Sustainable and selective Ni-catalyzed allylation of 2-oxindoles and 2-coumaranones in batch and flow chemistry

被引:2
|
作者
Mouhsine, Bouchaib [1 ,2 ]
Saint Pol, Anthony [1 ]
Karim, Abdallah [2 ]
Penhoat, Mael [4 ]
Dumont, Clement [1 ,3 ]
Suisse, Isabelle [1 ]
Sauthier, Mathieu [1 ]
机构
[1] Univ Lille, Univ Artois, UCCS Unite Catalyse & Chim Solide, CNRS,ENSCL,UMR 8181,Cent Lille, F-59000 Lille, France
[2] Univ Cadi Ayyad, Fac Sci Semlalia, Dept Chim, Equipe Chim Coordinat & Catalyse, BP 2390, Marrakech, Morocco
[3] ICAM, Site Lille,6 rue Auber, F-59016 Lille, France
[4] Univ Lille, USR 3290, MSAP Miniaturisat Synth Anal & Prote, F-59000 Lille, France
关键词
RADICAL-MEDIATED ALLYLATION; ASYMMETRIC-SYNTHESIS; ALPHA-ALLYLATION; ALLYLIC ALCOHOLS; DEOXYDEHYDRATION; OXINDOLES; SUBSTITUTION; NUCLEOPHILES; CYCLIZATION; ALKYLATION;
D O I
10.1039/d3re00192j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
2-Oxindoles and 2-coumaranones could be selectively allylated in the presence of low cost catalysts based on nickel, leading selectively to different polysubstituted derivatives. Allyl alcohol was used as an allylating reagent and allowed the synthesis of compounds under neutral conditions with water produced as the sole by-product. Experiments have been performed in batch and in flow chemistry. The latter protocol in flow led to a very efficient and straightforward allylic alkylation of 2-oxindoles in only a few minutes with high chemoselectivities towards either the C,C-bisallylated product or the C,C,N-trisallylated one.
引用
收藏
页码:2549 / 2556
页数:8
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