Umpolung reactions in an ionic liquid catalyzed by electrogenerated N-heterocyclic carbenes. Synthesis of saturated esters from activated α,β-unsaturated aldehydes

2012 ◽  
Vol 48 (43) ◽  
pp. 5361 ◽  
Author(s):  
Marta Feroci ◽  
Isabella Chiarotto ◽  
Monica Orsini ◽  
Romina Pelagalli ◽  
Achille Inesi
2012 ◽  
Vol 14 (10) ◽  
pp. 2738 ◽  
Author(s):  
Dajiang (D. J.) Liu ◽  
Yuetao Zhang ◽  
Eugene Y.-X. Chen

2018 ◽  
Vol 107 ◽  
pp. 82-88 ◽  
Author(s):  
Sofiem Garmendia ◽  
Romain Lambert ◽  
Anne-Laure Wirotius ◽  
Joan Vignolle ◽  
Andrew P. Dove ◽  
...  

2007 ◽  
Vol 62 (14) ◽  
pp. 3660-3671 ◽  
Author(s):  
Pasi Virtanen ◽  
Hannu Karhu ◽  
Krisztian Kordas ◽  
Jyri-Pekka Mikkola

2010 ◽  
Vol 8 (5) ◽  
pp. 992-998 ◽  
Author(s):  
Saravanakumar Shanmuganathan ◽  
Olaf Kühl ◽  
Peter Jones ◽  
Joachim Heinicke

AbstractThe reaction of chloroethyltrimethylsilylether with 1-methylimidazole furnishes an ionic liquid that undergoes methanolysis to crystalline 2-hydroxyethylimidazolium chloride (crystal structure presented). Conversion to defined hydroxyethylimidazol-2-ylidene nickel complexes failed, but was accomplished with 1-methyl-3-acetophenyl-imidazolium bromide. The bis(NHC⋂O−) nickel(II) chelate is formed, rather than a methallylnickel monochelate, but with nickelocene a monochelate NiCp complex was detected. The bulky 1-(2,6-diisopropylphenyl)-3-(2’-phenyl-enolato)-imidazol-2-ylidene allylpalladium chloride was obtained in pure form. Attempts to generate catalysts for ethylene oligomerization by in situ techniques have failed so far whereas P⋂O− ligands, comparable by the P-C diagonal relationship, provide active catalysts.


2017 ◽  
Vol 28 (6) ◽  
pp. 1021-1029 ◽  
Author(s):  
Thyago S. Rodrigues ◽  
Denis Lesage ◽  
Wender A. da Silva ◽  
Richard B. Cole ◽  
Günter Ebeling ◽  
...  

2011 ◽  
Vol 64 (8) ◽  
pp. 1158 ◽  
Author(s):  
Roxanne L. Atienza ◽  
Karl A. Scheidt

N-heterocyclic carbenes (NHCs) promote the addition of 1,1-bis(phenylsulfonyl)ethylene to the α-position of α,β-unsaturated aldehydes. The proposed reaction pathway for this Rauhut–Currier-type reaction includes an unusual conjugate addition of an NHC to a bis-vinyl sulfone.


RSC Advances ◽  
2012 ◽  
Vol 2 (8) ◽  
pp. 3201 ◽  
Author(s):  
Priscila M. Lalli ◽  
Thyago S. Rodrigues ◽  
Aline M. Arouca ◽  
Marcos N. Eberlin ◽  
Brenno A. D. Neto

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