60 results on '"Patel, P. K."'
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2. ChemInform Abstract: Studies on 4‐Thiazolidinones. Part 9. Synthesis and Antimicrobial Activity of 2‐(2′‐Aryl‐4‐thiazolidinon‐3′‐yl)‐4‐(2′′‐methyl‐4′′‐ hydroxy‐5′′‐isopropylphenyl)thiazoles.
3. ChemInform Abstract: Studies on Diphenyl Sulfones. Preparation and Antimicrobial Activity of p,p′‐Bis(2‐aryl‐1,3,4‐oxadiazol‐5‐yl)diphenyl Sulfones and p,p′‐Bis( 3‐chloro‐4‐aryl‐2‐azetidinon‐1‐ylaminocarbonyl)diphenyl Sulfones.
4. ChemInform Abstract: Cu(II) Catalyzed Imine C—H Functionalization Leading to Synthesis of 2,5‐Substituted 1,3,4‐Oxadiazoles.
5. ChemInform Abstract: The Oxidative Cleavage of an anti-Hugerschoff Product: A Mild Environmentally Benign One-Pot Synthesis of Ureas from Isothiocyanates.
6. ChemInform Abstract: Synthesis and Antimicrobial Activity of Some 7‐Aryl‐5,6‐dihydro‐14‐aza[1]benzopyrano[3,4‐b]phenanthren‐8H‐ones.
7. ChemInform Abstract: Tandem Regioselective Synthesis of Tetrazoles and Related Heterocycles Using Iodine.
8. ChemInform Abstract: Bromineless Bromine as an Efficient Desulfurizing Agent for the Preparation of Cyanamides and 2‐Aminothiazoles from Dithiocarbamate Salts.
9. ChemInform Abstract: Sonochemistry: The Effect of Sonic Waves on Chemical Systems
10. ChemInform Abstract: Bernthsen Synthesis, Antimicrobial Activities and Cytotoxicity of Acridine Derivatives.
11. ChemInform Abstract: Synthesis and Antimicrobial Activity of 2-(3′-Chloro-4′-aryl-2′- azetidinon-1′-yl)-4-(2′′-methyl-4′′-hydroxy-5′′-iso propylphenyl) thiazoles.
12. ChemInform Abstract: Efficient Preparation of Isothiocyanates from Dithiocarbamates Using Bromineless Brominating Reagent.
13. ChemInform Abstract: Synthesis and Antimicrobial Screening of Some 3‐[4‐(3‐Aryl‐1‐phenyl‐1H‐pyrazol‐4‐yl)‐6‐aryl‐pyridin‐2‐yl] (III) and 4‐Methyl‐3‐phenyl‐6‐ [4‐(3‐aryl‐1‐phenyl‐1H‐pyrazol‐4‐yl)‐6‐aryl‐pyridin‐2yl] Coumarins (V).
14. ChemInform Abstract: The Thiocarbonyl “S” Is Softer than Thiolate “S”: A Catalyst‐Free One‐Pot Synthesis of Isothiocyanates in Water.
15. ChemInform Abstract: Hypervalent Iodine(III)‐Mediated Oxidation of Aldoximes to N‐Acetoxy or N‐Hydroxy Amides.
16. ChemInform Abstract: A Greener Synthetic Protocol for the Preparation of Carbodiimide.
17. ChemInform Abstract: A One‐Pot Preparation of Cyanamide from Dithiocarbamate Using Molecular Iodine.
18. ChemInform Abstract: Copper(I)‐Catalyzed Cascade Synthesis of 2‐Substituted 1,3‐Benzothiazoles: Direct Access to Benzothiazolones.
19. ChemInform Abstract: Intra‐ and Intermolecular C—S Bond Formation Using a Single Catalytic System: First Direct Access to Arylthiobenzothiazoles.
20. ChemInform Abstract: Acyl‐Isothiocyanates as Efficient Thiocyanate Transfer Reagents.
21. ChemInform Abstract: An Efficient Synthesis of Cyanamide from Amine Promoted by a Hypervalent Iodine(III) Reagent.
22. ChemInform Abstract: Molecular Iodine Mediated Preparation of Isothiocyanates from Dithiocarbamic Acid Salts.
23. ChemInform Abstract: Copper(I)‐Catalyzed Synthesis of Substituted 2‐Mercapto Benzimidazoles.
24. ChemInform Abstract: Desulfurization Mediated by Hypervalent Iodine(III): A Novel Strategy for the Construction of Heterocycles.
25. ChemInform Abstract: It Is “2‐Imino‐4‐thiazolidinones” and Not Thiohydantoins as the Reaction Product of 1,3‐Disubstituted Thioureas and Chloroacetylchloride.
26. ChemInform Abstract: Syntheses and Regiochemistry of Enol Addition to 9‐Phenyl‐9H‐xanthen‐9‐ol.
27. ChemInform Abstract: A Convenient One‐Pot Synthesis of Thiazol‐2‐imines: Application in the Construction of Pifithrin Analogues.
28. ChemInform Abstract: Hypervalent Iodine(III)‐Mediated Regioselective N‐Acylation of 1,3‐Disubstituted Thioureas.
29. ChemInform Abstract: A New Facile Synthetic Method for the Construction of 1,3‐Oxathiolan‐2‐ylidenes.
30. 3‐Aryl‐1‐benzoylthioureas with α‐Bromoketones in Water Form 2‐N‐Benzoyl‐3‐arylthiazol‐2(3H)‐imines, Not 3‐Aryl‐1‐benzoylimidazoline‐2‐thiones.
31. Aqueous‐Mediated N‐Alkylation of Amines.
32. A One‐Pot Synthesis of 1,4‐Dithiins and 1,4‐Benzodithiins from Ketones Using the Recyclable Reagent 1,1′‐(Ethane‐1,2‐diyl)dipyridinium Bistribromide (EDPBT).
33. Stereospecific Cross‐Coupling of α‐(Thiocarbamoyl)organostannanes with Alkenyl, Aryl, and Heteroaryl Iodides.
34. A New Recyclable Ditribromide Reagent for Efficient Bromination under Solvent Free Condition.
35. Design, Synthesis and Pharmacological Evaluation of Some Novel 2‐(4‐Nitrophenyl)‐3‐methylthio‐3‐(substituted)arylamino Acrylamides as Potential Antiinflammatory Agents.
36. Synthesis of Novel 6‐Substituted‐aminopyridine‐2(H)‐ones.
37. Chemoselective Thioacetalization and Transthioacetalization of Carbonyl Compounds Catalyzed by Tetrabutylammonium Tribromide (TBATB).
38. Chemoselective Acylation of Amines in Aqueous Media.
39. Inhibition of Estrone Sulfatase (ES) by Alkyl and Cycloalkyl Ester Derivatives of 4‐[(Aminosulfonyl)oxy] Benzoic Acid.
40. Asymmetric Total Synthesis and Stereochemical Elucidation of the Antitumor Agent PM‐94128.
41. Peroxovanadium‐Catalyzed Oxidative Esterification of Aldehydes.
42. Diastereoselective Addition of Terminal Alkynes to Chiral Nitrones: Asymmetric Synthesis of Propargylic N‐Hydroxylamines.
43. V2O5—H2O2: A Convenient Reagent for the Direct Oxidation of Acetals to Esters.
44. Design, Synthesis and Biochemical Evaluation of AC Ring Mimics as Novel Inhibitors of the Enzyme Estrone Sulfatase (ES).
45. ChemInform Abstract: Compatibility of the Thioamide Functional Group with β‐Sheet Secondary Structure: Incorporation of a Thioamide Linkage into a β‐Hairpin Peptide.
46. ChemInform Abstract: Hydrophobicity, a Physicochemical Factor in the Inhibition of the Enzyme Estrone Sulfatase (ES).
47. ChemInform Abstract: Tetrabutylammonium Tribromide (TBATB)‐Promoted Tetrahydropyranylation/Depyranylation of Alcohols.
48. ChemInform Abstract: Novel Inhibitors of the Enzyme Estrone Sulfatase (ES).
49. ChemInform Abstract: Tetrabutylammonium Tribromide (TBATB)—MeOH: An Efficient Chemoselective Reagent for the Cleavage of tert‐Butyldimethylsilyl (TBDMS) Ethers.
50. ChemInform Abstract: A Catalytic Oxidative Esterification of Aldehydes Using V2O5—H2O2.
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