Hydrogen Bonding Phase-Transfer Catalysis with Alkali Metal Fluorides and Beyond

被引:45
|
作者
Pupo, Gabriele [1 ]
Gouverneur, Veronique [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
SIGNIFICANTLY ENHANCED REACTIVITY; C-F BOND; NUCLEOPHILIC FLUORINATION; ENZYMATIC FLUORINATION; CONFORMATIONAL CONTROL; QUATERNARY AMMONIUM; KINETIC RESOLUTION; POTASSIUM FLUORIDE; ANION-BINDING; IONIC LIQUID;
D O I
10.1021/jacs.2c00190
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phase-transfer catalysis (PTC) is one of the most powerful catalytic manifolds for asymmetric synthesis. Chiral cationic or anionic PTC strategies have enabled a variety of transformations, yet studies on the use of insoluble inorganic salts as nucleophiles for the synthesis of enantioenriched molecules have remained elusive. A long-standing challenge is the development of methods for asymmetric carbon-fluorine bond formation from readily available and cost-effective alkali metal fluorides. In this Perspective, we describe how H-bond donors can provide a solution through fluoride binding. We use examples, primarily from our own research, to discuss how hydrogen bonding interactions impact fluoride reactivity and the role of H-bond donors as phase-transfer catalysts to bring solid-phase alkali metal fluorides in solution. These studies led to hydrogen bonding phase-transfer catalysis (HB-PTC), a new concept in PTC, originally crafted for alkali metal fluorides but offering opportunities beyond enantioselective fluorination. Looking ahead, the unlimited options that one can consider to diversify the H-bond donor, the inorganic salt, and the electrophile, herald a new era in phase-transfer catalysis. Whether abundant inorganic salts of lattice energy significantly higher than those studied to date could be considered as nucleophiles, e.g., CaF2, remains an open question, with solutions that may be found through synergistic PTC catalysis or beyond PTC.
引用
收藏
页码:5200 / 5213
页数:14
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