2011
DOI: 10.1002/chin.201132039
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Sulfated Tungstate: An Efficient Catalyst for the Ritter Reaction.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2015
2015
2015
2015

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…This reaction consists on the addition of nitriles to a wide variety of compounds capable of forming carbenium ions, such as alkenes, alcohols, carboxylic acids and esters, in the presence of concentrated sulphuric acid [2,3,4,5]. Over the years, improved processes have been reported for the synthesis of N-alkyl amides, via acid catalyzed Ritter reaction under homogeneous [6,7] and heterogeneous conditions [8,9]. Brønsted acid ionic liquids [10] and organic acids, such as 2,4-dinitrobenzenesulfonic acid (DNBSA) [11], obenzenedisulfonimide [12] and pentafluorophenyl ammonium triflate (PFPAT) [13] have also been recently applied as metal-free catalysts in the Ritter reaction.…”
Section: Introductionmentioning
confidence: 99%
“…This reaction consists on the addition of nitriles to a wide variety of compounds capable of forming carbenium ions, such as alkenes, alcohols, carboxylic acids and esters, in the presence of concentrated sulphuric acid [2,3,4,5]. Over the years, improved processes have been reported for the synthesis of N-alkyl amides, via acid catalyzed Ritter reaction under homogeneous [6,7] and heterogeneous conditions [8,9]. Brønsted acid ionic liquids [10] and organic acids, such as 2,4-dinitrobenzenesulfonic acid (DNBSA) [11], obenzenedisulfonimide [12] and pentafluorophenyl ammonium triflate (PFPAT) [13] have also been recently applied as metal-free catalysts in the Ritter reaction.…”
Section: Introductionmentioning
confidence: 99%