| Year |
Citation |
Score |
| 2012 |
Guchhait SK, Chaudhary V, Madaan C. A chemoselective Ugi-type reaction in water using TMSCN as a functional isonitrile equivalent: Generation of heteroaromatic molecular diversity Organic and Biomolecular Chemistry. 10: 9271-9277. PMID 23104509 DOI: 10.1039/C2Ob26733K |
0.708 |
|
| 2012 |
Sarkar A, Raha Roy S, Kumar D, Madaan C, Rudrawar S, Chakraborti AK. Lack of correlation between catalytic efficiency and basicity of amines during the reaction of aryl methyl ketones with DMF-DMA: an unprecedented supramolecular domino catalysis. Organic & Biomolecular Chemistry. 10: 281-6. PMID 22057389 DOI: 10.1039/C1Ob06043K |
0.457 |
|
| 2012 |
Madaan C, Saraf S, Priyadarshani G, Reddy PP, Guchhait SK, Kunwar AC, Sridhar B. One-pot, three-step copper-catalyzed five-/four-component reaction constructs polysubstituted oxa(thia)zolidin-2-imines Synlett. 23: 1955-1959. DOI: 10.1055/S-0032-1316606 |
0.715 |
|
| 2012 |
Madaan C, Saraf S, Priyadarshani G, Reddy PP, Guchhait SK, Kunwar AC, Sridhar B. ChemInform Abstract: One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201247117 |
0.374 |
|
| 2011 |
Baviskar AT, Madaan C, Preet R, Mohapatra P, Jain V, Agarwal A, Guchhait SK, Kundu CN, Banerjee UC, Bharatam PV. N-fused imidazoles as novel anticancer agents that inhibit catalytic activity of topoisomerase IIα and induce apoptosis in G1/S phase. Journal of Medicinal Chemistry. 54: 5013-30. PMID 21644529 DOI: 10.1021/Jm200235U |
0.533 |
|
| 2011 |
Guchhait SK, Madaan C. Groebke-Blackburn-Bienaymé multicomponent reaction in scaffold-modification of adenine, guanine, and cytosine: Synthesis of aminoimidazole-condensed nucleobases Tetrahedron Letters. 52: 56-58. DOI: 10.1016/J.Tetlet.2010.10.143 |
0.674 |
|
| 2010 |
Guchhait SK, Madaan C. Towards molecular diversity: Dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile Organic and Biomolecular Chemistry. 8: 3631-3634. PMID 20574586 DOI: 10.1039/C0Ob00022A |
0.704 |
|
| 2010 |
Guchhait SK, Jadeja K, Madaan C. ChemInform Abstract: A New Process of Multicomponent Povarov Reaction-Aerobic Dehydrogenation: Synthesis of Polysubstituted Quinolines. Cheminform. 41. DOI: 10.1002/CHIN.201010154 |
0.419 |
|
| 2010 |
Guchhait SK, Madaan C, Thakkar BS. ChemInform Abstract: A Highly Flexible and Efficient Ugi-Type Multicomponent Synthesis of Versatile N-Fused Aminoimidazoles. Cheminform. 41. DOI: 10.1002/CHIN.201008127 |
0.398 |
|
| 2009 |
Guchhait SK, Madaan C, Thakkar BS. A highly flexible and efficient ugi-type multicomponent synthesis of versatile n-fused aminoimidazoles Synthesis. 3293-3300. DOI: 10.1055/S-0029-1216916 |
0.709 |
|
| 2009 |
Guchhait SK, Madaan C. An efficient, regioselective, versatile synthesis of N-fused 2- and 3-aminoimidazoles via Ugi-type multicomponent reaction mediated by zirconium(IV) chloride in polyethylene glycol-400 Synlett. 628-632. DOI: 10.1055/S-0028-1087915 |
0.728 |
|
| 2009 |
Guchhait SK, Jadeja K, Madaan C. A new process of multicomponent Povarov reaction-aerobic dehydrogenation: synthesis of polysubstituted quinolines Tetrahedron Letters. 50: 6861-6865. DOI: 10.1016/J.Tetlet.2009.09.125 |
0.682 |
|
| 2009 |
Guchhait SK, Madaan C. ChemInform Abstract: An Efficient, Regioselective, Versatile Synthesis of N-Fused 2- and 3-Aminoimidazoles via Ugi-Type Multicomponent Reaction Mediated by Zirconium(IV) Chloride in Polyethylene Glycol-400. Cheminform. 40. DOI: 10.1002/chin.200928138 |
0.531 |
|
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