γ-Valerolactone as a Renewable Dipolar Aprotic Solvent Deriving from Biomass Degradation for the Hiyama Reaction

2014 ◽  
Vol 2 (10) ◽  
pp. 2461-2464 ◽  
Author(s):  
Ermal Ismalaj ◽  
Giacomo Strappaveccia ◽  
Eleonora Ballerini ◽  
Fausto Elisei ◽  
Oriana Piermatti ◽  
...  
Keyword(s):  
Aprotic Solvent ◽  
Biomass Degradation ◽  
Dipolar Aprotic Solvent

scholarly journals Butadiene sulfone as ‘volatile’, recyclable dipolar, aprotic solvent for conducting substitution and cycloaddition reactions

2015 ◽  
Vol 3 (1) ◽  
Author(s):  
Yong Huang ◽  
Esteban E. Ureña-Benavides ◽  
Afrah J. Boigny ◽  
Zachary S. Campbell ◽  
Fiaz S. Mohammed ◽  
...  
Keyword(s):  
Aprotic Solvent ◽  
Cycloaddition Reactions ◽  
Dipolar Aprotic Solvent

ChemInform Abstract: AROMATIC NUCLEOPHILIC EXCHANGE REACTIONS PART 3, DIPOLAR APROTIC SOLVENT EFFECTS

1973 ◽  
Vol 4 (30) ◽  
pp. no-no
Author(s):  
BRIAN DACRE ◽  
DAVID F. MAUNDRELL ◽  
SUSAN E. REES
Keyword(s):  
Solvent Effects ◽  
Aprotic Solvent ◽  
Exchange Reactions ◽  
Dipolar Aprotic Solvent ◽  
Nucleophilic Exchange

Liquid Ammonia as a Dipolar Aprotic Solvent for Aliphatic Nucleophilic Substitution Reactions

2011 ◽  
Vol 76 (5) ◽  
pp. 1425-1435 ◽  
Author(s):  
Pengju Ji ◽  
John Atherton ◽  
Michael I. Page
Keyword(s):  
Nucleophilic Substitution ◽  
Liquid Ammonia ◽  
Aprotic Solvent ◽  
Substitution Reactions ◽  
Dipolar Aprotic Solvent ◽  
Nucleophilic Substitution Reactions

Enthalpies of transfer of transition states in the Menshutkin reaction from a polar protic to a dipolar aprotic solvent

1971 ◽  
Vol 36 (13) ◽  
pp. 1792-1795 ◽  
Author(s):  
Paul Haberfield ◽  
Abraham Nudelman ◽  
Allen Bloom ◽  
Richard Romm ◽  
Henry Ginsberg
Keyword(s):  
Aprotic Solvent ◽  
Transition States ◽  
Dipolar Aprotic Solvent ◽  
Enthalpies Of Transfer ◽  
Menshutkin Reaction

Réactions dans le sulfolane. VI. Etude de solutions des acides perchlonque, fluorosulfurique, pyrosulfurique et hexachloroantimonique

1970 ◽  
Vol 48 (15) ◽  
pp. 2353-2359 ◽  
Author(s):  
R. L. Benoit ◽  
C. Buisson ◽  
G. Choux
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Aprotic Solvent ◽  
Strong Acid ◽  
Acid Strength ◽  
Protic Solvent ◽  
Dilute Solution ◽  
Conductivity Data ◽  
Dipolar Aprotic Solvent ◽  
Nuclear Magnetic

Nuclear magnetic resonance and certain conductivity data are reported for solutions of perchloric and fluorosulfuric acids in sulfolane. Additional measurements were made on solutions of disulfuric and hexachloroantimony (V) acids. HSbCl6 is a strong acid in this weakly basic dipolar aprotic solvent. HClO4, HSO3F, and H2S2O7 are incompletely dissociated with K = 10−2.7, 10−3.3, and ~ 10−5, respectively. The acid strength in dilute solution in sulfolane follows the order HClO4 > HSO3F > H2S2O7, which differs from that known in H2SO4 which is a strongly associated polar protic solvent.

1,4-Addition polymerization of 1,4-bis(4-benzylpyridinium)butadiyne triflate in a dipolar aprotic solvent

2002 ◽  
Vol 40 (20) ◽  
pp. 3534-3541 ◽  
Author(s):  
Yoichiro Iwase ◽  
Koichi Kondo ◽  
Kenji Kamada ◽  
Koji Ohta
Keyword(s):  
Aprotic Solvent ◽  
Dipolar Aprotic Solvent ◽  
Addition Polymerization
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