Anhydrous organic fluoride salts and reagents prepared by a method comprising the nucleophilic Substitution of a fluorinated aromatic or fluorinated unsaturated organic compound with a salt having the formula: [QnM]x+Ax- in an inert polar, aprotic solvent; wherein M is an atom capable of supporting a formal positive charge, the n groups Q are independently varied organic moieties, n is an integer such that the [QnM] carries at least one formal positive charge, x is an integer defining the number of formal positive charge(s), +, carried by the [QnM], A- is an anionic nucleophile capable of substituting for F in the fluorinated compound and F represents fluorine or a radioisotope thereof
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
This article focuses on the development of practical approaches to the in situ generation of anhydro...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
Anhydrous organic fluoride salts and reagents prepared by a method comprising the nucleophilic Subst...
This disclosure relates to reagents and methods useful in the synthesis of aryl fluorides, for examp...
This disclosure relates to reagents and methods useful in the synthesis of aryl fluorides, for examp...
The use of low polarity aromatic solvents (benzene or toluene) and/or the removal of inorganic salts...
The original specific aims of the grant where cut back considerably as the study section reduced bot...
Methods for the fluorination of organoboron compounds are described. This review will cover the fluo...
The use of low polarity aromatic solvents (benzene or toluene) and/or the removal of inorganic salts...
Solution phase reactivity of nucleophilic fluoride reagents is attenuated by ion-pairing interaction...
Methods for the fluorination of organoboron compounds are described. This review will cover the fluo...
Fluoride ion sources have been surveyed and perfluoroalkyl anions and hindered amine/HF adducts prep...
A new organocatalyzed fluoride metathesis reaction between fluoroarenes and carbonyl derivatives is ...
Nucleophilic ionic sources of fluoride are essential reagents in the synthetic toolbox to access hig...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
This article focuses on the development of practical approaches to the in situ generation of anhydro...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
Anhydrous organic fluoride salts and reagents prepared by a method comprising the nucleophilic Subst...
This disclosure relates to reagents and methods useful in the synthesis of aryl fluorides, for examp...
This disclosure relates to reagents and methods useful in the synthesis of aryl fluorides, for examp...
The use of low polarity aromatic solvents (benzene or toluene) and/or the removal of inorganic salts...
The original specific aims of the grant where cut back considerably as the study section reduced bot...
Methods for the fluorination of organoboron compounds are described. This review will cover the fluo...
The use of low polarity aromatic solvents (benzene or toluene) and/or the removal of inorganic salts...
Solution phase reactivity of nucleophilic fluoride reagents is attenuated by ion-pairing interaction...
Methods for the fluorination of organoboron compounds are described. This review will cover the fluo...
Fluoride ion sources have been surveyed and perfluoroalkyl anions and hindered amine/HF adducts prep...
A new organocatalyzed fluoride metathesis reaction between fluoroarenes and carbonyl derivatives is ...
Nucleophilic ionic sources of fluoride are essential reagents in the synthetic toolbox to access hig...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
This article focuses on the development of practical approaches to the in situ generation of anhydro...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...