氰化
氢氰酸
催化作用
分子内力
腈
对映选择合成
化学
亲核加成
亲核细胞
组合化学
有机化学
作者
Nobuhito Kurono,Takeshi Ohkuma
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2015-12-28
卷期号:6 (2): 989-1023
被引量:268
标识
DOI:10.1021/acscatal.5b02184
摘要
Catalytic asymmetric cyanations of prochiral unsaturated compounds affording the corresponding nitrile products in high enantiomeric excess (≥90% in general) are summarized in this review. The nucleophilic cyanide addition onto aldehydes, ketones, and imines is promoted by chiral metal complexes and organocatalysts. Recent progress in asymmetric conjugate cyanation of α,β-unsaturated carbonyl compounds is also discussed. The asymmetric cyanation of unactivated alkenes is catalyzed by chiral transition-metal complexes. Current topics of intramolecular carbocyanation and aminocyanation in addition to the traditional hydrocyanation are reviewed.
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