Preparative-Scale Synthesis of Vedejs']js Chiral DMAP Catalysts

被引:8
|
作者
Kinens, Artis [1 ,2 ]
Balkaitis, Simonas [1 ,2 ]
Suna, Edgars [1 ,2 ]
机构
[1] Latvian Inst Organ Synth, Aizkraukles 21, LV-1006 Riga, Latvia
[2] Univ Latvia, Dept Chem, Jelgavas 1, LV-1004 Riga, Latvia
来源
JOURNAL OF ORGANIC CHEMISTRY | 2018年 / 83卷 / 20期
关键词
KINETIC RESOLUTION; ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC ACYLATION; SEC-ALCOHOLS; DERIVATIVES; 4-(DIMETHYLAMINO)PYRIDINE; LITHIATION; COMPLEXES; AMINATION; AROMATICS;
D O I
10.1021/acs.joc.8b01687
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A scalable synthesis of chiral Vedejs-type DMAP catalysts is reported. The key step of the synthesis is amination of the enantiomerically pure 4-chloropyridine derivative using well-defined ZnCl2(amine)(2) complexes. A series of Zn(II)-amine complexes have been synthesized to explore the scope of the ZnCl2-mediated amination of 4-halopyridines. Mechanistic studies support a Zn(II)-facilitated nucleophilic aromatic substitution as a plausible mechanism for the chlorine-to-amine exchange.
引用
收藏
页码:12449 / 12459
页数:11
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