Ru(II)-Catalyzed C–H Aminocarbonylation of N-(Hetero)aryl-7-azaindoles with Isocyanates

التفاصيل البيبلوغرافية
العنوان: Ru(II)-Catalyzed C–H Aminocarbonylation of N-(Hetero)aryl-7-azaindoles with Isocyanates
المؤلفون: Jeong, Taejoo, Lee, Suk Hun, Chun, Rina, Han, Sangil, Han, Sang Hoon, Jeon, Yeong Uk, Park, Jihye, Yoshimitsu, Takehiko, Mishra, Neeraj Kumar, Kim, In Su
المصدر: The Journal of Organic Chemistry; 20240101, Issue: Preprints
مستخلص: The ruthenium(II)-catalyzed C–H aminocarbonylation of N-(hetero)aryl-7-azaindoles with isocyanates is described. The excellent site selectivity at the ortho-position within the N-(hetero)aryl ring was observed to provide ortho-amidated N-(hetero)aryl-7-azaindoles under the mild reaction conditions. The resulting 7-azaindole derivatives can be readily transformed into 7-azaindoles containing carboxylic acid and alkyl amine functional groups.
قاعدة البيانات: Supplemental Index
الوصف
تدمد:00223263
DOI:10.1021/acs.joc.8b00388