Year |
Citation |
Score |
2024 |
Mondal S, Nandi S, Das S, Jana R. A chemoselective hydroxycarbonylation and C-labeling of aryl diazonium salts using formic acid as the C-1 source. Chemical Communications (Cambridge, England). PMID 39495083 DOI: 10.1039/d4cc04758c |
0.467 |
|
2024 |
Varalaxmi K, Pradhan K, Begam HM, Polley A, Kumar D, Jana R. Transition-metal-free iterative two-fold reductive coupling and 1,3-borotropic shift to form 1,4-skipped dienes. Organic & Biomolecular Chemistry. PMID 39378020 DOI: 10.1039/d4ob01389a |
0.774 |
|
2024 |
Das S, Rahaman SA, Pradhan K, Jana R. Organophotoredox-Catalyzed Synthesis of Unnatural α/β Amino Acids and Peptides via Deaminative Three-Component Coupling. Organic Letters. PMID 39137018 DOI: 10.1021/acs.orglett.4c02152 |
0.8 |
|
2024 |
Jana R, Pradhan K. Shining light on the nitro group: distinct reactivity and selectivity. Chemical Communications (Cambridge, England). PMID 39081204 DOI: 10.1039/d4cc02582b |
0.804 |
|
2024 |
Mondal S, Jana R. Green light-mediated dual eosin Y/Pd-catalyzed C(sp)-H arylation of N-H unprotected 2-arylquinazolinones. Organic & Biomolecular Chemistry. PMID 38916115 DOI: 10.1039/d4ob00779d |
0.636 |
|
2023 |
Begam HM, Pradhan K, Varalaxmi K, Jana R. An HFIP-assisted, cobalt-catalyzed three-component electrophilic C-H amination/cyclization/directing group removal cascade to naphtho[1,2-d]imidazoles. Chemical Communications (Cambridge, England). PMID 37078270 DOI: 10.1039/d3cc00749a |
0.804 |
|
2023 |
Manna K, Jana R. Palladium-Catalyzed Cross-Electrophile Coupling between Aryl Diazonium Salt and Aryl Iodide/Diaryliodonium Salt in HO-EtOH. Organic Letters. PMID 36607149 DOI: 10.1021/acs.orglett.2c03932 |
0.618 |
|
2022 |
Nandi S, Mondal S, Jana R. Protocol for chemo- and regioselective C(sp)-H activation using a heterogeneous copper powder-catalyzed reaction. Star Protocols. 3: 101781. PMID 36317172 DOI: 10.1016/j.xpro.2022.101781 |
0.837 |
|
2022 |
Begam HM, Nandi S, Jana R. A directing group switch in copper-catalyzed electrophilic C-H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole. Chemical Science. 13: 5726-5733. PMID 35694354 DOI: 10.1039/d2sc01420c |
0.831 |
|
2022 |
Nandi S, Mondal S, Jana R. Chemo- and regioselective benzylic C(sp)-H oxidation bridging the gap between hetero- and homogeneous copper catalysis. Iscience. 25: 104341. PMID 35602936 DOI: 10.1016/j.isci.2022.104341 |
0.84 |
|
2022 |
Das P, Das S, Jana R. Aryldiazonium Salts and DABSO: A Versatile Combination for Three-Component Sulfonylative Cross-Coupling Reactions. Chemistry, An Asian Journal. e202200085. PMID 35366373 DOI: 10.1002/asia.202200085 |
0.82 |
|
2021 |
Manna K, Ganguly T, Baitalik S, Jana R. Visible-Light- and PPh-Mediated Direct C-N Coupling of Nitroarenes and Boronic Acids at Ambient Temperature. Organic Letters. 23: 8634-8639. PMID 34643396 DOI: 10.1021/acs.orglett.1c03343 |
0.65 |
|
2021 |
Jana R, Begam HM, Dinda E. The emergence of the C-H functionalization strategy in medicinal chemistry and drug discovery. Chemical Communications (Cambridge, England). 57: 10842-10866. PMID 34596175 DOI: 10.1039/d1cc04083a |
0.811 |
|
2021 |
Polley A, Varalaxmi K, Nandi A, Jana R. Divergent Total Synthesis of (±)‐Mahanine and Other Carbazole Alkaloids Asian Journal of Organic Chemistry. 10: 1207-1215. DOI: 10.1002/AJOC.202100176 |
0.585 |
|
2020 |
Manna K, Begam HM, Samanta K, Jana R. Overcoming the Deallylation Problem: Palladium(II)-Catalyzed Chemo-, Regio-, and Stereoselective Allylic Oxidation of Aryl Allyl Ether, Amine, and Amino Acids. Organic Letters. PMID 32955263 DOI: 10.1021/acs.orglett.0c02465 |
0.849 |
|
2020 |
Dinda E, Bhunia SK, Jana R. Palladium-Catalyzed Cascade Reactions for Annulative π -Extension of Indoles to Carbazoles through C–H Bond Activation Current Organic Chemistry. 24: 2612-2633. DOI: 10.2174/1385272824999200817170058 |
0.404 |
|
2020 |
Das P, Das S, Varalaxmi K, Jana R. Metal‐Free, Multicomponent Anti‐Markovnikov Hydroarylsulfonylation and Alkoxyarylsulfonylation of Vinyl Arenes Advanced Synthesis & Catalysis. 363: 575-584. DOI: 10.1002/adsc.202000995 |
0.323 |
|
2019 |
Bhunia SK, Das P, Nandi S, Jana R. Carboxylation of Aryl Triflates with CO Merging Palladium and Visible-Light-Photoredox Catalysts. Organic Letters. PMID 31188621 DOI: 10.1021/acs.orglett.9b01532 |
0.828 |
|
2019 |
Begam HM, Choudhury R, Behera A, Jana R. Copper-Catalyzed Electrophilic Ortho C(sp)-H Amination of Aryl Amines: Dramatic Reactivity of Bicyclic System. Organic Letters. PMID 31184191 DOI: 10.1021/acs.orglett.9b01546 |
0.842 |
|
2019 |
Bairy G, Nandi A, Manna K, Jana R. Ruthenium(II)-Catalyzed Migratory C–H Allylation/Hydroamination Cascade for the Synthesis of Rutaecarpine Analogues Synthesis. 51: 2523-2531. DOI: 10.1055/S-0037-1611525 |
0.662 |
|
2019 |
Das P, Begam HM, Bhunia SK, Jana R. Photoredox‐Catalyzed Tandem Demethylation of
N
,
N
‐Dimethyl Anilines Followed by Amidation with α‐Keto or Alkynyl Carboxylic Acids Advanced Synthesis & Catalysis. 361: 4048-4054. DOI: 10.1002/ADSC.201900525 |
0.773 |
|
2018 |
Polley A, Varalaxmi K, Jana R. Palladium-Catalyzed Ortho C-H Arylation of Aniline Carbamates with Diazonium Salts under Mild Conditions: Expedient Synthesis of Carbazole Alkaloids. Acs Omega. 3: 14503-14516. PMID 31458136 DOI: 10.1021/acsomega.8b02009 |
0.852 |
|
2018 |
Polley A, Varalaxmi K, Jana R. Palladium-Catalyzed Ortho C-H Arylation of Aniline Carbamates with Diazonium Salts under Mild Conditions: Expedient Synthesis of Carbazole Alkaloids. Acs Omega. 3: 14503-14516. PMID 31458136 DOI: 10.1021/acsomega.8b02009 |
0.53 |
|
2018 |
Bhunia SK, Das P, Jana R. Atom-economical selenation of electron-rich arenes and phosphonates with molecular oxygen at room temperature. Organic & Biomolecular Chemistry. PMID 30483684 DOI: 10.1039/c8ob02792g |
0.803 |
|
2018 |
Bairy G, Das S, Begam HM, Jana R. Exceedingly Fast, Direct Access to Dihydroisoquinolino[1,2- b]quinazolinones through a Ruthenium(II)-Catalyzed Redox-Neutral C-H Allylation/Hydroamination Cascade. Organic Letters. PMID 30407020 DOI: 10.1021/acs.orglett.8b03048 |
0.843 |
|
2018 |
Manna MK, Bairy G, Jana R. Sterically Controlled Ru(II)-Catalyzed Divergent Synthesis of 2-Methylindoles and Indolines through a C-H Allylation/Cyclization Cascade. The Journal of Organic Chemistry. PMID 29873230 DOI: 10.1021/acs.joc.8b01034 |
0.861 |
|
2018 |
Das S, Bairy G, Jana R. Ligand-Promoted γ-C(sp)-H Arylation and Unsymmetrical Diarylation to Access Unnatural Amino Acid Derivatives. Organic Letters. PMID 29683681 DOI: 10.1021/acs.orglett.8b00874 |
0.833 |
|
2018 |
Hossian A, Manna K, Das P, Jana R. CuI
/AgI
-Promoted Decarboxylative Alkynylation of ortho-Nitro Benzoic Acids Chemistryselect. 3: 4315-4318. DOI: 10.1002/SLCT.201800758 |
0.558 |
|
2018 |
Polley A, Bairy G, Das P, Jana R. Triple Mode of Alkylation with Ethyl Bromodifluoroacetate:
N
, or
O
‐Difluoromethylation,
N
‐Ethylation and
S
‐(ethoxycarbonyl)difluoromethylation Advanced Synthesis & Catalysis. 360: 4161-4167. DOI: 10.1002/ADSC.201800824 |
0.568 |
|
2017 |
Hossian A, Manna MK, Manna K, Jana R. Palladium-catalyzed decarboxylative, decarbonylative and dehydrogenative C(sp(2))-H acylation at room temperature. Organic & Biomolecular Chemistry. PMID 28749522 DOI: 10.1039/c7ob01466j |
0.847 |
|
2017 |
Manna MK, Bairy G, Jana R. Dual visible-light photoredox and palladium(ii) catalysis for dehydrogenative C2-acylation of indoles at room temperature. Organic & Biomolecular Chemistry. PMID 28682380 DOI: 10.1039/c7ob01418j |
0.808 |
|
2017 |
Manna MK, Bhunia SK, Jana R. Ruthenium(ii)-catalyzed intermolecular synthesis of 2-arylindolines through C-H activation/oxidative cyclization cascade. Chemical Communications (Cambridge, England). PMID 28607985 DOI: 10.1039/c7cc03053c |
0.853 |
|
2017 |
Singh BK, Bairy G, Jana R. A General Copper/Manganese Cocatalyzed C-H Selenation of Arenes, Heteroarenes, and Alkenes under Air Chemistryselect. 2: 9227-9232. DOI: 10.1002/SLCT.201701758 |
0.312 |
|
2016 |
Hossian A, Jana R. Carboxyl radical-assisted 1,5-aryl migration through Smiles rearrangement. Organic & Biomolecular Chemistry. 14: 9768-9779. PMID 27714205 DOI: 10.1039/c6ob01758d |
0.398 |
|
2016 |
Singh BK, Polley A, Jana R. Copper(II)-mediated Intermolecular C(sp2)-H Amination of Benzamides with Electron-Rich Anilines. The Journal of Organic Chemistry. PMID 27148754 DOI: 10.1021/acs.joc.6b00659 |
0.775 |
|
2016 |
Hossian A, Bhunia SK, Jana R. Substrate-Dependent Mechanistic Divergence in Decarboxylative Heck Reaction at Room Temperature. The Journal of Organic Chemistry. 81: 2521-33. PMID 26895388 DOI: 10.1021/acs.joc.6b00100 |
0.748 |
|
2016 |
Singh BK, Jana R. Ligand-Enabled, Copper-Promoted Regio- and Chemoselective Hydroxylation of Arenes, Aryl Halides, and Aryl Methyl Ethers. The Journal of Organic Chemistry. 81: 831-41. PMID 26762789 DOI: 10.1021/acs.joc.5b02302 |
0.574 |
|
2016 |
Hossian A, Bhunia SK, Jana R. Substrate-Dependent Mechanistic Divergence in Decarboxylative Heck Reaction at Room Temperature Journal of Organic Chemistry. 81: 2521-2533. DOI: 10.1021/acs.joc.6b00100 |
0.394 |
|
2015 |
Bhunia SK, Polley A, Natarajan R, Jana R. Through-Space 1,4-Palladium Migration and 1,2-Aryl Shift: Direct Access to Dibenzo[a,c]carbazoles through a Triple CH Functionalization Cascade. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26437569 DOI: 10.1002/chem.201503474 |
0.813 |
|
2015 |
Chaudhari TY, Hossian A, Manna MK, Jana R. Chemo-, regio-, and stereoselective Heck-Matsuda arylation of allylic alcohols under mild conditions. Organic & Biomolecular Chemistry. 13: 4841-5. PMID 25814005 DOI: 10.1039/c5ob00235d |
0.781 |
|
2015 |
Manna MK, Hossian A, Jana R. Merging C-H activation and alkene difunctionalization at room temperature: A palladium-catalyzed divergent synthesis of indoles and indolines Organic Letters. 17: 672-675. PMID 25629624 DOI: 10.1021/ol5036968 |
0.844 |
|
2014 |
Vaden RM, Gligorich KM, Jana R, Sigman MS, Welm BE. The small molecule C-6 is selectively cytotoxic against breast cancer cells and its biological action is characterized by mitochondrial defects and endoplasmic reticulum stress. Breast Cancer Research : Bcr. 16: 472. PMID 25425314 DOI: 10.1186/S13058-014-0472-0 |
0.408 |
|
2014 |
Hossian A, Singha S, Jana R. Palladium(0)-catalyzed intramolecular decarboxylative allylation of ortho nitrobenzoic esters Organic Letters. 16: 3934-3937. PMID 25055344 DOI: 10.1021/ol5017349 |
0.459 |
|
2014 |
Braverman S, Cherkinsky M, Kalendar Y, Jana R, Sprecher M, Goldberg I. Synthesis of water-soluble vinyl selenides and their high glutathione peroxidase (GPx)-like antioxidant activity Synthesis (Germany). 46: 119-125. DOI: 10.1055/S-0033-1338555 |
0.528 |
|
2014 |
Braverman S, Cherkinsky M, Kalendar Y, Jana R, Sprecher M, Goldberg I. ChemInform Abstract: Synthesis of Water-Soluble Vinyl Selenides and Their High Glutathione Peroxidase (GPx)-Like Antioxidant Activity. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201425203 |
0.492 |
|
2013 |
Saini V, Liao L, Wang Q, Jana R, Sigman MS. Pd(0)-catalyzed 1,1-diarylation of ethylene and allylic carbonates. Organic Letters. 15: 5008-11. PMID 24047468 DOI: 10.1021/Ol4023358 |
0.731 |
|
2012 |
Jana R, Pathak TP, Jensen KH, Sigman MS. Palladium(II)-catalyzed enantio- and diastereoselective synthesis of pyrrolidine derivatives. Organic Letters. 14: 4074-7. PMID 22873944 DOI: 10.1021/Ol3016989 |
0.834 |
|
2012 |
Jana R, Pathak TP, Jensen KH, Sigman MS. A Palladium-Catalyzed Enantioselective Hydroamination Route to Pyrrolidines Synfacts. 8: 1068-1068. DOI: 10.1055/S-0032-1317290 |
0.624 |
|
2011 |
Jana R, Tunge JA. A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation. The Journal of Organic Chemistry. 76: 8376-85. PMID 21895010 DOI: 10.1021/Jo201476H |
0.626 |
|
2011 |
Jana R, Partridge JJ, Tunge JA. Migratory decarboxylative coupling of coumarins: synthetic and mechanistic aspects. Angewandte Chemie (International Ed. in English). 50: 5157-61. PMID 21506221 DOI: 10.1002/Anie.201100765 |
0.714 |
|
2011 |
Liao L, Jana R, Urkalan KB, Sigman MS. A palladium-catalyzed three-component cross-coupling of conjugated dienes or terminal alkenes with vinyl triflates and boronic acids. Journal of the American Chemical Society. 133: 5784-7. PMID 21449562 DOI: 10.1021/Ja201358B |
0.825 |
|
2011 |
Jana R, Pathak TP, Sigman MS. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners. Chemical Reviews. 111: 1417-92. PMID 21319862 DOI: 10.1021/Cr100327P |
0.808 |
|
2011 |
Fang J, Jana R, Tunge JA, Subramaniam B. Continuous homogeneous hydroformylation with bulky rhodium catalyst complexes retained by nano-filtration membranes Applied Catalysis a: General. 393: 294-301. DOI: 10.1016/J.Apcata.2010.12.011 |
0.569 |
|
2010 |
Chattopadhyay K, Jana R, Day VW, Douglas JT, Tunge JA. Mechanistic origin of the stereodivergence in decarboxylative allylation. Organic Letters. 12: 3042-5. PMID 20533852 DOI: 10.1021/ol101042x |
0.627 |
|
2010 |
Braverman S, Cherkinsky M, Jana R, Kalendar Y, Sprecher M. Erratum: Reaction of selenium and tellurium halides with propargyl alcohols. The regio‐ and stereoselectivity of addition to the triple bond, Erratum to poc.1729 Journal of Physical Organic Chemistry. 23: 1121-1121. DOI: 10.1002/Poc.1807 |
0.536 |
|
2010 |
Braverman S, Cherkinsky M, Jana R, Kalendar Y, Sprecher M. Reaction of selenium and tellurium halides with propargyl alcohols. the regio- and stereoselectivity of addition to the triple bond Journal of Physical Organic Chemistry. 23: 1114-1120. DOI: 10.1002/Poc.1729 |
0.534 |
|
2009 |
Pahadi NK, Paley M, Jana R, Waetzig SR, Tunge JA. Formation of N-alkylpyrroles via intermolecular redox amination. Journal of the American Chemical Society. 131: 16626-7. PMID 19886656 DOI: 10.1021/Ja907357G |
0.832 |
|
2009 |
Jana R, Trivedi R, Tunge JA. Mild decarboxylative allylation of coumarins. Organic Letters. 11: 3434-6. PMID 19588967 DOI: 10.1021/Ol901288R |
0.675 |
|
2009 |
Duan S, Jana R, Tunge JA. Lewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic esters. The Journal of Organic Chemistry. 74: 4612-4. PMID 19518152 DOI: 10.1021/Jo900367G |
0.653 |
|
2009 |
Jana R, Tunge JA. A homogeneous, recyclable rhodium(I) catalyst for the hydroarylation of Michael acceptors. Organic Letters. 11: 971-4. PMID 19199771 DOI: 10.1021/Ol802927V |
0.576 |
|
2009 |
Ranu BC, Chattopadhyay K, Ghosh S, Jana R. ChemInform Abstract: Ionic Liquid Promoted Regio- and Stereoselective Addition of Thiols to Alkynes and Alkenes under Organic Solvent-Free Condition - A Green Reaction. Cheminform. 40. DOI: 10.1002/CHIN.200942018 |
0.517 |
|
2008 |
Samanta S, Adak L, Jana R, Mostafa G, Tuononen HM, Ranu BC, Goswami S. Oxidative ortho-C-N fusion of aniline by OsO4. Isolation, characterization of oxo-amido Osmium(VI) complexes, and their catalytic activities for oxidative C-C bond cleavage of unsaturated hydrocarbons. Inorganic Chemistry. 47: 11062-70. PMID 18973328 DOI: 10.1021/Ic801352D |
0.554 |
|
2008 |
Ranu BC, Chattopadhyay K, Saha A, Adak L, Jana R, Bhadra S, Dey R, Saha D. Potential of metal nanoparticles in organic reactions Journal of Physics: Conference Series. 106: 012003. DOI: 10.1088/1742-6596/106/1/012003 |
0.446 |
|
2008 |
Ranu BC, Saha A, Jana R. An Efficient Copper Nanoparticle Catalytic System for C-S Bond Formation Synfacts. 2008: 316-316. DOI: 10.1055/S-2008-1042678 |
0.474 |
|
2008 |
Ranu BC, Saha A, Jana R. ChemInform Abstract: Microwave-Assisted Simple and Efficient Ligand-Free Copper Nanoparticle Catalyzed Aryl-Sulfur Bond Formation. Cheminform. 39. DOI: 10.1002/CHIN.200816095 |
0.496 |
|
2008 |
Braverman S, Jana R, Cherkinsky M, Gottlieb HE, Sprecher M. ChemInform Abstract: Regio- and Stereospecific Synthesis of Functionalized Divinyl Selenides. Cheminform. 39. DOI: 10.1002/CHIN.200810197 |
0.538 |
|
2007 |
Ranu BC, Jana R, Sowmiah S. An improved procedure for the three-component synthesis of highly substituted pyridines using ionic liquid. The Journal of Organic Chemistry. 72: 3152-4. PMID 17367198 DOI: 10.1021/Jo070015G |
0.543 |
|
2007 |
Braverman S, Jana R, Cherkinsky M, Gottlieb HE, Sprecher M. Regio- and stereospecific synthesis of functionalized divinyl selenides Synlett. 2663-2666. DOI: 10.1055/S-2007-991051 |
0.545 |
|
2007 |
Ranu BC, Chattopadhyay K, Jana R. Chemo-, regio- and stereoselective addition of triorganoindium reagents to acetates of Baylis–Hillman adducts: a new strategy for the synthesis of (E)- and (Z)-trisubstituted alkenes Tetrahedron Letters. 48: 3847-3850. DOI: 10.1016/J.TETLET.2007.03.154 |
0.511 |
|
2007 |
Ranu BC, Chattopadhyay K, Jana R. Chemo-, Regio- and Stereoselective Addition of Triorganoindium Reagents to Acetates of Baylis—Hillman Adducts: A New Strategy for the Synthesis of (E)- and (Z)-Trisubstituted Alkenes. Cheminform. 38. DOI: 10.1016/J.Tetlet.2007.03.154 |
0.612 |
|
2007 |
Ranu BC, Banerjee S, Jana R. Ionic liquid as catalyst and solvent: the remarkable effect of a basic ionic liquid, [bmIm]OH on Michael addition and alkylation of active methylene compounds Tetrahedron. 63: 776-782. DOI: 10.1016/J.Tet.2006.10.077 |
0.614 |
|
2007 |
Ranu BC, Chattopadhyay K, Jana R. Ionic liquid promoted selective debromination of α-bromoketones under microwave irradiation Tetrahedron. 63: 155-159. DOI: 10.1016/J.TET.2006.10.035 |
0.388 |
|
2007 |
Ranu BC, Chattopadhyay K, Jana R. Ionic Liquid Promoted Selective Debromination of α-Bromoketones under Microwave Irradiation. Cheminform. 38. DOI: 10.1016/J.Tet.2006.10.035 |
0.512 |
|
2007 |
Ranu B, Saha A, Jana R. Microwave-Assisted Simple and Efficient Ligand Free Copper Nanoparticle Catalyzed Aryl-Sulfur Bond Formation Advanced Synthesis & Catalysis. 349: 2690-2696. DOI: 10.1002/Adsc.200700289 |
0.533 |
|
2006 |
Ranu BC, Jana R. Ionic Liquid as Catalyst and Reaction Medium – A Simple, Efficient and Green Procedure for Knoevenagel Condensation of Aliphatic and Aromatic Carbonyl Compounds Using a Task-Specific Basic Ionic Liquid European Journal of Organic Chemistry. 2006: 3767-3770. DOI: 10.1002/EJOC.200600335 |
0.48 |
|
2006 |
Ranu BC, Jana R. Ionic Liquid as Catalyst and Reaction Medium — A Simple, Efficient and Green Procedure for Knoevenagel Condensation of Aliphatic and Aromatic Carbonyl Compounds Using a Task-Specific Basic Ionic Liquid. Cheminform. 37. DOI: 10.1002/Ejoc.200600335 |
0.554 |
|
2005 |
Ranu BC, Jana R. Catalysis by ionic liquid. A green protocol for the stereoselective debromination of vicinal-dibromides by [pmIm]BF4 under microwave irradiation. The Journal of Organic Chemistry. 70: 8621-4. PMID 16209624 DOI: 10.1021/Jo051373R |
0.535 |
|
2005 |
Ranu BC, Jana R. Direct Halogenation of Alcohols and Their Derivatives withtert-Butyl Halides in the Ionic Liquid [pmIm]Br under Sonication Conditions - A Novel, Efficient and Green Methodology European Journal of Organic Chemistry. 2005: 755-758. DOI: 10.1002/EJOC.200400597 |
0.431 |
|
2005 |
Ranu BC, Jana R. Direct Halogenation of Alcohols and Their Derivatives with tert-Butyl Halides in the Ionic Liquid [pmIm]Br under Sonication Conditions — A Novel, Efficient and Green Methodology. Cheminform. 36. DOI: 10.1002/Ejoc.200400597 |
0.438 |
|
2005 |
Ranu B, Jana R. Ionic Liquid as Catalyst and Reaction Medium: A Simple, Convenient and Green Procedure for the Synthesis of Thioethers, Thioesters and Dithianes using an Inexpensive Ionic Liquid, [pmIm]Br Advanced Synthesis & Catalysis. 347: 1811-1818. DOI: 10.1002/Adsc.200505122 |
0.544 |
|
2004 |
Ranu BC, Jana R, Dey SS. An Efficient and Green Synthesis of 2-Arylbenzothiazoles in an Ionic Liquid, [pmIm]Br under Microwave Irradiation. Cheminform. 35. DOI: 10.1246/Cl.2004.274 |
0.466 |
|
2004 |
Ranu BC, Jana R, Dey SS. An Efficient and Green Synthesis of 2-Arylbenzothiazoles in an Ionic Liquid, [pmIm]Br under Microwave Irradiation Chemistry Letters. 33: 274-275. DOI: 10.1246/CL.2004.274 |
0.444 |
|
2004 |
Ranu B, Jana R, Samanta S. A Simple, Efficient and General Procedure for Acetalization of Carbonyl Compounds and Deprotection of Acetals under the Catalysis of Indium(III) Chloride Advanced Synthesis & Catalysis. 346: 446-450. DOI: 10.1002/Adsc.200303154 |
0.731 |
|
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