Indrajit Das - Publications

2009- CSIR-IICB 
Synthetic Organic Chemistry, Medicinal Chemistry

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Naskar S, Mal K, Maity R, Das I. Recent Advances in the Synthesis and Applications of α‐Ketothioesters Advanced Synthesis & Catalysis. 363: 1160-1184. DOI: 10.1002/adsc.202001191  0.66
2019 Maity R, Das B, Das I. Transition‐Metal‐Free Reduction of α ‐Keto Thioesters with Hydrosilanes at Room Temperature: Divergent Synthesis through Reagent‐Controlled Chemoselectivities Advanced Synthesis & Catalysis. 361: 2347-2353. DOI: 10.1002/ADSC.201900222  0.326
2018 Maity R, Naskar S, Das I. Copper(II)-Catalyzed Reactions of α-Keto Thioesters with Azides via C-C and C-S Bond Cleavages: Synthesis of N-Acylureas and Amides. The Journal of Organic Chemistry. PMID 29393648 DOI: 10.1021/acs.joc.7b03054  0.4
2017 Maity R, Naskar S, Mal K, Biswas S, Das I. Direct Access to 2-Thioxooxazolidin-4-ones and Oxazolidine-2,4-diones from α-Keto Thioesters through Thiolate Transfer Advanced Synthesis & Catalysis. 359: 4405-4410. DOI: 10.1002/ADSC.201701020  0.69
2017 Mal K, Das I. α-Keto Thioesters as Building Blocks for Accessing γ-Hydroxybutenolides and Oxazoles Advanced Synthesis & Catalysis. 359: 2692-2698. DOI: 10.1002/ADSC.201700329  0.697
2016 Zimmermann L, Das I, Désiré J, Sautrey G, Barros R S V, El Khoury M, Mingeot-Leclercq MP, Decout JL. New Broad-spectrum Antibacterial Amphiphilic Aminoglycosides Active Against Resistant Bacteria: From Neamine Derivatives to Smaller Neosamine Analogues. Journal of Medicinal Chemistry. PMID 27690420 DOI: 10.1021/acs.jmedchem.6b00818  0.614
2016 Mal K, Das I. Base Induced Chiral Substituted Furans and Imidazoles from Carbohydrate-Derived 2-Haloenones. The Journal of Organic Chemistry. 81: 932-45. PMID 26745207 DOI: 10.1021/acs.joc.5b02500  0.736
2016 Mal K, Kaur A, Das I. ChemInform Abstract: Chiral Substituted 3-Formylfurans from Carbohydrates: An Expedient Route via N-Bromosuccinimide (NBS)-Mediated Electrophilic Cyclization. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201607127  0.705
2016 Mal K, Naskar S, Sen SK, Natarajan R, Das I. Tandem Chemoselective 1,2-/1,4-Migration of the Thio Group in Keto Thioesters: An Efficient Approach to Substituted Butenolides Advanced Synthesis and Catalysis. DOI: 10.1002/adsc.201600640  0.721
2015 Mal K, Kaur A, Haque F, Das I. PPh3·HBr-DMSO: A Reagent System for Diverse Chemoselective Transformations. The Journal of Organic Chemistry. 80: 6400-10. PMID 25988985 DOI: 10.1021/acs.joc.5b00846  0.756
2015 Mal K, Das S, Maiti NC, Natarajan R, Das I. ZnI2-Catalyzed Diastereoselective [4 + 2] Cycloadditions of β,γ-Unsaturated α-Ketothioesters with Olefins. The Journal of Organic Chemistry. 80: 2972-88. PMID 25730097 DOI: 10.1021/jo5024766  0.772
2015 Mal K, Kaur A, Das I. Chiral Substituted 3-Formylfurans from Carbohydrates: An Expedient Route via N-Bromosuccinimide (NBS)-Mediated Electrophilic Cyclization Asian Journal of Organic Chemistry. DOI: 10.1002/ajoc.201500272  0.703
2014 Mal K, Sharma A, Das I. Gold(III) chloride catalyzed synthesis of chiral substituted 3-formyl furans from carbohydrates: application in the synthesis of 1,5-dicarbonyl derivatives and furo[3,2-c]pyridine. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11932-45. PMID 25077819 DOI: 10.1002/chem.201402286  0.769
2014 Mal K, Sharma A, Maulik PR, Das I. PPh(3)·HBr-DMSO mediated expedient synthesis of γ-substituted β,γ-unsaturated α-ketomethylthioesters and α-bromo enals: application to the synthesis of 2-methylsulfanyl-3(2H)-furanones. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 662-7. PMID 24339245 DOI: 10.1002/chem.201303755  0.765
2012 Das I, Désiré J, Manvar D, Baussanne I, Pandey VN, Décout JL. A peptide nucleic acid-aminosugar conjugate targeting transactivation response element of HIV-1 RNA genome shows a high bioavailability in human cells and strongly inhibits tat-mediated transactivation of HIV-1 transcription. Journal of Medicinal Chemistry. 55: 6021-32. PMID 22698070 DOI: 10.1021/jm300253q  0.599
2008 Das I, Suresh CG, Décout JL, Pathak T. Unusual addition of amines to C-2 of vinyl sulfone-modified-beta-D-pent-2-enofuranosyl carbohydrates: synthesis of a new class of beta-anomeric 2-amino-2,3-dideoxy-D-threo-pentofuranosides. Carbohydrate Research. 343: 1287-96. PMID 18405888 DOI: 10.1016/J.Carres.2008.03.022  0.701
2007 Das I, Pal TK, Pathak T. Diastereoselective michael initiated ring closure on vinyl sulfone-modified carbohydrates: a stereospecific and general route to alpha-substituted cyclopropanes. The Journal of Organic Chemistry. 72: 9181-9. PMID 17956119 DOI: 10.1021/Jo701378D  0.608
2007 Das I, Pal TK, Suresh CG, Pathak T. Diastereoselective C-C bond formation at C-5 of vinyl sulfone-modified hex-5-enofuranosyl carbohydrates: diversity-oriented synthesis of branched-chain sugars and beyond. The Journal of Organic Chemistry. 72: 5523-33. PMID 17580895 DOI: 10.1021/Jo062373+  0.58
2006 Das I, Pathak T. Desulfonylation with Mg-MeOH-NiBr(2): an expedient reagent system for the synthesis of 2-amino-2,3-dideoxy furanosides. Organic Letters. 8: 1303-6. PMID 16562877 DOI: 10.1021/Ol053082A  0.585
2005 Das I, Pathak T, Suresh CG. A diastereoselective and general route to 5-amino-5-deoxysugars: influence of C-3 substitution on the addition of amines to C-5 of vinyl sulfone-modified hex-5-enofuranosyl carbohydrates. The Journal of Organic Chemistry. 70: 8047-54. PMID 16277326 DOI: 10.1021/Jo051143C  0.62
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