Pd-Catalyzed Switchable Access to Imines and Amines from Secondary Alcohols

被引:3
|
作者
Raydan, Daniel [1 ,2 ]
Royo, Beatriz [2 ]
Marques, M. Manuel B. [1 ]
机构
[1] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, LAQV REQUIMTE, Campus Caparica, P-2829516 Caparica, Portugal
[2] Univ Nova Lisboa, ITQB NOVA, Inst Tecnol Quim & Biol Antonio Xavier, Ave Republ, P-2780157 Oeiras, Portugal
关键词
Amine; Catalysis; Imine; Indole; Palladium; N-ALKYLATION; HYDROAMINATION; AMINATION; TERTIARY; HYDROGEN; HYDROAMINOMETHYLATION; DEHYDROGENATION; DEHYDRATION; CONVERSION; AMIDES;
D O I
10.1002/ajoc.202300282
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The use of Pd(OAc)(2) as catalyst for the challenging synthesis of imines through acceptorless alcohol dehydrogenation using secondary alcohols and amines is reported. The reaction requires low catalyst loading, shows high selectivity for the formation of the imine without the need of adding any base or additive, and can be scaled up. Interestingly, when the catalytic reaction is performed in a closed system, in the presence of base, the reaction selectively yields the corresponding amine. To highlight the practical utility of the synthesis of imines, a family of structurally important scaffold, an indole, were synthesized.
引用
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页数:4
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