quinolinone Derivatives under Mild Conditions
المؤلفون: Voronov, Aleksandr, Pancrazzi, Francesco, Constantin, Ana Maria, Maggi, Raimondo, Mancuso, Raffaella, Gabriele, Bartolo, Olivieri, Diego, Carfagna, Carla, Casnati, Alessandro, Rispoli, Francesco, Baldini, Laura, Ca, Nicola Della
المساهمون: Voronov, Aleksandr, Pancrazzi, Francesco, Constantin, Ana Maria, Maggi, Raimondo, Mancuso, Raffaella, Gabriele, Bartolo, Olivieri, Diego, Carfagna, Carla, Casnati, Alessandro, Rispoli, Francesco, Baldini, Laura, Ca, Nicola Della
سنة النشر: 2023
المجموعة: Università degli Studi di Urbino: CINECA IRIS
الوصف: A highly selective palladium catalyzed carbonylation of 2 alkynylanilines bearing an amide moiety to condensed six membered heterocyclic structures has been developed under mild conditions (room temperature and atmospheric pressure of CO). The carbonylative protocol is also compatible with CO surrogates, such as benzene-1,3,5-triyl triformate (TFBen) or the newly developed calix[6]arenes functionalized with six formate groups (CLX[6]CO), which are both capable to release CO in situ . A series of tricyclic fused heterocycles containing the important oxazino quinolinone scaffold have been selectively obtained ( only the 6 endo dig cyclization mode has been observed ) in good to excellent yields (up to 99%).
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:001052452400001; volume:41; issue:23; firstpage:3223; lastpage:3228; numberofpages:6; journal:CHINESE JOURNAL OF CHEMISTRY; https://hdl.handle.net/11576/2725712; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85169099862
DOI: 10.1002/cjoc.202300337
الاتاحة: https://hdl.handle.net/11576/2725712
https://doi.org/10.1002/cjoc.202300337
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.68E1198
قاعدة البيانات: BASE