Our system is currently under heavy load due to increased usage. We're actively working on upgrades to improve performance. Thank you for your patience.
1997
DOI: 10.1016/s0040-4039(97)00554-6
|View full text |Cite
|
Sign up to set email alerts
|

Moisture Stable Dialkylimidazolium Salts as Heterogeneous and Homogeneous Lewis Acids in the Diels-Alder Reaction

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
131
0
4

Year Published

2000
2000
2011
2011

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 241 publications
(136 citation statements)
references
References 6 publications
1
131
0
4
Order By: Relevance
“…The crude residue was purified via flash chromatography (100% ethyl acetate) to provide the desired compound. 1 Synthesis and Decoloration of Nonracemic Low-Melting Organic Salts. Room-temperature nonracemic ILs (a) and (b) ( Figure 2) were prepared according to a previously published procedure.…”
Section: Methodsmentioning
confidence: 99%
“…The crude residue was purified via flash chromatography (100% ethyl acetate) to provide the desired compound. 1 Synthesis and Decoloration of Nonracemic Low-Melting Organic Salts. Room-temperature nonracemic ILs (a) and (b) ( Figure 2) were prepared according to a previously published procedure.…”
Section: Methodsmentioning
confidence: 99%
“…Estes compostos despertaram grande interesse em domínios como a eletroquímica 9 , baterias, solventes para análise espectroscópica de compostos metálicos 10 e como solventes e catalisadores ácidos para reações orgânicas 4,[11][12][13] . No início da década de noventa, misturas ternárias contendo cloreto de 1-n-butil-3-metilimidazólio (BMI.Cl) 14 , tricloreto de alumínio e um halogeneto de alquilalumínio (AlR x Cl 3-x ) foram introduzidas como solventes para a dimerização catalítica de olefinas em meio bifásico, utilizando catalisadores de ní-quel.…”
Section: Esquemaunclassified
“…Ionic liquids offer interesting and useful features that are advantageous to organic reactions such as negligible vapor pressure, nonflammability, high thermal stability, and easy reusability. In this regard, ionic liquids have been successfully used in the Friedel-Crafts reaction [31][32][33], hydrogenation [34][35][36], Diels-Alder reactions [37][38][39], Mizoroki-Heck, Suzuki-Miyaura, Sonogashira, and olefin metathesis reactions [40][41][42][43][44], Michael additions [45], oxidation [46][47][48][49][50][51][52][53][54], condensation reaction [55][56][57][58][59], formation of imines [60], 1,2-rearrangement [61], esterification of carboxylic acids and carboxylates [62][63][64][65], Williamson ether synthesis [66][67][68][69][70][71][72], and the Grignard reaction [73,74]. We have reported efficient methods for the esterification of carboxylic acids and phosphonic acids with trialkyl orthoacetate in ionic liquid <...>…”
Section: Introductionmentioning
confidence: 99%