Chemoselective N-nitrosation of secondary amines under heterogeneous and mild conditions via in situ generation of HNO2

2009 ◽  
Vol 20 (4) ◽  
pp. 415-419 ◽  
Author(s):  
Arash Ghorbani-Choghamarani ◽  
Hamid Goudarziafshar ◽  
Somaieh Rezaee ◽  
Saiedeh Shima Mortazavi
Keyword(s):  
Secondary Amines ◽  
Mild Conditions ◽  
In Situ Generation

ChemInform Abstract: Chemoselective N-Nitrosation of Secondary Amines under Heterogeneous and Mild Conditions via in situ Generation of HNO2.

ChemInform ◽  
2009 ◽  
Vol 40 (35) ◽  
Author(s):  
Arash Ghorbani-Choghamarani ◽  
Hamid Goudarziafshar ◽  
Somaieh Rezaee ◽  
Saiedeh Shima Mortazavi
Keyword(s):  
Secondary Amines ◽  
Mild Conditions ◽  
In Situ Generation

In Situ Generation of Brønsted Acidity in the Pd-I Bifunctional Catalysts for Selective Reductive Etherification of Carbonyl Compounds under Mild Conditions

ACS Catalysis ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 2940-2948 ◽  
Author(s):  
Dan Wu ◽  
Willinton Y. Hernández ◽  
Songwei Zhang ◽  
Evgeny I. Vovk ◽  
Xiaohong Zhou ◽  
...  
Keyword(s):  
Carbonyl Compounds ◽  
Bifunctional Catalysts ◽  
Brønsted Acidity ◽  
Mild Conditions ◽  
Brönsted Acidity ◽  
In Situ Generation

Silica Chloride/NaNO 2 as a Novel Heterogeneous System for the Oxidation of 1,4-Dihydropyridines Under Mild Conditions via In Situ Generation of NOCl

2003 ◽  
Vol 178 (8) ◽  
pp. 1709-1715 ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Farhad Shirini ◽  
Arash Ghorbani Choghamarani ◽  
Iraj Mohammadpoor-Baltork
Keyword(s):  
Heterogeneous System ◽  
Mild Conditions ◽  
In Situ Generation

scholarly journals REGIOSELECTIVE AND FACILE OXIDATIVE THIOCYANATION OF ANILINES AND INDOLES WITH TRANS-3,5‐DIHYDROPEROXY‐3,5‐DIMETHYL‐1,2‐DIOXOLANE

2014 ◽  
Vol 10 (8) ◽  
pp. 3088-3096 ◽  
Author(s):  
Davood Azarifar ◽  
Maryam Golbaghi ◽  
Mahtab Pirveisian ◽  
Zohreh Najminejad
Keyword(s):  
Room Temperature ◽  
Reaction Times ◽  
Sodium Thiocyanate ◽  
Oxidative Potential ◽  
Mild Conditions ◽  
In Situ Generation

Oxidative potential of trans‐3,5‐dihydroperoxy‐3,5‐dimethyl‐1,2‐dioxolane (DHPODMDO) has been explored in the facile thiocyanation of anilines and indoles through the efficient and in situ generation of SCN+ ion from sodium thiocyanate. The reactions proceed with regioselectivity under mild conditions at room temperature to afford the respective thiocyanate derivatives in excellent yields and low reaction times.

ChemInform Abstract: Chemoselective N-Nitrosation of Secondary Amines under Mild and Heterogeneous Conditions via in situ Generation of NOCl.

ChemInform ◽  
2001 ◽  
Vol 32 (8) ◽  
pp. no-no
Author(s):  
Mohammad Ali Zolfigol ◽  
Farhad Shirini ◽  
Arash Ghorbani Choghamarani ◽  
Abolfazl Taqian-Nasab ◽  
Hassan Keypour ◽  
...  
Keyword(s):  
Secondary Amines ◽  
In Situ Generation

scholarly journals MOF-Mediated Synthesis of Supported Fe-doped Pd Nanoparticles under Mild Conditions for Magnetically Recoverable Catalysis

2020 ◽  
Author(s):  
Guillermo Minguez Espallargas ◽  
Mohanad D. Darawsheh ◽  
Dr. Mónica Giménez Marqués ◽  
Marcelo E. Domine ◽  
Pascual Oña-Burgos ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Active Sites ◽  
Pd Nanoparticles ◽  
Reusable Catalyst ◽  
Synthetic Approach ◽  
Promising Alternative ◽  
Mild Conditions ◽  
Catalytic Materials ◽  
In Situ Generation

MOF-driven synthesis is considered as a promising alternative for the development of new catalytic materials with well-designed active sites. This synthetic approach is used here to gradually transform a new bimetallic MOF, composed of Pd and Fe as metal components, via the in situ generation of aniline under mild conditions. This methodology results in a compositionally homogeneous nanocomposite formed by Fedoped Pd nanoparticles and these, in turn, supported on an iron oxide-doped carbon. The nanocomposite has been fully characterized by several techniques such as IR, Raman, TEM, XPS, XAS, among others. The performance of this nanocomposite as an heterogeneous catalyst for hydrogenation of nitroarenes and nitrobenzene coupling with benzaldehyde has been evaluated, proving it to be an efficient and reusable catalyst.

ChemInform Abstract: Oxidation of Urazoles via in situ Generation of Cl+ by Using N,N,2,3,4,5,6-Heptachloroaniline or a UHP/MCln System under Mild Conditions.

ChemInform ◽  
2010 ◽  
Vol 33 (6) ◽  
pp. no-no
Author(s):  
Mohammad Ali Zolfigol ◽  
Mojtaba Bagherzadeh ◽  
Gholamabbass Chehardoli ◽  
Shadpour E. Mallakpour ◽  
Manochehr Mamaghani
Keyword(s):  
Mild Conditions ◽  
In Situ Generation

Cyanide-Mediated Synthesis of Sulfones and Sulfonamides from Vinyl Sulfones

Synlett ◽  
2019 ◽  
Vol 31 (05) ◽  
pp. 455-458
Author(s):  
Tamal Roy ◽  
Ji-Woong Lee
Keyword(s):  
High Selectivity ◽  
Reaction Pathway ◽  
Secondary Amines ◽  
Mechanistic Study ◽  
Facile Synthesis ◽  
Primary And Secondary Amines ◽  
In Situ Generation ◽  
High Yields

We report a facile synthesis of sulfones, β-keto sulfones, and sulfonamides from vinyl sulfones via an addition–elimination sequence where in situ generation of nucleophilic sulfinate ion is mediated by cyanide. The use vinyl sulfones renders high selectivity for S-alkylation to produce sulfones in high yields. In the presence of N-bromosuccinimide, primary and secondary amines underwent sulfonamide formation. A preliminary mechanistic study showed the formation of acrylonitrile as an innocent byproduct, without interfering with the desired reaction pathway while generating a sulfinate nucleophile.

ChemInform Abstract: H5IO6/KI: A New Combination Reagent for Iodination of Aromatic Amines, and Trimethylsilylation of Alcohols and Phenols Through in situ Generation of Iodine under Mild Conditions.

ChemInform ◽  
2010 ◽  
Vol 41 (31) ◽  
pp. no-no
Author(s):  
Mohammad Ali Zolfigol ◽  
Ardeshir Khazaei ◽  
Eskandar Kolvari ◽  
Nadiya Koukabi ◽  
Hamid Soltani ◽  
...  
Keyword(s):  
Aromatic Amines ◽  
New Combination ◽  
Mild Conditions ◽  
In Situ Generation
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