化学
立体中心
氟
催化作用
分子
碳纤维
方位(导航)
中心(范畴论)
纳米技术
对映选择合成
立体化学
有机化学
结晶学
复合数
复合材料
地图学
材料科学
地理
作者
Subarna Jyoti Kalita,Jing Qi,Lu Xiao,Debarshi Saha,Yiyong Huang,Norio Shibata
标识
DOI:10.1021/acs.chemrev.5c00177
摘要
Fluorine, due to its unique ability to modify the physicochemical and biological properties of parent molecules, has found wide applications as pharmacological modulators in drug development research. Consequently, the portion of fluorine-containing drugs has increased to about 20% in recent years. Among these, fluorine-containing drugs with aromatic fluoro-substitutions are more common than those with fluoro-substitutions at stereogenic centers. In fact, in the past decade, out of 116 fluorine-containing drugs approved by the FDA only 16 drugs are enantiomerically pure, featuring fluorine-containing stereogenic carbon centers. Asymmetric induction during building these drug molecules is largely achieved through either the "chiral pool" or "chiral resolution" approach, while the "asymmetric catalysis" approach remains underexplored. In order to draw the attention of the scientific community to this disparity, this review highlights the innovations (2015-2024) in asymmetric methodologies for creating molecules bearing a fluorine-containing stereogenic carbon center in the presence of organo- or organometallic catalysts. The synthetic strategies are divided into two sections based on fluorine-containing building blocks and fluorine-containing reagents, which are further classified by the reaction types. Special attention has been paid to synthetic challenges, types of substrates, products and catalysts, functional group compatibility, transition states, mechanistic insights, as well as synthetic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI