Cyanide-Free Enantioselective Catalytic Strategies for the Synthesis of Chiral Nitriles

被引:22
|
作者
Groeger, Harald [1 ,2 ]
Asano, Yasuhisa [2 ]
机构
[1] Bielefeld Univ, Fac Chem, Chair Ind Organ Chem & Biotechnol, D-33615 Bielefeld, Germany
[2] Toyama Prefectural Univ, Biotechnol Res Ctr, Imizu, Toyama 9390398, Japan
来源
JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 85卷 / 10期
基金
日本学术振兴会;
关键词
SILYL KETENE IMINES; PHOSPHINE-PHOSPHITE LIGANDS; ALPHA-SUBSTITUTED NITRILES; ALDOXIME DEHYDRATASE; PHENYLACETALDOXIME DEHYDRATASE; CONJUGATE ADDITION; OXIDATIVE CLEAVAGE; ENZYMATIC METHOD; BACILLUS SP; CONSTRUCTION;
D O I
10.1021/acs.joc.9b02773
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The development of enantioselective syntheses of nitriles gained increasing interest due to, e.g., an increasing demand for chiral nitriles for drug synthesis. Complementing existing routes, recently catalytic processes enabling an enantioselective formation of the chiral nitrile moiety without the need to utilize cyanide were accomplished. It is noteworthy that these processes are complementary to each other as they are based on different types of substrates, catalytic methods (utilizing chemo- and biocatalysts), and stereochemical reaction concepts (asymmetric synthesis versus resolution).
引用
收藏
页码:6243 / 6251
页数:9
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