Cu-Catalyzed Intramolecular Borylation-Cross Coupling Reaction of Unactivated Alkenes to Borylated Indolines

被引:1
|
作者
Fan, Lin [1 ]
Yan, Xinlong [1 ]
Li, Changjiang [1 ]
Cao, Yuxue [1 ]
Liu, Guodu [1 ]
机构
[1] Inner Mongolia Univ, Coll Chem & Chem Engn, Inner Mongolia Key Lab Fine Organ Synth, 235 Daxue West Rd, Hohhot 010021, Peoples R China
基金
中国国家自然科学基金;
关键词
Intramolecular Borylation-Cross Coupling Reaction; Copper; 3-Substituted Borylated Indolines; Unactivated Alkenes; B(2)pin(2); ENANTIOSELECTIVE HYDROBORATION; CARBONYL-COMPOUNDS; DERIVATIVES; BIS(PINACOLATO)DIBORON; ELECTROPHILES; ARYLBORATION; PALLADIUM; SECONDARY; ALKYNES; ESTERS;
D O I
10.1002/adsc.202300888
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cu-catalyzed intramolecular borylation-cross coupling reaction of alkenes was developed. Racemic and chiral borylated indolines were achieved by borylation-cross coupling of alkenes with B2pin2 via simultaneous construction of C-C and C-B bonds by Cu/phosphine ligand system. With CuOAc and DPPE ligand, a series of 3-substituted borylated indoline derivatives were concisely synthesized in good to excellent yields in short time under mild conditions. Asymmetric synthesis was investigated by ligand screening, and the chiral 3-substituted borylated indoline was obtained in 80% yield and 80:20 er with (R, R)-Me-Duphos. Application of 3-substituted borylated indolines has been demonstrated by a gram scale synthesis and further functionalization.
引用
收藏
页码:4227 / 4232
页数:6
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