scholarly journals PHASE EQUILIBRIA IN THE CONDENSED SYSTEM BROMINE TRIFLUORIDE-URANIUM HEXAFLUORIDE

1953 ◽  
Author(s):  
J Fischer ◽  
R C Voge
Keyword(s):  
Phase Equilibria ◽  
Condensed System ◽  
Uranium Hexafluoride ◽  
Bromine Trifluoride

scholarly journals Phase Equilibria in the Condensed System Bromine-Bromine Trifluoride

1954 ◽  
Vol 76 (6) ◽  
pp. 1497-1498 ◽  
Author(s):  
Jack Fischer ◽  
Robert K. Steunenberg ◽  
Richard C. Vogel
Keyword(s):  
Phase Equilibria ◽  
Condensed System ◽  
Bromine Trifluoride

Phase equilibria in the condensed system n-docosane–cyclododecane–n-decane

2016 ◽  
Vol 90 (7) ◽  
pp. 1498-1500 ◽  
Author(s):  
A. A. Shamitov ◽  
I. K. Garkushin ◽  
A. V. Kolyado
Keyword(s):  
Phase Equilibria ◽  
Condensed System

The Condensed System Bromine Trifluoride-Antimony Pentafluoride

1955 ◽  
Vol 77 (22) ◽  
pp. 5848-5849 ◽  
Author(s):  
J. Fischer ◽  
R. Liimatainen ◽  
J. Bingle
Keyword(s):  
Condensed System ◽  
Antimony Pentafluoride ◽  
Bromine Trifluoride

Recent Advances in the Synthesis of Acyl Fluorides

Synthesis ◽  
2020 ◽  
Author(s):  
Marie Gonay ◽  
Chloé Batisse ◽  
Jean-François Paquin
Keyword(s):  
Transition Metal ◽  
Organic Synthesis ◽  
Peptide Synthesis ◽  
Uranium Hexafluoride ◽  
Metal Catalysts ◽  
Recent Advances ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed ◽  
Nucleophilic Fluorination ◽  
Bromine Trifluoride

AbstractAcyl fluorides are valuable intermediates in organic synthesis. They are increasingly employed in peptide synthesis, in challenging esterification and amidation reactions or in transition-metal-catalyzed transformations. This review summarizes recent advances in their preparation.1 Introduction2 Nucleophilic Fluorination2.1 α-Fluoroamine Reagents2.2 Sulfur-Based Reagents2.3 Metal Catalysts2.4 Phosphorus-Based Reagents2.5 N,N′-Dicyclohexylcarbodiimide/HF·Pyridine2.6 Uranium Hexafluoride2.7 Bromine Trifluoride3 Radical Fluorination4 Conclusion

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