| Year |
Citation |
Score |
| 2016 |
Bera S, Chatterjee B, Mondal D. Construction of quaternary stereocentres on carbohydrate scaffolds Rsc Advances. 6: 77212-77242. DOI: 10.1039/C6Ra13898E |
0.332 |
|
| 2016 |
Bera S, Mondal D, Palit S, Schweizer F. Structural modifications of the neomycin class of aminoglycosides Medchemcomm. 7: 1499-1534. DOI: 10.1039/C6Md00079G |
0.46 |
|
| 2015 |
Bera S, Mondal D, Martin JT, Singh M. Potential effect of ultrasound on carbohydrates. Carbohydrate Research. 410: 15-35. PMID 25954862 DOI: 10.1016/J.Carres.2015.02.008 |
0.362 |
|
| 2015 |
Bera S, Mondal D, Chatterjee B. An expedient strategy towards an advanced pyrrolidine intermediate for the synthesis of pyrrolizidine alkaloids Chemistry Letters. 44: 1260-1262. DOI: 10.1246/Cl.150188 |
0.425 |
|
| 2014 |
Chatterjee B, Bera S, Mondal D. Julia-Kocienski olefination: A key reaction for the synthesis of macrolides Tetrahedron Asymmetry. 25: 1-55. DOI: 10.1016/J.Tetasy.2013.09.027 |
0.39 |
|
| 2013 |
Bera S, Mondal D, Singh M, Kale RK. Advances in serinals for asymmetric synthesis Tetrahedron. 69: 969-1011. DOI: 10.1016/J.Tet.2012.11.054 |
0.379 |
|
| 2012 |
Banerjee I, Douaisi MP, Mondal D, Kane RS. Light-activated nanotubeporphyrin conjugates as effective antiviral agents Nanotechnology. 23. PMID 22361811 DOI: 10.1088/0957-4484/23/10/105101 |
0.469 |
|
| 2011 |
Mondal D, Zhanel GG, Schweizer F. Synthesis and antibacterial properties of carbohydrate-templated lysine surfactants. Carbohydrate Research. 346: 588-94. PMID 21316648 DOI: 10.1016/J.Carres.2011.01.025 |
0.538 |
|
| 2011 |
Joshi A, Kate S, Poon V, Mondal D, Boggara MB, Saraph A, Martin JT, McAlpine R, Day R, Garcia AE, Mogridge J, Kane RS. Structure-based design of a heptavalent anthrax toxin inhibitor. Biomacromolecules. 12: 791-6. PMID 21302959 DOI: 10.1021/Bm101396U |
0.494 |
|
| 2010 |
Banerjee I, Mondal D, Martin J, Kane RS. Photoactivated antimicrobial activity of carbon nanotube - Porphyrin conjugates Langmuir. 26: 17369-17374. PMID 20931992 DOI: 10.1021/La103298E |
0.476 |
|
| 2010 |
Mondal D, Schweizer F. Synthesis of allose-templated hydroxyornithine and hydroxyarginine analogs. Carbohydrate Research. 345: 1533-40. PMID 20478556 DOI: 10.1016/J.Carres.2010.04.017 |
0.572 |
|
| 2010 |
Mondal D, Bera S. A Synthetic View of an Analogue of the Spiro-β-lactone-γ-lactam Ring in Oxazolomycins and Lajollamycin Synthesis. 2010: 3301-3308. DOI: 10.1055/S-0030-1257872 |
0.374 |
|
| 2008 |
Zhang K, Mondal D, Zhanel GG, Schweizer F. Synthesis of glucose-templated lysine analogs and incorporation into the antimicrobial dipeptide sequence kW-OBn. Carbohydrate Research. 343: 1644-52. PMID 18452902 DOI: 10.1016/J.Carres.2008.04.018 |
0.576 |
|
| 2008 |
Mondal D, Schweizer F. Alkylation reactions using a galactose-based β-keto ester enolate and conversion into β-C-galactosides Synlett. 2475-2478. DOI: 10.1055/S-2008-1078176 |
0.528 |
|
| 2007 |
Mohapatra DK, Mondal D, Gurjar MK. Towards the Enantioselective Synthesis of anti-HIV Agents Litseaverticillols C and K from D-Glucose. Cheminform. 38. DOI: 10.1016/J.Tet.2007.01.037 |
0.557 |
|
| 2007 |
Mohapatra DK, Mondal D, Gurjar MK. Towards the enantioselective synthesis of anti-HIV agents litseaverticillols C and K from d-glucose Tetrahedron. 63: 2613-2621. DOI: 10.1016/J.TET.2007.01.037 |
0.485 |
|
| 2007 |
Gurjar MK, Mondal D, Ravindranadh SV, Chorghade MS. Clay-Mediated Selective Hydrolysis of 5′-O-Acetyl-2′,3′-isopropylidene/Cyclohexylidene Nucleosides. Cheminform. 38. DOI: 10.1002/CHIN.200707184 |
0.421 |
|
| 2006 |
Gurjar MK, Mondal D, Ravindranadh SV, Chorghade MS. Clay‐Mediated Selective Hydrolysis of 5′‐O‐Acetyl‐2′,3′‐isopropylidene/Cyclohexylidene Nucleosides Synthetic Communications. 36: 2321-2327. DOI: 10.1080/00397910600639968 |
0.478 |
|
| 2006 |
Mohapatra DK, Mondal D, Chorghade MS, Gurjar MK. General strategy for a short and efficient synthesis of 3-hydroxy-4-methylprolines (HMP) Tetrahedron Letters. 47: 9215-9219. DOI: 10.1016/J.Tetlet.2006.10.137 |
0.568 |
|
| 2006 |
Mohapatra DK, Mondal D, Gonnade RG, Chorghade MS, Gurjar MK. Synthesis of the spiro fused β-lactone-γ-lactam segment of oxazolomycin Tetrahedron Letters. 47: 6031-6035. DOI: 10.1016/J.Tetlet.2006.06.117 |
0.532 |
|
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