2009
DOI: 10.1039/b911388f
|View full text |Cite
|
Sign up to set email alerts
|

Solvent-free three component Strecker reaction of ketones using highly recyclable and hydrophobic sulfonic acid based nanoreactors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
54
0

Year Published

2011
2011
2020
2020

Publication Types

Select...
9

Relationship

4
5

Authors

Journals

citations
Cited by 70 publications
(54 citation statements)
references
References 53 publications
0
54
0
Order By: Relevance
“…Accordingly, the total weight loss reaches 22.4%. Due to the attributes described above for the use of sulfonated ordered nanoporous carbon in catalysis and our current interest in developing environmentally benign synthetic protocols for different organic transformations [41,[54][55][56], we reveal herein for the first time, highly reusable CMK-5-SO 3 H catalyzed trimethylsilylation of a wide variety of alcohols and phenols at ambient temperature (Scheme 1).…”
Section: Resultsmentioning
confidence: 97%
“…Accordingly, the total weight loss reaches 22.4%. Due to the attributes described above for the use of sulfonated ordered nanoporous carbon in catalysis and our current interest in developing environmentally benign synthetic protocols for different organic transformations [41,[54][55][56], we reveal herein for the first time, highly reusable CMK-5-SO 3 H catalyzed trimethylsilylation of a wide variety of alcohols and phenols at ambient temperature (Scheme 1).…”
Section: Resultsmentioning
confidence: 97%
“…18 Protocols based on TMSCN often require variety of Lewis or Bronsted acid catalyst such as Pr(OTf) 3 , 19 Yb(OTf), 20 Cu(OTf) 2 32 Montmorillonite KSF, 33 polymer-supported Sc(OTf) 3,34 silica-supported heteropoly acids, 35 cellulose sulfuric acid, 36 alumina supported tungstosilicic acid, 37 SBA-15 supported sulfonic acid, 38 sulfamic acid functionalized magnetic Fe 3 O 4 nanoparticles, 39 H 2 SO 4/ Silica gel, 40 silica-bonded S-sulfonic acid, 41 sulphated tungstate, 42 MCM-41 anchored sulfonic acid, 43 nano magnetic sulfated zirconia, 44 sulfamic acid, 45 and xanthan sulfuric acid. 46 However, many of these methods suffer from several shortcomings such as low reactivity, unsatisfactory yields, moisture sensitive nature, longer reaction time, harsh reaction conditions, tedious workup, generation of toxic byproducts, use of expensive, metal-based, corrosive/toxic catalysts or reagent.…”
Section: Scheme 1 Schematic Representation Of Sulfated Polyborate Camentioning
confidence: 99%
“…Therefore, in connection with our research programs aimed at the utility of this nanostructured solid acids for different organic transformations, [48][49][50][51][52] herein, we investigated the application of SBA-15-Ph-Pr-SO 3 H as a highly effective and reusable catalyst in tetrahydropyranylation of alcohols and phenols in solvent-free conditions at ambient temperatures (Figures 1 and 2). …”
Section: Introductionmentioning
confidence: 99%
“…Recently, we demonstrated the application of a heterogeneous and hydrophobic sulfonic acid nanoreactor with both acidic sites and phenyl groups inside the mesochannel of SBA-15 as an efficient, environmentally benign, and highly recoverable catalyst for both Pechmann [48] and Strecker [49] reactions. Therefore, in connection with our research programs aimed at the utility of this nanostructured solid acids for different organic transformations, [48][49][50][51][52] herein, we investigated the application of SBA-15-Ph-Pr-SO 3 H as a highly effective and reusable catalyst in tetrahydropyranylation of alcohols and phenols in solvent-free conditions at ambient temperatures (Figures 1 and 2).…”
Section: Introductionmentioning
confidence: 99%