| Year |
Citation |
Score |
| 2023 |
Zyryanov GV, Kopchuk DS, Kovalev IS, Santra S, Majee A, Ranu BC. Pillararenes as Promising Carriers for Drug Delivery. International Journal of Molecular Sciences. 24. PMID 36982244 DOI: 10.3390/ijms24065167 |
0.461 |
|
| 2021 |
Chatterjee T, Ranu BC. Synthesis of Organosulfur and Related Heterocycles under Mechanochemical Conditions. The Journal of Organic Chemistry. PMID 34351760 DOI: 10.1021/acs.joc.1c01454 |
0.329 |
|
| 2020 |
Ranu BC, Ghosh T, Adak L. Recent Progress on Carbon-chalcogen Bond Formation Reaction Under Microwave Irradiation Current Microwave Chemistry. 7: 40-49. DOI: 10.2174/2213335607666200214130544 |
0.323 |
|
| 2020 |
Egorov IN, Santra S, Kopchuk DS, Kovalev IS, Zyryanov GV, Majee A, Ranu BC, Rusinov VL, Chupakhin ON. Ball milling: an efficient and green approach for asymmetric organic syntheses Green Chemistry. 22: 302-315. DOI: 10.1039/C9Gc03414E |
0.619 |
|
| 2020 |
Egorov IN, Santra S, Kopchuk DS, Kovalev IS, Zyryanov GV, Majee A, Ranu BC, Rusinov VL, Chupakhin ON. Direct Asymmetric Arylation of Imines Advanced Synthesis & Catalysis. DOI: 10.1002/Adsc.202000548 |
0.676 |
|
| 2019 |
Ranu BC, Ghosh T, Jalal S. Recent developments in C-H functionalization via C-H bond activation using ball milling and transition-metal catalysts Arkivoc. 2019: 79-92. DOI: 10.24820/Ark.5550190.P010.862 |
0.385 |
|
| 2019 |
Panja S, Maity S, Majhi B, Ranu BC. Palladium-Catalyzed Olefination of 4H-Benzo[d][1,3]oxazin-4-one Derivatives with Activated Alkenes via Preferential Cyclic Imine-N-Directed Aryl C-H Activation European Journal of Organic Chemistry. 2019: 5777-5786. DOI: 10.1002/Ejoc.201900935 |
0.405 |
|
| 2019 |
Rahman M, Mukherjee A, Kovalev IS, Kopchuk DS, Zyryanov GV, Tsurkan MV, Majee A, Ranu BC, Charushin VN, Chupakhin ON, Santra S. Cover Picture: Recent Advances on Diverse Decarboxylative Reactions of Amino Acids (Adv. Synth. Catal. 10/2019) Advanced Synthesis & Catalysis. 361: 2160-2160. DOI: 10.1002/Adsc.201900451 |
0.734 |
|
| 2019 |
Rahman M, Mukherjee A, Kovalev IS, Kopchuk DS, Zyryanov GV, Tsurkan MV, Majee A, Ranu BC, Charushin VN, Chupakhin ON, Santra S. Recent Advances on Diverse Decarboxylative Reactions of Amino Acids Advanced Synthesis & Catalysis. 361: 2161-2214. DOI: 10.1002/Adsc.201801331 |
0.734 |
|
| 2018 |
Ghosh T, Mukherjee N, Ranu BC. Transition Metal- and Oxidant-Free Base-Mediated Selenation of Bicyclic Arenes at Room Temperature. Acs Omega. 3: 17540-17546. PMID 31458358 DOI: 10.1021/acsomega.8b02740 |
0.417 |
|
| 2018 |
Panja S, Maity P, Ranu BC. Palladium Catalyzed Ligand Free Decarboxylative Coupling of α- Oxocarboxylic Acid with Aryl Diazonium Tetrafluoroborate: An Access to Unsymmetrical Diaryl Ketones. The Journal of Organic Chemistry. PMID 30252459 DOI: 10.1021/Acs.Joc.8B01922 |
0.544 |
|
| 2018 |
Ghosh T, Maity P, Ranu BC. Cu(OAc)2 Promoted ortho C (sp2)-H Amidation of 8-Aminoquinoline Benzamide with Acyl Azide: Selective Formation of Aroyl or Acetyl Amide Based on Catalyst Loading. The Journal of Organic Chemistry. PMID 30211551 DOI: 10.1021/Acs.Joc.8B01654 |
0.47 |
|
| 2018 |
Ghosh T, Maity P, Ranu BC. Cobalt-Catalyzed Remote C-4 Functionalization of 8-Aminoquinoline Amides with Ethers via C-H Activation under Visible-Light Irradiation. Access to α-Heteroarylated Ether Derivatives. Organic Letters. PMID 29384688 DOI: 10.1021/Acs.Orglett.7B03955 |
0.44 |
|
| 2018 |
Maity P, Kundu D, Ghosh T, Ranu BC. Copper catalyzed cyanation through CC bond cleavage of gem-aryl dibromide followed by second cyanation of iodoarene by a released CN unit Organic Chemistry Frontiers. 5: 1586-1599. DOI: 10.1039/C8Qo00108A |
0.469 |
|
| 2018 |
Ghosh T, Maity P, Ranu BC. Cobalt-Copper Catalyzed C(sp2) - N Cross Coupling of Amides or Nitrogenated Heterocycles with Styrenyl or Aryl Halides Chemistryselect. 3: 4406-4412. DOI: 10.1002/SLCT.201800575 |
0.349 |
|
| 2017 |
Maity P, Paroi B, Ranu BC. Transition-Metal-Free Iodine Catalyzed Selenocayanation of Styrenyl Bromides and an Easy Access to Benzoselenophenes via Intermediacy of Styrenyl Selenocyanate. Organic Letters. PMID 29072469 DOI: 10.1021/Acs.Orglett.7B02571 |
0.522 |
|
| 2017 |
Mukherjee N, Maity P, Ghosh T, Panja S, Ranu BC. Visible Light Photocatalyzed Carbon-Heteroatom Bond Formation and Synthesis of Related Compounds Current Green Chemistry. 3: 279-317. DOI: 10.2174/2213346104666170130150016 |
0.307 |
|
| 2017 |
Mukherjee N, Pal S, Saha A, Ranu BC. Silver-catalyzed carbon–selenium cross-coupling using N-(phenylseleno)phthalimide: an alternate approach to the synthesis of organoselenides Canadian Journal of Chemistry. 95: 51-56. DOI: 10.1139/CJC-2016-0427 |
0.391 |
|
| 2017 |
Maity P, Ahammed S, Manna RN, Ranu BC. Calcium mediated C–F bond substitution in fluoroarenes towards C–chalcogen bond formation Organic Chemistry Frontiers. 4: 69-76. DOI: 10.1039/C6Qo00515B |
0.382 |
|
| 2017 |
Panja S, kundu D, Ahammed S, Ranu BC. Highly chemoselective reduction of azides to amines by Fe(0) nanoparticles in water at room temperature Tetrahedron Letters. 58: 3457-3460. DOI: 10.1016/J.Tetlet.2017.07.076 |
0.422 |
|
| 2017 |
Panja S, Maity P, Kundu D, Ranu BC. Iron(0) nanoparticles mediated direct conversion of aryl/heteroaryl amines to chalcogenides via in situ diazotization Tetrahedron Letters. 58: 3441-3445. DOI: 10.1016/J.Tetlet.2017.07.070 |
0.531 |
|
| 2017 |
Maity P, Ranu BC. Iodine-Catalyzed Synthesis of Chalcogenophenes by the Reaction of 1,3-Dienyl Bromides and Potassium Selenocyanate/Potassium Sulfide (KSeCN/K2
S) Advanced Synthesis & Catalysis. 359: 4369-4378. DOI: 10.1002/Adsc.201701232 |
0.532 |
|
| 2017 |
Mukherjee N, Kundu D, Ranu BC. Copper-Silver Dual Catalyzed Decyanative C-Se Cross-Coupling Advanced Synthesis & Catalysis. 359: 329-338. DOI: 10.1002/ADSC.201600933 |
0.308 |
|
| 2016 |
Majhi B, Ranu BC. Palladium-Catalyzed Norbornene-Mediated Tandem ortho-C-H-Amination/ipso-C-I-Cyanation of Iodoarenes: Regiospecific Synthesis of 2-Aminobenzonitrile. Organic Letters. 18: 4162-5. PMID 27551884 DOI: 10.1021/Acs.Orglett.6B02113 |
0.461 |
|
| 2016 |
Ahammed S, Kundu D, Mukherjee N, Ranu B. Microwave Assisted Synthesis of Chalcogenides Current Microwave Chemistry. 4: 25-35. DOI: 10.2174/2213335602666150810204449 |
0.384 |
|
| 2016 |
Ali MH, Olesen B, Ranu B, Clippard L, Heath J, Meyer G, Williams T. Oxidation of Aryl Sulfides to Sulfones with Alumina-Supported Ruthenium Catalyst in Dimethyl Carbonate-Water Media Synthesis (Germany). 48: 429-436. DOI: 10.1055/s-0035-1560834 |
0.327 |
|
| 2016 |
Ghosh T, Maity P, Kundu D, Ranu BC. Cobalt catalysed, copper assisted C(sp2)–P cross coupling New Journal of Chemistry. 40: 9556-9564. DOI: 10.1039/C6Nj02247B |
0.418 |
|
| 2016 |
Ahammed S, Nandi S, Kundu D, Ranu BC. One-pot Suzuki coupling of aromatic amines via visible light photocatalyzed metal free borylation using t-BuONO at room temperature Tetrahedron Letters. DOI: 10.1016/j.tetlet.2016.02.097 |
0.407 |
|
| 2016 |
Ahammed S, Nandi S, Kundu D, Ranu BC. ChemInform Abstract: One-Pot Suzuki Coupling of Aromatic Amines via Visible Light Photocatalyzed Metal Free Borylation Using t-BuONO at Room Temperature. Cheminform. 47. DOI: 10.1002/CHIN.201630217 |
0.304 |
|
| 2016 |
Ali MH, Olesen B, Ranu B, Clippard L, Heath J, Meyer G, Williams T. ChemInform Abstract: Oxidation of Aryl Sulfides to Sulfones with Alumina-Supported Ruthenium Catalyst in Dimethyl Carbonate-Water Media. Cheminform. 47. DOI: 10.1002/CHIN.201624085 |
0.338 |
|
| 2016 |
Majhi B, Kundu D, Ghosh T, Ranu BC. ChemInform Abstract: Palladium-Catalyzed Decarboxylative Selective Acylation of 4H-Benzo[d][1,3]oxazin-4-one Derivatives with α-Oxo Carboxylic Acids via Preferential Cyclic Imine-N-Directed Aryl C-H Activation. Cheminform. 47. DOI: 10.1002/CHIN.201623191 |
0.36 |
|
| 2016 |
Maity P, Kundu D, Ranu BC. ChemInform Abstract: Nickel-Copper-Catalyzed C(sp2)-N Cross-Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201613050 |
0.342 |
|
| 2016 |
Majhi B, Kundu D, Ghosh T, Ranu BC. Palladium-Catalyzed Decarboxylative Selective Acylation of 4H-Benzo[d][1,3]oxazin-4-one Derivatives with α-Oxo Carboxylic acids via Preferential Cyclic Imine-N-Directed Aryl C-H Activation Advanced Synthesis and Catalysis. 358: 283-295. DOI: 10.1002/Adsc.201500786 |
0.473 |
|
| 2015 |
Majhi B, Kundu D, Ranu BC. Ascorbic Acid Promoted Oxidative Arylation of Vinyl Arenes to 2-Aryl Acetophenones without Irradiation at Room Temperature under Aerobic Conditions. The Journal of Organic Chemistry. 80: 7739-45. PMID 26154891 DOI: 10.1021/acs.joc.5b00825 |
0.389 |
|
| 2015 |
Kundu D, Tripathy M, Maity P, Ranu BC. Cobalt-Catalyzed Intermolecular C(sp(2) )O Cross-Coupling. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8727-32. PMID 25926040 DOI: 10.1002/chem.201500058 |
0.406 |
|
| 2015 |
Mukherjee N, Chatterjee T, Ranu BC. Transition metal- and solvent-free synthesis of unsymmetrical diaryl sulfides and selenides under ball-milling Arkivoc. 2016: 53-61. DOI: 10.3998/ark.5550190.p009.238 |
0.456 |
|
| 2015 |
Ahammed S, Kundu D, Siddiqui MN, Ranu BC. Metal and solvent free selective oxidation of sulfides to sulfone using bifunctional ionic liquid [pmim]IO4 Tetrahedron Letters. 56: 335-337. DOI: 10.1016/j.tetlet.2014.11.089 |
0.312 |
|
| 2015 |
Mukherjee N, Chatterjee T, Ranu BC. First Application of Heterogeneous Cobalt Catalysis in Csp2-N Cross-Coupling of Activated Chloroarenes under Ligand-Free Conditions European Journal of Organic Chemistry. 2015: 4018-4023. DOI: 10.1002/ejoc.201500418 |
0.274 |
|
| 2015 |
Maity P, Kundu D, Ranu BC. Visible-light-photocatalyzed metal-free C-H heteroarylation of heteroarenes at room temperature: A sustainable synthesis of biheteroaryls European Journal of Organic Chemistry. 2015: 1727-1734. DOI: 10.1002/ejoc.201500006 |
0.284 |
|
| 2015 |
Mukherjee N, Chatterjee T, Ranu BC. ChemInform Abstract: First Application of Heterogeneous Cobalt Catalysis in Csp2-N Cross-Coupling of Activated Chloroarenes under Ligand-Free Conditions. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201543084 |
0.288 |
|
| 2015 |
Kundu D, Tripathy M, Maity P, Ranu BC. ChemInform Abstract: Cobalt-Catalyzed Intermolecular C(sp2)-O Cross-Coupling. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201543061 |
0.296 |
|
| 2015 |
Maity P, Kundu D, Ranu BC. ChemInform Abstract: Visible-Light-Photocatalyzed Metal-Free C-H Heteroarylation of Heteroarenes at Room Temperature: A Sustainable Synthesis of Biheteroaryls. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201528129 |
0.297 |
|
| 2015 |
Majhi B, Ahammed S, Kundu D, Ranu BC. ChemInform Abstract: Palladium-Catalyzed Oxidative C-C Bond Cleavage of α-Hydroxyketones: Application to C-H Acylation of Azoarenes and Synthesis of a Liver(X) Receptor Agonist. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201527091 |
0.317 |
|
| 2015 |
Ranu BC, Chatterjee T, Mukherjee N. ChemInform Abstract: Carbon-Heteroatom Bond Forming Reactions and Heterocycle Synthesis under Ball Milling Cheminform. 46: no-no. DOI: 10.1002/CHIN.201525284 |
0.404 |
|
| 2015 |
Ahammed S, Kundu D, Siddiqui MN, Ranu BC. ChemInform Abstract: Metal and Solvent Free Selective Oxidation of Sulfides to Sulfone Using Bifunctional Ionic Liquid [pmim]IO4. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201520090 |
0.327 |
|
| 2015 |
Mukherjee N, Kundu D, Ranu BC. ChemInform Abstract: A Co-Operative Ni-Cu System for C(sp)-C(sp) and C(sp)-C(sp2) Cross-Coupling Providing a Direct Access to Unsymmetrical 1,3-Diynes and En-ynes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201516133 |
0.255 |
|
| 2015 |
Ahammed S, Kundu D, Ranu BC. ChemInform Abstract: Cu-Catalyzed Fe-Driven Csp-Cspand Csp-Csp2Cross-Coupling: An Access to 1,3-Diynes and 1,3-Enynes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201507053 |
0.288 |
|
| 2015 |
Majhi B, Ahammed S, Kundu D, Ranu BC. Palladium-Catalyzed Oxidative CC Bond Cleavage of α-Hydroxyketones: Application to CH Acylation of Azoarenes and Synthesis of a Liver(X) Receptor Agonist Asian Journal of Organic Chemistry. 4: 154-163. DOI: 10.1002/Ajoc.201402280 |
0.469 |
|
| 2015 |
Maity P, Kundu D, Ranu BC. Nickel-Copper-Catalyzed C(sp2)- N Cross-Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams Advanced Synthesis and Catalysis. 357: 3617-3626. DOI: 10.1002/adsc.201500457 |
0.332 |
|
| 2014 |
Mukherjee N, Kundu D, Ranu BC. A co-operative Ni-Cu system for Csp-Csp and Csp-Csp(2) cross-coupling providing a direct access to unsymmetrical 1,3-diynes and en-ynes. Chemical Communications (Cambridge, England). 50: 15784-7. PMID 25369787 DOI: 10.1039/C4Cc07413K |
0.439 |
|
| 2014 |
Maity P, Kundu D, Roy R, Ranu BC. A direct synthesis of selenophenes by Cu-catalyzed one-pot addition of a selenium moiety to (E,E)-1,3-dienyl bromides and subsequent nucleophilic cyclization. Organic Letters. 16: 4122-5. PMID 25060565 DOI: 10.1021/Ol501820E |
0.473 |
|
| 2014 |
Ahammed S, Kundu D, Ranu BC. Cu-catalyzed Fe-driven C(sp)-C(sp) and C(s)p-C(sp2) cross-coupling: an access to 1,3-diynes and 1,3-enynes. The Journal of Organic Chemistry. 79: 7391-8. PMID 25046329 DOI: 10.1021/Jo5011069 |
0.493 |
|
| 2014 |
Majhi B, Kundu D, Ahammed S, Ranu BC. tert-Butyl nitrite mediated regiospecific nitration of (E)-azoarenes through palladium-catalyzed directed C-H activation. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9862-6. PMID 25043150 DOI: 10.1002/chem.201403325 |
0.351 |
|
| 2014 |
Chatterjee T, Dey R, Ranu BC. ZnO-supported Pd nanoparticle-catalyzed ligand- and additive-free cyanation of unactivated aryl halides using K4[Fe(CN)6]. The Journal of Organic Chemistry. 79: 5875-9. PMID 24856411 DOI: 10.1021/jo500820q |
0.798 |
|
| 2014 |
Kundu D, Ahammed S, Ranu BC. Visible light photocatalyzed direct conversion of aryl-/heteroarylamines to selenides at room temperature. Organic Letters. 16: 1814-7. PMID 24621272 DOI: 10.1021/ol500567t |
0.427 |
|
| 2014 |
Kundu D, Maity P, Ranu BC. Copper-assisted nickel catalyzed ligand-free C(sp2)-O cross-coupling of vinyl halides and phenols. Organic Letters. 16: 1040-3. PMID 24502267 DOI: 10.1021/ol500134p |
0.385 |
|
| 2014 |
Adimurthy S, Ranu B, Ramachandraiah G, Ganguly B, Ghosh P. Bromide-bromate Couple of Varying Ratios for Bromination, Vicinal Functionalisation and Oxidation in a Clean Manner Current Organic Synthesis. 10: 864-884. DOI: 10.2174/157017941006140206102818 |
0.387 |
|
| 2014 |
Ahammed S, Kundu D, Ranu BC. C(sp)–C(sp) and C(sp)–C(sp2) Cross-Coupling with CuFe2O4 Nanoparticles Synfacts. 10: 1231-1231. DOI: 10.1055/S-0034-1379370 |
0.357 |
|
| 2014 |
Ranu BC, Chatterjee T, Mukherjee N, Maity P, Majhi B. Synthesis of Bioactive Five- and Six-Membered Heterocycles Catalyzed by Heterogeneous Supported Metals Green Synthetic Approaches For Biologically Relevant Heterocycles. 7-43. DOI: 10.1016/B978-0-12-800070-0.00002-5 |
0.372 |
|
| 2014 |
Adimurthy S, Ranu BC, Ramachandraiah G, Ganguly B, Ghosh PK. ChemInform Abstract: Bromide-Bromate Couple of Varying Ratios for Bromination, Vicinal Functionalisation and Oxidation in a Clean Manner Cheminform. 45: no-no. DOI: 10.1002/CHIN.201427256 |
0.305 |
|
| 2014 |
Kundu D, Ranu BC. ChemInform Abstract: Ionic Liquid as Base and Phase Transfer Agent: A Green Protocol for the Synthesis of Diaryl Sulfides in Water. Cheminform. 45: no-no. DOI: 10.1002/chin.201420077 |
0.312 |
|
| 2014 |
Kundu D, Chatterjee T, Ranu BC. ChemInform Abstract: Magnetically Separable CuFe2O4Nanoparticles Catalyzed Ligand-Free C-S Coupling in Water: Access to (E)- and (Z)-Styrenyl-, Heteroaryl and Sterically Hindered Aryl Sulfides. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201409088 |
0.333 |
|
| 2014 |
Majhi B, Kundu D, Ahammed S, Ranu BC. Inside Cover:tert-Butyl Nitrite Mediated Regiospecific Nitration of (E)-Azoarenes through Palladium-Catalyzed Directed CH Activation (Chem. Eur. J. 32/2014) Chemistry - a European Journal. 20: 9818-9818. DOI: 10.1002/Chem.201490133 |
0.422 |
|
| 2013 |
Kundu D, Bhadra S, Mukherjee N, Sreedhar B, Ranu BC. Heterogeneous Cu(II) -catalysed solvent-controlled selective N-arylation of cyclic amides and amines with bromo-iodoarenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 15759-68. PMID 24123356 DOI: 10.1002/chem.201302645 |
0.363 |
|
| 2013 |
Mukherjee N, Chatterjee T, Ranu BC. Reaction under ball-milling: solvent-, ligand-, and metal-free synthesis of unsymmetrical diaryl chalcogenides. The Journal of Organic Chemistry. 78: 11110-4. PMID 24116379 DOI: 10.1021/jo402071b |
0.444 |
|
| 2013 |
Chatterjee T, Ranu BC. Solvent-controlled halo-selective selenylation of aryl halides catalyzed by Cu(II) supported on Al2O3. A general protocol for the synthesis of unsymmetrical organo mono- and bis-selenides. The Journal of Organic Chemistry. 78: 7145-53. PMID 23786642 DOI: 10.1021/jo401062k |
0.466 |
|
| 2013 |
Nagpal L, Haque MM, Saha A, Mukherjee N, Ghosh A, Ranu BC, Stuehr DJ, Panda K. Mechanism of inducible nitric-oxide synthase dimerization inhibition by novel pyrimidine imidazoles. The Journal of Biological Chemistry. 288: 19685-97. PMID 23696643 DOI: 10.1074/Jbc.M112.446542 |
0.469 |
|
| 2013 |
Chatterjee T, Ranu BC. Aerobic oxidation of thiols to disulfides under ball-milling in the absence of any catalyst, solvent, or base Rsc Advances. 3: 10680. DOI: 10.1039/C3Ra41996G |
0.424 |
|
| 2013 |
Kundu D, Mukherjee N, Ranu BC. A general and green procedure for the synthesis of organochalcogenides by CuFe2O4 nanoparticle catalysed coupling of organoboronic acids and dichalcogenides in PEG-400 Rsc Advances. 3: 117-125. DOI: 10.1039/C2Ra22415A |
0.56 |
|
| 2013 |
Mukherjee N, Ahammed S, Bhadra S, Ranu BC. Solvent-free one-pot synthesis of 1,2,3-triazole derivatives by the 'Click' reaction of alkyl halides or aryl boronic acids, sodium azide and terminal alkynes over a Cu/Al2O3 surface under ball-milling Green Chemistry. 15: 389-397. DOI: 10.1039/c2gc36521a |
0.451 |
|
| 2013 |
Ahammed S, Dey R, Ranu BC. Palladium and copper catalyzed one-pot Sonogashira reaction of 2-nitroiodobenzenes with aryl acetylenes and subsequent regioselective hydration in water: synthesis of 2-(2-nitrophenyl)-1-aryl ethanones Tetrahedron Letters. 54: 3697-3701. DOI: 10.1016/J.TETLET.2013.05.021 |
0.461 |
|
| 2013 |
Ghosh S, Dey R, Ahammed S, Ranu BC. Palladium supported on silica gel confined ionic liquid as a reusable catalyst for carbon–carbon cross coupling reaction in water Clean Technologies and Environmental Policy. 16: 1767-1771. DOI: 10.1007/S10098-013-0658-7 |
0.523 |
|
| 2013 |
Ahammed S, Dey R, Ranu BC. ChemInform Abstract: Palladium and Copper Catalyzed One-Pot Sonogashira Reaction of 2-Nitroiodobenzenes with Aryl Acetylenes and Subsequent Regioselective Hydration in Water: Synthesis of 2-(2-Nitrophenyl)-1-aryl Ethanones. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201342076 |
0.467 |
|
| 2013 |
Kundu D, Mukherjee N, Ranu BC. ChemInform Abstract: A General and Green Procedure for the Synthesis of Organochalcogenides by CuFe2O4Nanoparticle Catalyzed Coupling of Organoboronic Acids and Dichalcogenides in PEG-400. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201320210 |
0.402 |
|
| 2013 |
Ahammed S, Bhadra S, Kundu D, Sreedhar B, Ranu BC. ChemInform Abstract: An Efficient and General Procedure for the Synthesis of Alkynyl Chalcogenides (Selenides and Tellurides) by Alumina-Supported Cu(II)-Catalyzed Reaction of Alkynyl Bromides and Diphenyl Dichalcogenides. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201320206 |
0.416 |
|
| 2013 |
Mukherjee N, Ahammed S, Bhadra S, Ranu BC. ChemInform Abstract: Solvent-Free One-Pot Synthesis of 1,2,3-Triazole Derivatives by the “Click” Reaction of Alkyl Halides or Aryl Boronic Acids, Sodium Azide and Terminal Alkynes over a Cu/Al2O3Surface under Ball-Milling. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201319145 |
0.46 |
|
| 2013 |
Kundu D, Chatterjee T, Ranu BC. Magnetically Separable CuFe2O4Nanoparticles Catalyzed Ligand-Free CS Coupling in Water: Access to (E)- and (Z)-Styrenyl-, Heteroaryl and Sterically Hindered Aryl Sulfides Advanced Synthesis & Catalysis. 355: 2285-2296. DOI: 10.1002/Adsc.201300261 |
0.508 |
|
| 2012 |
Saha D, Chatterjee T, Mukherjee M, Ranu BC. Copper(I) hydroxyapatite catalyzed Sonogashira reaction of alkynes with styrenyl bromides. Reaction of cis-styrenyl bromides forming unsymmetric diynes. The Journal of Organic Chemistry. 77: 9379-83. PMID 23025420 DOI: 10.1021/jo3015819 |
0.412 |
|
| 2012 |
Dey R, Mukherjee N, Ahammed S, Ranu BC. Highly selective reduction of nitroarenes by iron(0) nanoparticles in water. Chemical Communications (Cambridge, England). 48: 7982-4. PMID 22531391 DOI: 10.1039/c2cc30999h |
0.78 |
|
| 2012 |
Ranu BC, Dey R, Chatterjee T, Ahammed S. Copper nanoparticle-catalyzed carbon-carbon and carbon-heteroatom bond formation with a greener perspective. Chemsuschem. 5: 22-44. PMID 22213696 DOI: 10.1002/Cssc.201100348 |
0.806 |
|
| 2012 |
Saha D, Adak L, Mukherjee M, Ranu BC. Hydroxyapatite-supported Cu(I)-catalysed cyanation of styrenyl bromides with K4[Fe(CN)6]: an easy access to cinnamonitriles. Organic & Biomolecular Chemistry. 10: 952-7. PMID 22130731 DOI: 10.1039/C1Ob06467C |
0.395 |
|
| 2012 |
Ahammed S, Saha A, Ranu BC. Ruthenium catalysed one-pot synthesis of S-allyl and cinnamyl dithiocarbamates using allyl and cinnamyl acetates in water Rsc Advances. 2: 6329. DOI: 10.1039/C2Ra20856C |
0.546 |
|
| 2012 |
Kundu D, Ahammed S, Ranu BC. Microwave-assisted reaction of aryl diazonium fluoroborate and diaryl dichalcogenides in dimethyl carbonate: a general procedure for the synthesis of unsymmetrical diaryl chalcogenides Green Chemistry. 14: 2024. DOI: 10.1039/C2GC35328H |
0.422 |
|
| 2012 |
Chatterjee T, Saha D, Ranu BC. Solvent-free transesterification in a ball-mill over alumina surface Tetrahedron Letters. 53: 4142-4144. DOI: 10.1016/J.TETLET.2012.05.127 |
0.27 |
|
| 2012 |
Banerjee S, Adak L, Ranu BC. Ionic liquid/PPh3 promoted cleavage of diphenyl disulfide and diselenide: a straight-forward metal-free one-pot route to the synthesis of unsymmetrical sulfides and selenides Tetrahedron Letters. 53: 2149-2152. DOI: 10.1016/J.Tetlet.2012.02.047 |
0.577 |
|
| 2012 |
Dey R, Ranu BC. Palladium-catalyzed site-selective arylation of symmetric dichlorobenzaldehyde to non-symmetric diaryl benzaldehyde via Suzuki coupling Tetrahedron Letters. 53: 1558-1560. DOI: 10.1016/J.Tetlet.2012.01.014 |
0.478 |
|
| 2012 |
Ahammed S, Bhadra S, Kundu D, Sreedhar B, Ranu BC. An efficient and general procedure for the synthesis of alkynyl chalcogenides (selenides and tellurides) by alumina-supported Cu(II)-catalyzed reaction of alkynyl bromides and diphenyl dichalcogenides Tetrahedron. 68: 10542-10549. DOI: 10.1016/j.tet.2012.08.046 |
0.407 |
|
| 2012 |
Nagpal L, Haque MM, Ghosh A, Saha A, Mukherjee N, Ranu BC, Stuehr DJ, Panda K. Mechanism of nitric oxide synthase dimerization inhibition by novel pyrimidine imidazoles Nitric Oxide. 27: S34-S35. DOI: 10.1016/J.Niox.2012.04.123 |
0.524 |
|
| 2012 |
Ahammed S, Saha A, Ranu BC. ChemInform Abstract: Ruthenium-Catalyzed One-Pot Synthesis of S-Allyl and Cinnamyl Dithiocarbamates Using Allyl and Cinnamyl Acetates in Water. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201248043 |
0.416 |
|
| 2012 |
Chatterjee T, Saha D, Ranu BC. ChemInform Abstract: Solvent-Free Transesterification in a Ball-Mill over Alumina Surface. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201247044 |
0.294 |
|
| 2012 |
Kundu D, Ahammed S, Ranu B. ChemInform Abstract: Microwave-Assisted Reaction of Aryl Diazonium Fluoroborate and Diaryl Dichalcogenides in Dimethyl Carbonate: A General Procedure for the Synthesis of Unsymmetrical Diaryl Chalcogenides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201245095 |
0.432 |
|
| 2012 |
Banerjee S, Adak L, Ranu BC. ChemInform Abstract: Ionic Liquid/PPh3Promoted Cleavage of Diphenyl Disulfide and Diselenide: A Straight-Forward Metal-Free One-Pot Route to the Synthesis of Unsymmetrical Sulfides and Selenides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201232197 |
0.391 |
|
| 2012 |
Dey R, Ranu BC. ChemInform Abstract: Palladium-Catalyzed Site-Selective Arylation of Symmetric Dichlorobenzaldehyde to Non-symmetric Diaryl Benzaldehyde via Suzuki Coupling. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201229090 |
0.368 |
|
| 2012 |
Dey R, Ranu BC. ChemInform Abstract: A Convenient and Efficient Protocol for the Synthesis of 4(1H)-Cinnolones, 1,4-Dihydrocinnolines, and Cinnolines in Aqueous Medium: Application for Detection of Nitrite Ions. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201212162 |
0.311 |
|
| 2011 |
Ahammed S, Saha A, Ranu BC. Hydrogenation of azides over copper nanoparticle surface using ammonium formate in water. The Journal of Organic Chemistry. 76: 7235-9. PMID 21793592 DOI: 10.1021/Jo200915H |
0.46 |
|
| 2011 |
Saha A, Ranu BC. Ruthenium(III)-catalysed phenylselenylation of allyl acetates by diphenyl diselenide and indium(I) bromide in neat: isolation and identification of intermediate. Organic & Biomolecular Chemistry. 9: 1763-7. PMID 21258726 DOI: 10.1039/C0Ob00317D |
0.422 |
|
| 2011 |
Ranu BC, Bhadra S, Saha D. Green recyclable supported-metal catalyst for useful organic transformations Current Organic Synthesis. 8: 146-171. DOI: 10.2174/157017911794697312 |
0.482 |
|
| 2011 |
Bhadra S, Adak L, Samanta S, Islam AKMM, Mukherjee M, Ranu BC. Synthesis of Oxazines and Dioxanes from Aziridines and Epoxides Synfacts. 2011: 339-339. DOI: 10.1055/S-0030-1259463 |
0.51 |
|
| 2011 |
Chatterjee T, Bhadra S, Ranu BC. Transition metal-free procedure for the synthesis of S-aryl dithiocarbamates using aryl diazonium fluoroborate in water at room temperature Green Chemistry. 13: 1837-1842. DOI: 10.1039/C1Gc00001B |
0.521 |
|
| 2011 |
Chatterjee T, Dey R, Ranu BC. An easy access to styrenes: trans aryl 1,3-, 1,4- and 1,5-dienes, and 1,3,5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles New Journal of Chemistry. 35: 1103. DOI: 10.1039/C0Nj01019G |
0.513 |
|
| 2011 |
Adak L, Bhadra S, Chattopadhyay K, Ranu BC. Amphiphilic allylation of activated alkenes by allyl acetates and allylstannanes catalyzed by palladium nanoparticles: an easy access to stereodefined substituted cyclohexene derivatives New J. Chem.. 35: 430-437. DOI: 10.1039/C0Nj00624F |
0.54 |
|
| 2011 |
Dey R, Chatterjee T, Ranu BC. Facile cyclization of 2-arylethynyl aniline to 4(1H)-cinnolones: a new chemodosimeter for nitrite ions Tetrahedron Letters. 52: 461-464. DOI: 10.1016/J.Tetlet.2010.11.098 |
0.439 |
|
| 2011 |
Dey R, Ranu BC. A convenient and efficient protocol for the synthesis of 4(1H)-cinnolones, 1,4-dihydrocinnolines, and cinnolines in aqueous medium: application for detection of nitrite ions Tetrahedron. 67: 8918-8924. DOI: 10.1016/J.Tet.2011.09.016 |
0.498 |
|
| 2011 |
Chatterjee T, Bhadra S, Ranu BC. ChemInform Abstract: Transition Metal-Free Procedure for the Synthesis of S-Aryl Dithiocarbamates Using Aryl Diazonium Fluoroborate in Water at Room Temperature. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201144068 |
0.352 |
|
| 2011 |
Chatterjee T, Dey R, Ranu BC. ChemInform Abstract: An Easy Access to Styrenes: trans Aryl 1,3-, 1,4- and 1,5-Dienes, and 1,3,5-Trienes by Hiyama Cross-Coupling Catalyzed by Palladium Nanoparticles. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201138064 |
0.38 |
|
| 2011 |
Adak L, Bhadra S, Chattopadhyay K, Ranu BC. ChemInform Abstract: Amphiphilic Allylation of Activated Alkenes by Allyl Acetates and Allylstannanes Catalyzed by Palladium Nanoparticles: An Easy Access to Stereodefined Substituted Cyclohexene Derivatives. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201126042 |
0.435 |
|
| 2011 |
Dey R, Chatterjee T, Ranu BC. ChemInform Abstract: Facile Cyclization of 2-Arylethynyl Aniline to 4(1H)-Cinnolones: A New Chemodosimeter for Nitrite Ions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201116161 |
0.253 |
|
| 2011 |
Patil RD, Bhadra S, Adimurthy S, Ranu BC. ChemInform Abstract: Green Oxidation of Methylarenes to Benzoic Acids with Bromide/Bromate in Water. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201109074 |
0.274 |
|
| 2011 |
Saha D, Dey R, Ranu BC. ChemInform Abstract: A Simple and Efficient One-Pot Synthesis of Substituted Benzo[b]furans by Sonogashira Coupling-5-endo-dig Cyclization Catalyzed by Palladium Nanoparticles in Water under Ligand- and Copper-Free Aerobic Conditions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201109046 |
0.422 |
|
| 2011 |
Patil RD, Adimurthy S, Ranu BC. ChemInform Abstract: Easy Access to α-Bromoketones and Epoxides from vic-Dibromides under Aqueous Conditions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201109026 |
0.342 |
|
| 2011 |
Saha D, Adak L, Ranu BC. ChemInform Abstract: Palladium(0) Nanoparticle Catalyzed Ligand-Free Direct Arylation of Benzothiazole via C-H Bond Functionalization. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201105122 |
0.345 |
|
| 2010 |
Bhadra S, Adak L, Samanta S, Maidul Islam AK, Mukherjee M, Ranu BC. Alumina-supported Cu(II), a versatile and recyclable catalyst for regioselective ring opening of aziridines and epoxides and subsequent cyclization to functionalized 1,4-benzoxazines and 1,4-benzodioxanes. The Journal of Organic Chemistry. 75: 8533-41. PMID 21070034 DOI: 10.1021/Jo101916E |
0.512 |
|
| 2010 |
Ranu BC, Saha A, Dey R. Using more environmentally friendly solvents and benign catalysts in performing conventional organic reactions. Current Opinion in Drug Discovery & Development. 13: 658-68. PMID 21061229 |
0.809 |
|
| 2010 |
Bhadra S, Saha A, Ranu BC. Al(2)O(3)-supported Cu-Catalyzed Electrophilic Substitution by PhSeBr in Organoboranes, Organosilanes, and Organostannanes. A protocol for the synthesis of unsymmetrical diaryl and alkyl aryl selenides. The Journal of Organic Chemistry. 75: 4864-7. PMID 20560558 DOI: 10.1021/Jo100755G |
0.526 |
|
| 2010 |
Patil RD, Adimurthy S, Ranu BC. Easy Access to α-Bromoketones and Epoxides fromvic-Dibromides Under Aqueous Conditions Synthetic Communications. 40: 3233-3239. DOI: 10.1080/00397910903398643 |
0.422 |
|
| 2010 |
Patil RD, Bhadra S, Adimurthy S, Ranu BC. Green oxidation of methylarenes to benzoic acids with bromide/bromate in water Synthetic Communications. 40: 2922-2929. DOI: 10.1080/00397910903340678 |
0.389 |
|
| 2010 |
Dey R, Sreedhar B, Ranu BC. Suzuki Coupling with Molecular Sieves Supported PalladiumCatalyst Synfacts. 2010: 721-721. DOI: 10.1055/S-0029-1219899 |
0.351 |
|
| 2010 |
Bhadra S, Sreedhar B, Ranu BC. Base-Controlled Sequential C-S Bond Formation byCuSO4/Al2O3 Catalyst Synfacts. 2010: 116-116. DOI: 10.1055/S-0029-1218485 |
0.407 |
|
| 2010 |
Joshi G, Bhadra S, Ghosh S, Agrawal MK, Ganguly B, Adimurthy S, Ghosh PK, Ranu BC. Making Full Use of the Oxidizing Equivalents in Bromate in the Selective Oxidation of Thiols, Sulfides, and Benzylic/Secondary Alcohols into Disulfides, Sulfoxides, and Aldehydes/Ketones Industrial & Engineering Chemistry Research. 49: 1236-1241. DOI: 10.1021/Ie901426T |
0.425 |
|
| 2010 |
Saha D, Adak L, Ranu BC. Palladium(0) nanoparticles-catalyzed ligand-free direct arylation of benzothiazole via C–H bond functionalization Tetrahedron Letters. 51: 5624-5627. DOI: 10.1016/J.Tetlet.2010.08.063 |
0.52 |
|
| 2010 |
Adak L, Bhadra S, Ranu BC. Palladium(0) nanoparticle-catalyzed sp2 C-H activation: A convenient route to alkyl-aryl ketones by direct acylation of aryl bromides and iodides with aldehydes Tetrahedron Letters. 51: 3811-3814. DOI: 10.1016/j.tetlet.2010.05.067 |
0.459 |
|
| 2010 |
Saha A, Ranu BC. Transition metal-free activation of allylic acetates toward regioselective S-allylation of thiols Tetrahedron Letters. 51: 1902-1905. DOI: 10.1016/J.Tetlet.2010.02.015 |
0.436 |
|
| 2010 |
Dey R, Sreedhar B, Ranu BC. Molecular sieves-supported palladium(II) catalyst: Suzuki coupling of chloroarenes and an easy access to useful intermediates for the synthesis of irbesartan, losartan and boscalid Tetrahedron. 66: 2301-2305. DOI: 10.1016/J.Tet.2010.02.011 |
0.509 |
|
| 2010 |
Saha D, Dey R, Ranu BC. A Simple and Efficient One-Pot Synthesis of Substituted Benzo[b]furans by Sonogashira Coupling-5-endo-dig Cyclization Catalyzed by Palladium Nanoparticles in Water Under Ligand- and Copper-Free Aerobic Conditions European Journal of Organic Chemistry. 2010: 6067-6071. DOI: 10.1002/Ejoc.201000980 |
0.554 |
|
| 2010 |
Adak L, Bhadra S, Ranu BC. ChemInform Abstract: Palladium(0) Nanoparticle Catalyzed sp2 C-H Activation: A Convenient Route to Alkyl-Aryl Ketones by Direct Acylation of Aryl Bromides and Iodides with Aldehydes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201045064 |
0.428 |
|
| 2010 |
Dey R, Sreedhar B, Ranu BC. ChemInform Abstract: Molecular Sieves-Supported Palladium(I) Catalyst: Suzuki Coupling of Chloroarenes and an Easy Access to Useful Intermediates for the Synthesis of Irbesartan, Losartan and Boscalid. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201032098 |
0.393 |
|
| 2010 |
Saha A, Ranu BC. ChemInform Abstract: Transition Metal Free Activation of Allylic Acetates Toward Regioselective S-Allylation of Thiols. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201029089 |
0.325 |
|
| 2010 |
Ranu BC, Chattopadhyay K, Adak L, Saha A, Bhadra S, Dey R, Saha D. ChemInform Abstract: Metal Nanoparticles as Efficient Catalysts for Organic Reactions Cheminform. 41: no-no. DOI: 10.1002/CHIN.201023233 |
0.4 |
|
| 2010 |
Bhadra S, Ranu BC. ChemInform Abstract: Water-Promoted Regioselective Hydrothiolation of Alkynes. Cheminform. 41. DOI: 10.1002/CHIN.201016034 |
0.291 |
|
| 2010 |
Bhadra S, Sreedhar B, Ranu BC. ChemInform Abstract: Recyclable Heterogeneous Supported Copper-Catalyzed Coupling of Thiols with Aryl Halides: Base-Controlled Differential Arylthiolation of Bromoiodobenzenes. Cheminform. 41. DOI: 10.1002/CHIN.201007069 |
0.358 |
|
| 2010 |
Ranu BC, Samanta S. ChemInform Abstract: Use of Indium Hydride (Cl2InH) for Chemoselective Reduction of the Carbon-Carbon Double Bond in Conjugated Alkenes. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200252047 |
0.621 |
|
| 2010 |
Ranu BC, Samanta S, Das A. ChemInform Abstract: Reduction of Trihalomethyl Carbinols and Their Acetates Mesylates and Tosylates by Indium Metal. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200245070 |
0.628 |
|
| 2010 |
Ranu BC, Samanta S, Hajra A. ChemInform Abstract: Unusual Cleavage of Ethers by Thiophenol on the Surface of Silica Gel Impregnated with Indium(III) Chloride under Microwave Irradiation: Efficient Procedure for the Synthesis of Thioethers Through Transthioetherification. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200238081 |
0.745 |
|
| 2010 |
Ranu BC, Das A, Samanta S. ChemInform Abstract: Highly Efficient Transthioacetalization of O,O-Acetals Catalyzed by Indium(III) Chloride. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200236063 |
0.275 |
|
| 2010 |
Ranu BC, Dey SS, Hajra A. ChemInform Abstract: Indium Trichloride Catalyzed One-Step Synthesis of α-Amino Nitriles by a Three-Component Condensation of Carbonyl Compounds, Amines and Potassium Cyanide. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200232055 |
0.623 |
|
| 2010 |
Ranu BC, Samanta S, Guchhait SK. ChemInform Abstract: Zinc Tetrafluoroborate Catalyzed Mannich-Type Reaction of Aldimines and Silyl Enol Ethers in Aqueous Medium. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200228077 |
0.701 |
|
| 2010 |
Ranu BC, Samanta S, Hajra A. ChemInform Abstract: Indium-Mediated Allylation of β-Keto Phosphonates. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200215178 |
0.712 |
|
| 2010 |
Ranu B, Hajra A. ChemInform Abstract: Highly Selective One-Pot Conversion of THP and MOM Ethers to Acetates by Indium Triiodide-Catalyzed Deprotection and Subsequent Transesterification by Ethyl Acetate. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200209076 |
0.647 |
|
| 2010 |
Ranu BC, Dutta J, Guchhait SK. ChemInform Abstract: Selective Reduction of Terminal Alkynes to Alkenes by Indium Metal. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200149037 |
0.334 |
|
| 2010 |
Ranu BC, Dutta J, Guchhait SK. ChemInform Abstract: Indium Metal as a Reducing Agent. Selective Reduction of the Carbon-Carbon Double Bond in Highly Activated Conjugated Alkenes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200149036 |
0.306 |
|
| 2010 |
Ranu BC, Samanta S, Guchhait SK. ChemInform Abstract: Stereoselective Reduction of Aryl-Substituted gem-Dibromides to Vinyl Bromides by Indium Metal. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200142104 |
0.685 |
|
| 2010 |
Ranu BC, Hajra A. ChemInform Abstract: Synthesis of Alkyl-Substituted Pyrroles by Three-Component Coupling of Carbonyl Compound, Amine and Nitro-Alkane/Alkene on a Solid Surface of Silica Gel/Alumina under Microwave Irradiation. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200140107 |
0.619 |
|
| 2010 |
Ranu BC, Hajra A. ChemInform Abstract: Indium Triiodide Catalyzed One-Step Conversion of Tetrahydropyranyl Ethers to Acetates with High Selectivity. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200125069 |
0.617 |
|
| 2010 |
Ranu BC, Hajra A, Jana U. ChemInform Abstract: Microwave-Assisted Simple Synthesis of Quinolines from Anilines and Alkyl Vinyl Ketones on the Surface of Silica Gel in the Presence of Indium(III) Chloride. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200017139 |
0.632 |
|
| 2010 |
Ranu BC, Hajra A, Jana U. ChemInform Abstract: Microwave-Assisted Synthesis of Substituted Pyrroles by a Three-Component Coupling of α,β-Unsaturated Carbonyl Compounds, Amines, and Nitroalkanes on the Surface of Silica Gel. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200017117 |
0.609 |
|
| 2010 |
Ranu BC, Hajra A, Jana U. ChemInform Abstract: General Procedure for the Synthesis of α-Amino Phosphonates from Aldehydes and Ketones Using Indium(III) Chloride as a Catalyst. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200003168 |
0.63 |
|
| 2010 |
Ranu BC, Sarkar A, Guchhait SK, Ghosh K. ChemInform Abstract: Catalytic Hydrogen Transfer Reductions Using Ammonium Formate Cheminform. 30: no-no. DOI: 10.1002/CHIN.199949227 |
0.314 |
|
| 2010 |
Ranu BC, Dutta P, Sarkar A. ChemInform Abstract: Indium as a Reducing Agent. Chemoselective Reduction of α-Halocarbonyl Compounds and Benzyl Halides by Indium Metal in Water under Sonication. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199938067 |
0.336 |
|
| 2010 |
Ranu BC, Jana U, Majee A. ChemInform Abstract: A Simple and Efficient Method for Selective Deprotection of t-Butyldimethylsilyl Ethers by Zinc Tetrafluoroborate in Water. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199923087 |
0.579 |
|
| 2010 |
Ranu BC, Jana U. ChemInform Abstract: Indium(III) Chloride-Promoted Rearrangement of Epoxides: A Selective Synthesis of Substituted Benzylic Aldehydes and Ketones. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199914046 |
0.469 |
|
| 2010 |
Ranu BC, Dutta P, Sarkar A. ChemInform Abstract: Indium Promoted Reductive Homocoupling of Alkyl and Aryl Halides. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199910065 |
0.438 |
|
| 2010 |
Majee A, Das AR, Ranu BC. ChemInform Abstract: Zinc Mediated Allylation of Aldehydes and Ketones Using Allyl Bromides and Commercial Zinc Dust. The Issue of Regio- and Stereoselectivity. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199909043 |
0.663 |
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| 2010 |
RANU BC, GUCHHAIT SK, SARKAR A. ChemInform Abstract: Stereoselective Debromination of Aryl-Substituted vic-Dibromide with Indium Metal. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199901067 |
0.375 |
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| 2010 |
RANU BC, GUCHHAIT SK, GHOSH K. ChemInform Abstract: Chemoselective Hydrogenation of α,β-Unsaturated Sulfones and Phosphonates via Palladium-Assisted Hydrogen Transfer by Ammonium Formate. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199850057 |
0.333 |
|
| 2010 |
AVALOS M, BABIANO R, BRAVO JL, CINTAS P, JIMENEZ JL, PALACIOS JC, RANU BC. ChemInform Abstract: Cycloadditions with Clays and Alumina without Solvents. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199828048 |
0.37 |
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| 2010 |
RANU BC, MAJEE A, SARKAR A. ChemInform Abstract: One-Pot Reductive Amination of Conjugated Aldehydes and Ketones with Silica Gel and Zinc Borohydride. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199823056 |
0.675 |
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| 2010 |
RANU BC, SAHA M, BHAR S. ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 9. A Convenient Procedure for Aldol Reaction of Ketene Silyl Acetals with Aldehydes on the Solid Surface of Alumina. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199747069 |
0.386 |
|
| 2010 |
RANU BC, SARKAR A, MAJEE A. ChemInform Abstract: Reduction of Imines with Zinc Borohydride Supported on Silica Gel. Highly Stereoselective Synthesis of Substituted Cyclohexylamines. Cheminform. 28: no-no. DOI: 10.1002/chin.199730054 |
0.457 |
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| 2010 |
RANU BC, SAHA M, BHAR S. ChemInform Abstract: Microwave-Assisted Michael Addition of Cycloalkenones and Substituted Enones on the Surface of Alumina in Dry Media. Cheminform. 28: no-no. DOI: 10.1002/chin.199726066 |
0.336 |
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| 2010 |
RANU BC, GHOSH K, JANA U. ChemInform Abstract: Simple and Improved Procedure for Regioselective Acylation of Aromatic Ethers with Carboxylic Acids on the Solid Surface of Alumina in the Presence of Trifluoroacetic Anhydride. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199719087 |
0.385 |
|
| 2010 |
RANU BC, BHAR S. ChemInform Abstract: Dealkylation of Ethers. A Review Cheminform. 27: no-no. DOI: 10.1002/chin.199649307 |
0.248 |
|
| 2010 |
RANU BC, BHAR S, PATRA A, NAYAK NP, MUKHERJEE M. ChemInform Abstract: Rearrangement of Dithianylcyclobutachromanol Derivatives to 1,2,2a,8,9, 9a-Hexahydrocyclobuta(b)(1)benzoxepin-8,9-dione. Cheminform. 27: no-no. DOI: 10.1002/chin.199648061 |
0.228 |
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| 2010 |
RANU BC, MAJEE A, DAS AR. ChemInform Abstract: A Convenient Synthesis of β,γ-Unsaturated Ketones Through Zinc-Mediated Allylation of Acid Chlorides. Cheminform. 27: no-no. DOI: 10.1002/chin.199622078 |
0.649 |
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| 2010 |
RANU BC, MAJEE A, DAS AR. ChemInform Abstract: Facile and Efficient Synthesis of Homoallylic Alcohols Using Allyl Bromide and Commercial Zinc Dust. Cheminform. 26: no-no. DOI: 10.1002/chin.199548051 |
0.37 |
|
| 2010 |
RANU BC, SAHA M. ChemInform Abstract: A Simple, Efficient, and Selective Method for Tetrahydropyranylation of Alcohols on a Solid Phase of Alumina Impregnated with Zinc Chloride. Cheminform. 26: no-no. DOI: 10.1002/chin.199535088 |
0.325 |
|
| 2010 |
BHAR S, RANU BC. ChemInform Abstract: Zinc-Promoted Selective Cleavage of Ethers in Presence of Acyl Chloride. Cheminform. 26: no-no. DOI: 10.1002/chin.199530034 |
0.377 |
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| 2010 |
RANU BC, MAJEE A, DAS AR. ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 7. A Simple and Convenient Procedure for the Methoxymethylation of Alcohols with Methoxymethyl Chloride on the Surface of Alumina. Cheminform. 26: no-no. DOI: 10.1002/chin.199525077 |
0.601 |
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| 2010 |
RANU BC, BHAR S, CHAKRABORTY R, DAS AR, SAHA M, SARKAR A, CHAKRABORTI R, SARKAR DC. ChemInform Abstract: Surface-Mediated Reaction - A Powerful Technique in Organic Synthesis. Use of Alumina and Silica Gel as Active Surface for Useful Synthetic Transformations Cheminform. 26: no-no. DOI: 10.1002/chin.199519260 |
0.344 |
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| 2010 |
RANU BC, SARKAR A, CHAKRABORTY R. ChemInform Abstract: Reduction of Azides with Zinc Borohydride. Cheminform. 26: no-no. DOI: 10.1002/chin.199504091 |
0.339 |
|
| 2010 |
RANU BC, SAHA M, BHAR S. ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 6. Mukaiyama-Michael Addition of Silyl Enol Ethers to Alkyl Vinyl Ketones on the Surface of Alumina: A Simple and Convenient Method for the Synthesis of 1,5- Diketones. Cheminform. 26: no-no. DOI: 10.1002/chin.199501056 |
0.419 |
|
| 2010 |
RANU BC, SARKAR A, SAHA M, CHAKRABORTY R. ChemInform Abstract: Silica Gel Supported Zinc Borohydride. Part 4. A Novel Reagent for the Hydration of Unactivated Alkenes and Alkynes. Cheminform. 25: no-no. DOI: 10.1002/chin.199441075 |
0.397 |
|
| 2010 |
RANU BC, DAS AR. ChemInform Abstract: Two-Carbon Ring Expansion Through Free Cyclobutylcarbinyl Radical Fragmentation. Cheminform. 25: no-no. DOI: 10.1002/chin.199433058 |
0.276 |
|
| 2010 |
RANU BC, CHAKRABORTY R. ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 5. Aldol Reaction of Silyl Enol Ethers with Aldehydes on a Solid Surface of Neutral Alumina: Selectivity for anti Aldols. Cheminform. 24: no-no. DOI: 10.1002/chin.199343068 |
0.385 |
|
| 2010 |
RANU BC, CHAKRABORTY R, SAHA M. ChemInform Abstract: An Unusual Regioselective Anti-Markovnikov Hydration of Alkenes with Zinc Borohydride on Silica Gel Support. Cheminform. 24: no-no. DOI: 10.1002/chin.199341140 |
0.333 |
|
| 2010 |
RANU BC, SAHA M, BHAR S. ChemInform Abstract: Surface-Mediated Solid Phase Reactions. Mukaiyama-Michael Addition of Silyl Enol Ethers to Methyl Vinyl Ketone on the Surface of Alumina. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199333056 |
0.37 |
|
| 2010 |
RANU BC, BHAR S, CHAKRABORTI R. ChemInform Abstract: Synthesis of β-Keto 1,3-Dithianes from Acetylenic Ketones. Cheminform. 24: no-no. DOI: 10.1002/chin.199320227 |
0.382 |
|
| 2010 |
CHAKRABORTY R, DAS AR, RANU BC. ChemInform Abstract: Ion Exchange Resin-Mediated Hydrolytic Cleavage of α-Nitro Epoxides. Simple One-Pot Synthesis of α-Hydroxy Ketones. Cheminform. 24: no-no. DOI: 10.1002/chin.199301084 |
0.373 |
|
| 2010 |
RANU BC, DAS AR. ChemInform Abstract: Silica Gel-Supported Zinc Borohydride. Part 3. Regioselective Reductive Cleavage of Methylenecycloalkane Oxides to the Less- Substituted Alcohols. Cheminform. 23: no-no. DOI: 10.1002/chin.199248084 |
0.333 |
|
| 2010 |
RANU BC, DAS AR. ChemInform Abstract: Highly Selective Reduction of 2-Nitrocycloalkanones (I) to 2- Nitrocycloalkanols (II) with Zinc Borohydride in DME. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199243109 |
0.291 |
|
| 2010 |
RANU BC, CHAKRABORTY R. ChemInform Abstract: Reduction of Conjugated Nitroalkenes with Zinc Borohydride. A Mild Method for Converting Monosubstituted Nitroalkenes to Nitroalkanes and Disubstituted Ones to Oximes. Cheminform. 23: no-no. DOI: 10.1002/chin.199241072 |
0.369 |
|
| 2010 |
RANU BC, SARKAR DC, CHAKRABORTY R. ChemInform Abstract: A Simple and Improved Procedure for Selective Ring Bromination of Alkyl-Substituted Aromatic Hydrocarbons on the Surface of Alumina. Cheminform. 23: no-no. DOI: 10.1002/chin.199238090 |
0.39 |
|
| 2010 |
RANU BC, BHAR S. ChemInform Abstract: Surface-Mediated Solid Phase Reaction: Dramatic Improvement of Michael Reaction on the Surface of Alumina. Cheminform. 23: no-no. DOI: 10.1002/chin.199221076 |
0.346 |
|
| 2010 |
RANU BC, BASU MK. ChemInform Abstract: Stereocontrolled Construction of Angularly Functionalized trans-Fused Cycloheptanoids via α-Hydroxycyclobutane Rearrangement Followed by Retroaldol Cleavage. Cheminform. 23: no-no. DOI: 10.1002/chin.199219130 |
0.324 |
|
| 2010 |
RANU BC, BHAR S. ChemInform Abstract: Surface-Mediated Solid-Phase Reaction. Part 2. Highly Selective Monoand Di-C-alkylation of 1,3-Dicarbonyl Compounds on the Surface of Alumina. Cheminform. 23: no-no. DOI: 10.1002/chin.199219111 |
0.352 |
|
| 2010 |
RANU BC, CHAKRABORTY R. ChemInform Abstract: Highly Selective Reduction of Conjugated Nitroalkenes with Zinc Borohydride in DME. Cheminform. 23: no-no. DOI: 10.1002/chin.199216118 |
0.35 |
|
| 2010 |
RANU BC, CHAKRABORTY R. ChemInform Abstract: Chemoselective Reduction of Aldehydes with Zinc Borohydride in Tetrahydrofuran. Cheminform. 23: no-no. DOI: 10.1002/chin.199215096 |
0.413 |
|
| 2010 |
RANU BC, BHAR S, SARKAR DC. ChemInform Abstract: Surface-Mediated Solid Phase Michael Reaction: Dramatic Acceleration on Alumina. Cheminform. 23: no-no. DOI: 10.1002/chin.199213151 |
0.341 |
|
| 2010 |
RANU BC, CHAKRABORTY R, SARKAR DC. ChemInform Abstract: A Novel Chiral Auxiliary for Enantioselective Synthesis of Tertiary Alcohol. Cheminform. 23: no-no. DOI: 10.1002/chin.199211057 |
0.364 |
|
| 2010 |
RANU BC, DAS AR. ChemInform Abstract: Silica Gel Supported Zinc Borohydride. Part 2. Regioselective 1,2- Reduction of Conjugated Ketones and Aldehydes to the Corresponding Allylic Alcohols. Cheminform. 22: no-no. DOI: 10.1002/chin.199152104 |
0.379 |
|
| 2010 |
RANU BC, DAS AR. ChemInform Abstract: Regio- and Stereoselective Reductive Cleavage of Epoxides with Zinc Borohydride Supported on Silica Gel. Cheminform. 22: no-no. DOI: 10.1002/chin.199113111 |
0.395 |
|
| 2010 |
RANU BC, CHAKRABORTY R. ChemInform Abstract: Ion Exchange Resin-Mediated Hydrolytic Cleavage of Epoxides. Simple One-Pot Synthesis of 2-Aryl Ketones from 1-Aryl-1,2-epoxides. Cheminform. 22: no-no. DOI: 10.1002/chin.199109077 |
0.426 |
|
| 2009 |
Adak L, Chattopadhyay K, Ranu BC. Palladium nanoparticle-catalyzed C-N bond formation. A highly regio- and stereoselective allylic amination by allyl acetates. The Journal of Organic Chemistry. 74: 3982-5. PMID 19382763 DOI: 10.1021/Jo9003037 |
0.532 |
|
| 2009 |
Saha A, Saha D, Ranu BC. Copper nano-catalyst: sustainable phenyl-selenylation of aryl iodides and vinyl bromides in water under ligand free conditions. Organic & Biomolecular Chemistry. 7: 1652-7. PMID 19343253 DOI: 10.1039/B819137A |
0.531 |
|
| 2009 |
Ranu BC, Chattopadhyay K, Adak L, Saha A, Bhadra S, Dey R, Saha D. Metal nanoparticles as efficient catalysts for organic reactions Pure and Applied Chemistry. 81: 2337-2354. DOI: 10.1351/Pac-Con-08-11-19 |
0.552 |
|
| 2009 |
Bhadra S, Ranu BC. Water-promoted regioselective hydrothiolation of alkynes Canadian Journal of Chemistry. 87: 1605-1609. DOI: 10.1139/V09-130 |
0.416 |
|
| 2009 |
Adak L, Chattopadhyay K, Ranu BC. C-N Bond Formation with Palladium Nanoparticles Synfacts. 2009: 937-937. DOI: 10.1055/S-0029-1217500 |
0.385 |
|
| 2009 |
Chattopadhyay K, Dey R, Ranu BC. Suzuki Coupling and Cyanation with CuO/Pd Synfacts. 2009: 933-933. DOI: 10.1055/S-0029-1217497 |
0.342 |
|
| 2009 |
Ranu B, Dey R, Chattopadhyay K. Pd Nanoparticle Catalyzed Allyl Cross-Coupling of Siloxanes Synfacts. 2009: 0321-0321. DOI: 10.1055/S-0028-1087713 |
0.39 |
|
| 2009 |
Saha D, Saha A, Ranu BC. Remarkable influence of substituent in ionic liquid in control of reaction: Simple, efficient and hazardous organic solvent free procedure for the synthesis of 2-aryl benzimidazoles promoted by ionic liquid, [pmim]BF 4 Green Chemistry. 11: 733-737. DOI: 10.1039/b823543k |
0.431 |
|
| 2009 |
Saha D, Saha A, Ranu BC. Ionic liquid-promoted dehydration of aldoximes: a convenient access to aromatic, heteroaromatic and aliphatic nitriles Tetrahedron Letters. 50: 6088-6091. DOI: 10.1016/J.Tetlet.2009.08.069 |
0.482 |
|
| 2009 |
Ghosh S, Dey R, Chattopadhyay K, Ranu BC. Water-promoted highly regio- and stereoselective synthesis of α-dehydro-β-amino esters and nitriles from Baylis–Hillman acetates Tetrahedron Letters. 50: 4892-4895. DOI: 10.1016/J.Tetlet.2009.06.051 |
0.542 |
|
| 2009 |
Patil RD, Joshi G, Adimurthy S, Ranu BC. Facile one-pot synthesis of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent Tetrahedron Letters. 50: 2529-2532. DOI: 10.1016/J.Tetlet.2009.03.047 |
0.473 |
|
| 2009 |
Chattopadhyay K, Dey R, Ranu BC. Shape-dependent catalytic activity of copper oxide-supported Pd(0) nanoparticles for Suzuki and cyanation reactions Tetrahedron Letters. 50: 3164-3167. DOI: 10.1016/J.Tetlet.2009.01.027 |
0.463 |
|
| 2009 |
Saha D, Chattopadhyay K, Ranu BC. Aerobic ligand-free Suzuki coupling catalyzed by in situ-generated palladium nanoparticles in water Tetrahedron Letters. 50: 1003-1006. DOI: 10.1016/J.Tetlet.2008.12.063 |
0.516 |
|
| 2009 |
Ranu BC, Saha A, Mandal T. An indium–TMSCl promoted reaction of diphenyl diselenide and diorganyl disulfides with aldehydes: novel routes to selenoacetals, thioacetals and alkyl phenyl selenides Tetrahedron. 65: 2072-2078. DOI: 10.1016/J.Tet.2008.12.079 |
0.547 |
|
| 2009 |
Ghosh S, Dey R, Chattopadhyay K, Ranu BC. ChemInform Abstract: Water-Promoted Highly Regio- and Stereoselective Synthesis of α-Dehydro-β-amino Esters and Nitriles from BaylisâHillman Acetates. Cheminform. 40. DOI: 10.1002/CHIN.200949061 |
0.4 |
|
| 2009 |
Saha D, Saha A, Ranu BC. ChemInform Abstract: Remarkable Influence of Substituent in Ionic Liquid in Control of Reaction: Simple, Efficient and Hazardous Organic Solvent Free Procedure for the Synthesis of 2-Aryl Benzimidazoles Promoted by Ionic Liquid, [pmim]BF4. Cheminform. 40. DOI: 10.1002/chin.200942129 |
0.427 |
|
| 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 |
0.693 |
|
| 2009 |
Chattopadhyay K, Dey R, Ranu BC. ChemInform Abstract: Shape-Dependent Catalytic Activity of Copper Oxide-Supported Pd(0) Nanoparticles for Suzuki and Cyanation Reactions. Cheminform. 40. DOI: 10.1002/chin.200941084 |
0.344 |
|
| 2009 |
Patil RD, Joshi G, Adimurthy S, Ranu BC. ChemInform Abstract: Facile One-Pot Synthesis of α-Bromoketones from Olefins Using Bromide/Bromate Couple as a Nonhazardous Brominating Agent. Cheminform. 40. DOI: 10.1002/chin.200935070 |
0.4 |
|
| 2009 |
Ranu BC, Saha A, Mandal T. ChemInform Abstract: An Indium-TMSCl Promoted Reaction of Diphenyl Diselenide and Diorganyl Disulfides with Aldehydes: Novel Routes to Selenoacetals, Thioacetals and Alkyl Phenyl Selenides. Cheminform. 40. DOI: 10.1002/chin.200927172 |
0.463 |
|
| 2009 |
Saha D, Chattopadhyay K, Ranu BC. ChemInform Abstract: Aerobic Ligand-Free Suzuki Coupling Catalyzed by in situ Generated Palladium Nanopaticles in Water. Cheminform. 40. DOI: 10.1002/chin.200923088 |
0.334 |
|
| 2009 |
Bhadra S, Saha A, Ranu BC. ChemInform Abstract: One-Pot Copper Nanoparticle Catalyzed Synthesis of S-Aryl- and S-Vinyl Dithiocarbamates in Water: High Diastereoselectivity Achieved for Vinyl Dithiocarbamates. Cheminform. 40. DOI: 10.1002/CHIN.200912093 |
0.388 |
|
| 2009 |
Saha A, Ranu B. ChemInform Abstract: Highly Chemoselective Reduction of Aromatic Nitro Compounds by Copper Nanoparticles/Ammonium Formate. Cheminform. 40. DOI: 10.1002/CHIN.200903063 |
0.344 |
|
| 2009 |
Bhadra S, Sreedhar B, Ranu BC. Recyclable heterogeneous supported copper-catalyzed coupling of thiols with aryl halides: base-controlled differential arylthiolation of bromoiodobenzenes Advanced Synthesis and Catalysis. 351: 2369-2378. DOI: 10.1002/Adsc.200900358 |
0.504 |
|
| 2008 |
Dey R, Chattopadhyay K, Ranu BC. Palladium(0) nanoparticle catalyzed cross-coupling of allyl acetates and aryl and vinyl siloxanes. The Journal of Organic Chemistry. 73: 9461-4. PMID 18998730 DOI: 10.1021/Jo802214M |
0.806 |
|
| 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 |
0.677 |
|
| 2008 |
Saha A, Ranu B. Highly chemoselective reduction of aromatic nitro compounds by copper nanoparticles/ammonium formate. The Journal of Organic Chemistry. 73: 6867-70. PMID 18656983 DOI: 10.1021/Jo800863M |
0.497 |
|
| 2008 |
Ranu BC, Adak L, Chattopadhyay K. Hydroxyapatite-supported palladium-catalyzed efficient synthesis of (E)-2-alkene-4-ynecarboxylic esters. Intense fluorescence emission of selected compounds. The Journal of Organic Chemistry. 73: 5609-12. PMID 18558765 DOI: 10.1021/Jo800209Z |
0.485 |
|
| 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 |
0.645 |
|
| 2008 |
Ranu B, Dey R, Chattopadhyay K. Hiyama Cross-Coupling Using Palladium Nanoparticles Synfacts. 2008: 0776-0776. DOI: 10.1055/S-2008-1078432 |
0.384 |
|
| 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 |
0.673 |
|
| 2008 |
Bhadra S, Saha A, Ranu BC. One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: High diastereoselectivity achieved for vinyl dithiocarbamates Green Chemistry. 10: 1224-1230. DOI: 10.1039/B809200A |
0.529 |
|
| 2008 |
Adimurthy S, Ghosh S, Patoliya PU, Ramachandraiah G, Agrawal M, Gandhi MR, Upadhyay SC, Ghosh PK, Ranu BC. An alternative method for the regio- and stereoselective bromination of alkenes, alkynes, toluene derivatives and ketones using a bromide/bromate couple Green Chem.. 10: 232-237. DOI: 10.1039/B713829F |
0.572 |
|
| 2008 |
Ranu BC, Adak L, Banerjee S. Ionic liquid promoted interrupted Feist–Benary reaction with high diastereoselectivity Tetrahedron Letters. 49: 4613-4617. DOI: 10.1016/J.Tetlet.2008.05.083 |
0.611 |
|
| 2008 |
Ranu BC, Dey R, Chattopadhyay K. A one-pot efficient and fast Hiyama coupling using palladium nanoparticles in water under fluoride-free conditions Tetrahedron Letters. 49: 3430-3432. DOI: 10.1016/J.Tetlet.2008.03.121 |
0.492 |
|
| 2008 |
Ranu BC, Bhadra S, Adak L. Indium(III) chloride-catalyzed oxidative cleavage of carbon-carbon multiple bonds by tert-butyl hydroperoxide in water-a safer alternative to ozonolysis Tetrahedron Letters. 49: 2588-2591. DOI: 10.1016/J.Tetlet.2008.02.089 |
0.501 |
|
| 2008 |
Ranu BC, Saha A, Banerjee S. Catalysis by Ionic Liquids: Significant Rate Acceleration with the Use of [pmIm]Br in the Three-Component Synthesis of Dithiocarbamates European Journal of Organic Chemistry. 2008: 519-523. DOI: 10.1002/Ejoc.200700842 |
0.623 |
|
| 2008 |
Ranu BC, Banerjee S, Roy S. ChemInform Abstract: A Task Specific Basic Ionic Liquid, [bmIm]OH-Promoted Efficient, Green and One-Pot Synthesis of Tetrahydrobenzo[b]pyran Derivatives. Cheminform. 39. DOI: 10.1002/CHIN.200846133 |
0.35 |
|
| 2008 |
Ranu BC, Adak L, Banerjee S. ChemInform Abstract: Ionic Liquid Promoted Interrupted Feist-Benary Reaction with High Diastereoselectivity. Cheminform. 39. DOI: 10.1002/CHIN.200845117 |
0.388 |
|
| 2008 |
Ranu BC, Dey R, Chattopadhyay K. ChemInform Abstract: A One-Pot Efficient and Fast Hiyama Coupling Using Palladium Nanoparticles in Water under Fluoride-Free Conditions. Cheminform. 39. DOI: 10.1002/CHIN.200835083 |
0.34 |
|
| 2008 |
Ranu BC, Bhadra S, Adak L. ChemInform Abstract: Indium(III) Chloride Catalyzed Oxidative Cleavage of Carbon-Carbon Multiple Bonds by tert-Butyl Hydroperoxide in Water - A Safe Alternative to Ozonolysis. Cheminform. 39. DOI: 10.1002/CHIN.200831046 |
0.305 |
|
| 2008 |
Adimurthy S, Ghosh S, Patoliya PU, Ramachandraiah G, Agrawal M, Gandhi MR, Upadhyay SC, Ghosh PK, Ranu BC. ChemInform Abstract: An Alternative Method for the Regio- and Stereoselective Bromination of Alkenes, Alkynes, Toluene Derivatives and Ketones Using a Bromide/Bromate Couple. Cheminform. 39. DOI: 10.1002/CHIN.200825041 |
0.422 |
|
| 2008 |
Ranu BC, Saha A, Banerjee S. ChemInform Abstract: Catalysis by Ionic Liquids: Significant Rate Acceleration with the Use of [pmIm]Br in the Three-Component Synthesis of Dithiocarbamates. Cheminform. 39. DOI: 10.1002/CHIN.200821050 |
0.336 |
|
| 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 |
0.677 |
|
| 2008 |
Ranu BC, Banerjee S, Gupta J. ChemInform Abstract: Ionic Liquid-Promoted Stereoselective Synthesis of (Z)-Vinyl Bromides by [bmIm]OH under Organic Solvent-Free Conditions: A Green Approach. Cheminform. 39. DOI: 10.1002/CHIN.200806056 |
0.392 |
|
| 2008 |
Ranu BC, Banerjee S, Adak L. ChemInform Abstract: Regioselective Cross-Coupling of Allylindium Reagents with Activated Benzylic Bromides — A Simple and Efficient Procedure for the Synthesis of Terminal Alkenes. Cheminform. 39. DOI: 10.1002/CHIN.200803051 |
0.417 |
|
| 2007 |
Ranu BC, Chattopadhyay K, Adak L. Solvent-controlled highly selective bis- and monoallylation of active methylene compounds by allyl acetate with palladium(0) nanoparticle. Organic Letters. 9: 4595-8. PMID 17902686 DOI: 10.1021/Ol702099V |
0.493 |
|
| 2007 |
Ranu BC, Chattopadhyay K. A new route to the synthesis of (E)- and (Z)-2-alkene-4-ynoates and nitriles from vic-iiodo-(E)-alkenes catalyzed by Pd(0) nanoparticles in water. Organic Letters. 9: 2409-12. PMID 17488036 DOI: 10.1021/Ol0708121 |
0.47 |
|
| 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 |
0.738 |
|
| 2007 |
Ranu BC, Banerjee S. Homocoupling of Terminal Alkynes to 1,4-Disubstituted 1,3-Diynes Promoted by Copper(I) Iodide and a Task Specific Ionic Liquid, [bmim]OH — A Green Procedure. Cheminform. 38. DOI: 10.2174/157017806778559518 |
0.569 |
|
| 2007 |
Ranu BC, Adak L, Banerjee S. Efficient Regio- and Stereoselective Cleavage of Aziridines and Epoxides Using an Ionic Liquid as Reagent and Reaction Medium. Cheminform. 38. DOI: 10.1139/V07-040 |
0.64 |
|
| 2007 |
Ranu BC, Adak L, Banerjee S. Efficient regio- and stereo-selective cleavage of aziridines and epoxides using an ionic liquid as reagent and reaction medium Canadian Journal of Chemistry. 85: 366-371. DOI: 10.1139/V07-040 |
0.462 |
|
| 2007 |
Ranu BC, Banerjee S, Gupta J. Ionic Liquid–Promoted Stereoselective Synthesis of (Z)‐Vinyl Bromides by [bmIm]OH under Organic Solvent–Free Conditions: A Green Approach Synthetic Communications. 37: 2869-2876. DOI: 10.1080/00397910701471386 |
0.659 |
|
| 2007 |
Ranu BC, Mandal T. Efficient Synthesis of β‐Alkyl/Arylsulfanyl Carbonyl Compounds by In‐TMSCl‐Promoted Cleavage of Dialkyl/Diaryl Disulfides and Subsequent Michael Addition Synthetic Communications. 37: 1517-1523. DOI: 10.1080/00397910701229859 |
0.566 |
|
| 2007 |
Ranu BC, Adak L, Banerjee S. Halogenation of Carbonyl Compounds by an Ionic Liquid, [AcMIm]X, and Ceric Ammonium Nitrate (CAN) Australian Journal of Chemistry. 60: 358. DOI: 10.1071/Ch07061 |
0.601 |
|
| 2007 |
Ranu BC, Mandal T. A Simple, Efficient, and Green Procedure for the 1,4-Addition of Thiols to Conjugated Alkenes and Alkynes Catalyzed by Sodium Acetate in Aqueous Medium. Cheminform. 38. DOI: 10.1071/Ch06455 |
0.58 |
|
| 2007 |
Ranu BC, Mandal T. A Simple, Efficient, and Green Procedure for the 1,4-Addition of Thiols to Conjugated Alkenes and Alkynes Catalyzed by Sodium Acetate in Aqueous Medium Australian Journal of Chemistry. 60: 223. DOI: 10.1071/CH06455 |
0.51 |
|
| 2007 |
Ranu BC, Mandal T, Banerjee S, Dey SS. Ionic Liquid Promoted Regio- and Stereo-Selective Thiolysis of Epoxides—A Simple and Green Approach to β-Hydroxy- and β-Keto Sulfides Australian Journal of Chemistry. 60: 278. DOI: 10.1071/Ch06434 |
0.605 |
|
| 2007 |
Ranu BC, Ghosh S, Das A. Zinc Tetrafluoroborate Catalyzed Synthesis of Highly Substituted Pyrroles by a Solvent-Free Reaction. Cheminform. 38. DOI: 10.1070/Mc2006V016N04Abeh002287 |
0.558 |
|
| 2007 |
Ranu B, Mandal T. Water-Promoted Highly Selective Anti-Markovnikov Addition of Thiols to Unactivated Alkenes Synlett. 2007: 0925-0928. DOI: 10.1055/S-2007-973877 |
0.433 |
|
| 2007 |
Ranu BC, Banerjee S, Adak L. Regioselective cross-coupling of allylindium reagents with activated benzylic bromides—a simple and efficient procedure for the synthesis of terminal alkenes Tetrahedron Letters. 48: 7374-7379. DOI: 10.1016/J.Tetlet.2007.08.025 |
0.644 |
|
| 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 |
0.738 |
|
| 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 |
0.674 |
|
| 2007 |
Ranu BC, Banerjee S. Significant rate acceleration of the aza-Michael reaction in water Tetrahedron Letters. 48: 141-143. DOI: 10.1016/J.Tetlet.2006.10.142 |
0.573 |
|
| 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 |
0.766 |
|
| 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 |
0.73 |
|
| 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 |
0.644 |
|
| 2007 |
Ranu BC, Adak L, Banerjee S. Halogenation of Carbonyl Compounds by an Ionic Liquid, [AcMIm]X, and Ceric Ammonium Nitrate (CAN). Cheminform. 38. DOI: 10.1002/CHIN.200743035 |
0.269 |
|
| 2007 |
Ranu BC, Mandal T. Efficient Synthesis of β-Alkyl/Arylsulfanyl Carbonyl Compounds by In-TMSCl-Promoted Cleavage of Dialkyl/Diaryl Disulfides and Subsequent Michael Addition. Cheminform. 38. DOI: 10.1002/CHIN.200741070 |
0.411 |
|
| 2007 |
Ranu BC, Mandal T. Water-Promoted Highly Selective anti-Markovnikov Addition of Thiols to Unactivated Alkenes. Cheminform. 38. DOI: 10.1002/CHIN.200732084 |
0.283 |
|
| 2007 |
Adimurthy S, Ramachandraiah G, Bedekar AV, Ghosh S, Ranu BC, Ghosh PK. Eco-Friendly and Versatile Brominating Reagent Prepared from a Liquid Bromine Precursor. Cheminform. 38. DOI: 10.1002/CHIN.200708045 |
0.375 |
|
| 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 |
0.713 |
|
| 2006 |
Ranu BC, Chattopadhyay K, Banerjee S. Indium(I) iodide promoted cleavage of diphenyl diselenide and disulfide and subsequent palladium(0)-catalyzed condensation with vinylic bromides. A simple one-pot synthesis of vinylic selenides and sulfides. The Journal of Organic Chemistry. 71: 423-5. PMID 16388676 DOI: 10.1021/Jo052087I |
0.65 |
|
| 2006 |
Ranu B, Banerjee S. Homocoupling of Terminal Alkynes to 1,4-Disubstituted 1,3-Diynes Promoted by Copper(I) Iodide and a Task Specific Ionic Liquid, [bmim]OH -A Green Procedure Letters in Organic Chemistry. 3: 607-609. DOI: 10.2174/157017806778559518 |
0.311 |
|
| 2006 |
Ranu BC, Mandal T. Indium(I) iodide promoted cleavage of dialkyl disulfides Application of the Michael addition of thiolate anions to conjugated carbonyl compounds and regioselective ring opening of epoxides Canadian Journal of Chemistry. 84: 762-770. DOI: 10.1139/V06-065 |
0.467 |
|
| 2006 |
Ranu BC, Ghosh S, Das A. Zinc tetrafluoroborate-catalysed synthesis of highly substituted pyrroles by a solvent-free reaction Mendeleev Communications. 16: 220-221. DOI: 10.1070/MC2006V016N04ABEH002287 |
0.479 |
|
| 2006 |
Adimurthy S, Ramachandraiah G, Bedekar AV, Ghosh S, Ranu BC, Ghosh PK. Eco-friendly and versatile brominating reagent prepared from a liquid bromine precursor Green Chemistry. 8: 916. DOI: 10.1039/B606586D |
0.532 |
|
| 2006 |
Ranu BC, Mandal T. Indium(I) Iodide Promoted Cleavage of Dialkyl/Diaryl Disulfides and Subsequent anti-Markovnikov Addition to Styrenes: A New Route to Linear Thioethers. Cheminform. 37. DOI: 10.1016/J.Tetlet.2006.07.017 |
0.499 |
|
| 2006 |
Ranu BC, Mandal T. Indium(I) iodide promoted cleavage of dialkyl/diaryl disulfides and subsequent anti-Markovnikov addition to styrenes: a new route to linear thioethers Tetrahedron Letters. 47: 6911-6914. DOI: 10.1016/J.TETLET.2006.07.017 |
0.296 |
|
| 2006 |
Ranu BC, Mandal T. An indium–TMSCl promoted reaction of diphenyl diselenides and aldehydes: novel routes to selenoacetals and alkyl phenyl selenides Tetrahedron Letters. 47: 5677-5680. DOI: 10.1016/J.Tetlet.2006.06.012 |
0.55 |
|
| 2006 |
Ranu BC, Mandal T. Indium(I) iodide as a radical initiator: intramolecular cyclization of functionalized bromo-alkynes to substituted tetrahydrofurans Tetrahedron Letters. 47: 2859-2861. DOI: 10.1016/J.TETLET.2006.02.135 |
0.383 |
|
| 2006 |
Ranu BC, Banerjee S, Das A. Catalysis by Ionic Liquids: Cyclopropyl Carbinyl Rearrangements Catalyzed by [pmim]Br under Organic Solvent Free Conditions. Cheminform. 37. DOI: 10.1016/J.Tetlet.2005.12.003 |
0.607 |
|
| 2006 |
Ranu BC, Banerjee S, Das A. Catalysis by ionic liquids: cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions Tetrahedron Letters. 47: 881-884. DOI: 10.1016/J.TETLET.2005.12.003 |
0.342 |
|
| 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 |
0.741 |
|
| 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 |
0.686 |
|
| 2006 |
Ranu BC, Banerjee S. Indium Triflate Catalyzed Rearrangement of Aryl-Substituted Cyclopropyl Carbinols to 1,4-Disubstituted 1,3-Butadienes European Journal of Organic Chemistry. 2006: 3012-3015. DOI: 10.1002/Ejoc.200600037 |
0.647 |
|
| 2006 |
Ranu BC, Mandal T. An Indium—TMSCl Promoted Reaction of Diphenyl Diselenides and Aldehydes: Novel Routes to Selenoacetals and Alkyl Phenyl Selenides. Cheminform. 37. DOI: 10.1002/CHIN.200647193 |
0.446 |
|
| 2006 |
Ranu BC, Banerjee S. Indium Triflate Catalyzed Rearrangement of Aryl-Substituted Cyclopropyl Carbinols to 1,4-Disubstituted 1,3-Butadienes. Cheminform. 37. DOI: 10.1002/CHIN.200645084 |
0.481 |
|
| 2006 |
Ranu BC. Use of Ionic Liquids as Green Catalysts and Reagents as well as Reaction Media in Chemical Transformations Cheminform. 37. DOI: 10.1002/chin.200638256 |
0.376 |
|
| 2006 |
Ranu BC, Mandal T. Indium(I) Iodide as a Radical Initiator: Intramolecular Cyclization of Functionalized Bromo-Alkynes to Substituted Tetrahydrofurans. Cheminform. 37. DOI: 10.1002/CHIN.200632117 |
0.383 |
|
| 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 |
0.731 |
|
| 2005 |
Ranu BC, Banerjee S. Ionic liquid as catalyst and reaction medium. The dramatic influence of a task-specific ionic liquid, [bmIm]OH, in Michael addition of active methylene compounds to conjugated ketones, carboxylic esters, and nitriles. Organic Letters. 7: 3049-52. PMID 15987202 DOI: 10.1021/Ol051004H |
0.605 |
|
| 2005 |
Ranu BC, Banerjee S. Ionic liquid as reagent. A green procedure for the regioselective conversion of epoxides to vicinal-halohydrins using [AcMIm]X under catalyst- and solvent-free conditions. The Journal of Organic Chemistry. 70: 4517-9. PMID 15903336 DOI: 10.1021/Jo0500885 |
0.594 |
|
| 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 |
0.673 |
|
| 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 |
0.649 |
|
| 2005 |
Ranu BC, Das A. A Simple, General and Improved Procedure for Phosphorylation of Alcohols Catalyzed by Indium(III) Chloride. Cheminform. 36. DOI: 10.1002/CHIN.200513187 |
0.302 |
|
| 2005 |
Ranu BC, Banerjee S, Das A. Selective Reductive Cleavage of 2,3-Epoxybromides by the InCl3?NaBH4 Reagent System. Cheminform. 36. DOI: 10.1002/CHIN.200508035 |
0.324 |
|
| 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 |
0.734 |
|
| 2005 |
Ranu B, Das A. A Convenient Synthesis of ?-Phenylselenocarbonyl Compounds by In-TMSCl Promoted Cleavage of Diphenyl Diselenide and Subsequent Michael Addition Advanced Synthesis & Catalysis. 347: 712-714. DOI: 10.1002/Adsc.200404355 |
0.514 |
|
| 2004 |
Ranu BC, Mandal T. Indium(I) iodide-promoted cleavage of diaryl diselenides and disulfides and subsequent condensation with alkyl or acyl halides. One-pot efficient synthesis of diorganyl selenides, sulfides, selenoesters, and thioesters. The Journal of Organic Chemistry. 69: 5793-5. PMID 15307762 DOI: 10.1021/Jo0493727 |
0.566 |
|
| 2004 |
Ranu BC, Dey SS, Samanta S. Indium(III) chloride – catalyzed Michael addition of thiols to chalcones : A remarkable solvent effect Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.306 |
0.73 |
|
| 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 |
0.704 |
|
| 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 |
0.664 |
|
| 2004 |
Ranu BC, Das A. Molten Salt as a Green Reaction Medium: Efficient and Chemoselective Dithioacetalization and Oxathioacetalization of Aldehydes Mediated by Molten Tetrabutylammonium Bromide. Cheminform. 35. DOI: 10.1071/Ch03318 |
0.53 |
|
| 2004 |
Ranu BC, Das A. Molten Salt as a Green Reaction Medium: Efficient and Chemoselective Dithioacetalization and Oxathioacetalization of Aldehydes Mediated by Molten Tetrabutylammonium Bromide Australian Journal of Chemistry. 57: 605. DOI: 10.1071/CH03318 |
0.453 |
|
| 2004 |
Ranu BC, Mandal T. Indium(I) Iodide Promoted Cleavage of Dialkyl Disulfides and Subsequent Michael Addition of Thiolate Anions to Conjugated Carbonyl Compounds. Cheminform. 35. DOI: 10.1055/S-2004-825583 |
0.506 |
|
| 2004 |
Ranu BC, Banerjee S, Das A. Selective reductive cleavage of 2,3-epoxybromides by the InCl3–NaBH4 reagent system Tetrahedron Letters. 45: 8579-8581. DOI: 10.1016/J.Tetlet.2004.09.120 |
0.573 |
|
| 2004 |
Ranu BC, Das A. Indium(I) Iodide Promoted Highly Selective 1,2-Addition of Allyl and Benzyl Groups to α,β-Unsaturated Nitriles under Sonication: A New Synthesis of Conjugated Imines. Cheminform. 35. DOI: 10.1016/J.Tetlet.2004.07.098 |
0.5 |
|
| 2004 |
Ranu BC, Das A. Indium(I) iodide promoted highly selective 1,2-addition of allyl and benzyl groups to α,β-unsaturated nitriles under sonication: a new synthesis of conjugated imines Tetrahedron Letters. 45: 6875-6877. DOI: 10.1016/J.TETLET.2004.07.098 |
0.398 |
|
| 2004 |
Ranu BC, Dey SS. Catalysis by Ionic Liquid: A Simple, Green and Efficient Procedure for the Michael Addition of Thiols and Thiophosphate to Conjugated Alkenes in Ionic Liquid, [pmIm]Br. Cheminform. 35. DOI: 10.1016/J.Tet.2004.03.052 |
0.536 |
|
| 2004 |
Ranu BC, Dey SS. Catalysis by ionic liquid: a simple, green and efficient procedure for the Michael addition of thiols and thiophosphate to conjugated alkenes in ionic liquid, [pmIm]Br Tetrahedron. 60: 4183-4188. DOI: 10.1016/J.TET.2004.03.052 |
0.345 |
|
| 2004 |
Ranu BC, Samanta S. Reduction of Activated Conjugated Alkenes by the InCl3—NaBH4 Reagent System. Cheminform. 35. DOI: 10.1002/CHIN.200404038 |
0.646 |
|
| 2004 |
Ranu BC, Samanta S. Remarkably Selective Reduction of the α,β-Carbon—Carbon Double Bond in Highly Activated α,β,γ,δ-Unsaturated Alkenes by the InCl3—NaBH4 Reagent System. Cheminform. 35. DOI: 10.1002/CHIN.200404037 |
0.638 |
|
| 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 |
0.806 |
|
| 2003 |
Ranu BC, Samanta S. Remarkably selective reduction of the alpha,beta-carbon-carbon double bond in highly activated alpha,beta,gamma,delta-unsaturated alkenes by the InCl3-NaBH4 reagent system. The Journal of Organic Chemistry. 68: 7130-2. PMID 12946166 DOI: 10.1021/Jo0347821 |
0.607 |
|
| 2003 |
Ranu BC, Mandal T, Samanta S. Indium(I) iodide-mediated cleavage of diphenyl diselenide. An efficient one-pot procedure for the synthesis of unsymmetrical diorganyl selenides. Organic Letters. 5: 1439-41. PMID 12713293 DOI: 10.1021/Ol034178C |
0.734 |
|
| 2003 |
Ranu BC, Dey SS, Bag S. A simple and green procedure for the synthesis of N,N'-disubstituted thioureas on the surface of alumina under microwave irradiation Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.903 |
0.436 |
|
| 2003 |
Ranu BC, Dutta J, Das A. Zinc Tetrafluoroborate-Catalyzed Efficient Conversion of Aldehydes to Geminal Diacetates and Cyanoacetates Chemistry Letters. 32: 366-367. DOI: 10.1246/Cl.2003.366 |
0.555 |
|
| 2003 |
Ranu BC, Dutta P. A Simple and Convenient Procedure for the Conversion of Esters to Secondary Amides. Cheminform. 34. DOI: 10.1081/Scc-120015715 |
0.465 |
|
| 2003 |
Ranu BC, Dutta P. A Simple and Convenient Procedure for the Conversion of Esters to Secondary Amides Synthetic Communications. 33: 297-301. DOI: 10.1081/SCC-120015715 |
0.36 |
|
| 2003 |
Ranu BC, Das A, Hajra A. Dichloroindium Hydride(Cl2InH): A Convenient Reagent for Stereoselective Reductionofvic-Dibromides to (E)-Alkenes Synthesis. 2003: 1012-1014. DOI: 10.1055/S-2003-39165 |
0.549 |
|
| 2003 |
Ranu BC, Dey SS, Hajra A. Highly efficient acylation of alcohols, amines and thiols under solvent-free and catalyst-free conditions Green Chemistry. 5: 44-46. DOI: 10.1039/B211238H |
0.633 |
|
| 2003 |
Ranu BC, Das A, Samanta S. Catalysis by Ionic Liquids: Solvent-Free Efficient Transthioacetalization of Acetals by Molten Tetrabutylammonium Bromide. Cheminform. 34. DOI: 10.1039/B204363G |
0.68 |
|
| 2003 |
Ranu BC, Samanta S. Remarkably selective reduction of the α,β-carbon-carbon double bond in highly activated α,β,γ,δ-unsaturated alkenes by the InCl3-NaBH4 reagent system Journal of Organic Chemistry. 68: 7130-7132. DOI: 10.1021/jo0347821 |
0.649 |
|
| 2003 |
Ranu BC, Dey SS. An efficient synthesis of pyrroles by a one-pot, three-component condensation of a carbonyl compound, an amine and a nitroalkene in a molten ammonium salt Tetrahedron Letters. 44: 2865-2868. DOI: 10.1016/S0040-4039(03)00439-8 |
0.551 |
|
| 2003 |
Ranu BC, Dey SS, Hajra A. Catalysis by an Ionic Liquid: Efficient Conjugate Addition of Thiols to Electron Deficient Alkenes Catalyzed by Molten Tetrabutylammonium Bromide under Solvent-Free Conditions. Cheminform. 34. DOI: 10.1016/S0040-4020(03)00289-8 |
0.671 |
|
| 2003 |
Ranu BC, Dey SS, Hajra A. Catalysis by an ionic liquid: efficient conjugate addition of thiols to electron deficient alkenes catalyzed by molten tetrabutylammonium bromide under solvent-free conditions Tetrahedron. 59: 2417-2421. DOI: 10.1016/S0040-4020(03)00289-8 |
0.587 |
|
| 2003 |
Ranu BC, Hajra A, Dey SS, Jana U. Efficient microwave-assisted synthesis of quinolines and dihydroquinolines under solvent-free conditions Tetrahedron. 59: 813-819. DOI: 10.1016/S0040-4020(02)01587-9 |
0.69 |
|
| 2003 |
Ranu BC, Samanta S. Reduction of activated conjugated alkenes by the InCl3-NaBH 4 reagent system Tetrahedron. 59: 7901-7906. DOI: 10.1016/J.Tet.2003.08.022 |
0.682 |
|
| 2003 |
Ranu BC, Das A, Hajra A. Dichloroindium Hydride (Cl2InH): A Convenient Reagent for Stereoselective Reduction of vic-Dibromides to (E)-Alkenes. Cheminform. 34. DOI: 10.1002/CHIN.200341060 |
0.564 |
|
| 2003 |
Ranu BC, Dutta J, Das A. Zinc Tetrafluoroborate Catalyzed Efficient Conversion of Aldehydes to Geminal Diacetates and Cyanoacetates. Cheminform. 34. DOI: 10.1002/CHIN.200334049 |
0.424 |
|
| 2003 |
Ranu BC, Dey SS. An Efficient Synthesis of Pyrroles by a One-Pot, Three-Component Condensation of a Carbonyl Compounds, an Amine and a Nitroalkene in a Molten Ammonium Salt. Cheminform. 34. DOI: 10.1002/CHIN.200327094 |
0.4 |
|
| 2003 |
Ranu BC, Hajra A, Dey SS, Jana U. Efficient Microwave-Assisted Synthesis of Quinolines and Dihydroquinolines under Solvent-Free Conditions. Cheminform. 34. DOI: 10.1002/CHIN.200322141 |
0.597 |
|
| 2003 |
Rigby HL, Neveu M, Pauley D, Ranu BC, Hudlicky T. 3‐Hydroxy‐1‐cyclohexene‐1‐carboxaldehyde Organic Syntheses. 205-205. DOI: 10.1002/0471264180.Os067.28 |
0.651 |
|
| 2003 |
Ranu BC, Dey SS, Bag S. A simple and green procedure for the synthesis of symmetrical N,N'-disubstituted thioureas on the surface of alumina under microwave irradiation Arkivoc. 2003: 14-20. |
0.367 |
|
| 2002 |
Ranu BC, Samanta S, Hajra A. Indium-mediated allylation of beta-keto phosphonates. The Journal of Organic Chemistry. 66: 7519-21. PMID 11681972 DOI: 10.1021/Jo0105134 |
0.695 |
|
| 2002 |
Ranu BC, Dey SS, Hajra A. Solvent-free, catalyst-free Michael-type addition of amines to electron-deficient alkenes Arkivoc. 2002. DOI: 10.3998/Ark.5550190.0003.709 |
0.658 |
|
| 2002 |
Ranu BC, Samanta S, Hajra A. Unusual Cleavage of Ethers by Thiophenol on the Surface of Silica Gel Impregnated with Indium(III) Chloride under Microwave Irradiation: Efficient Procedure for the Synthesis of Thioethers through Transthioetherification Synlett. 2002: 0987-0989. DOI: 10.1055/S-2002-31911 |
0.754 |
|
| 2002 |
Ranu BC, Das A, Samanta S. Highly Efficient Transthioacetalization of O,O-Acetals Catalyzed by Indium(III) Chloride Synlett. 2002: 0727-0730. DOI: 10.1055/S-2002-25347 |
0.644 |
|
| 2002 |
Ranu BC, Hajra A. A simple and green procedure for the synthesis of α-aminophosphonate by a one-pot three-component condensation of carbonyl compound, amine and diethyl phosphite without solvent and catalyst Green Chem.. 4: 551-554. DOI: 10.1039/B205747F |
0.674 |
|
| 2002 |
Ranu BC, Hajra A, Dey SS. A Practical and Green Approach towards Synthesis of Dihydropyrimidinones without Any Solvent or Catalyst Organic Process Research & Development. 6: 817-818. DOI: 10.1021/Op0255478 |
0.52 |
|
| 2002 |
Ranu BC, Samanta S. Use of indium hydride (Cl2InH) for chemoselective reduction of the carbon-carbon double bond in conjugated alkenes Tetrahedron Letters. 43: 7405-7407. DOI: 10.1016/S0040-4039(02)01668-4 |
0.681 |
|
| 2002 |
Ranu BC, Samanta S, Das A. Reduction of trihalomethyl carbinols and their acetates, mesylates and tosylates by indium metal Tetrahedron Letters. 43: 5993-5995. DOI: 10.1016/S0040-4039(02)01262-5 |
0.674 |
|
| 2002 |
Ranu BC, Dey SS, Hajra A. Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide Tetrahedron. 58: 2529-2532. DOI: 10.1016/S0040-4020(02)00132-1 |
0.677 |
|
| 2002 |
Ranu BC, Samanta S, Guchhait SK. Zinc tetrafluoroborate catalyzed Mannich-type reaction of aldimines and silyl enol ethers in aqueous medium Tetrahedron. 58: 983-988. DOI: 10.1016/S0040-4020(01)01177-2 |
0.825 |
|
| 2001 |
Ranu BC, Dutta J, Guchhait SK. Selective reduction of terminal alkynes to alkenes by indium metal. The Journal of Organic Chemistry. 66: 5624-6. PMID 11485495 DOI: 10.1021/Jo010262Z |
0.776 |
|
| 2001 |
Ranu BC, Dutta J, Guchhait SK. Indium metal as a reducing agent. Selective reduction of the carbon-carbon double bond in highly activated conjugated alkenes. Organic Letters. 3: 2603-5. PMID 11483071 DOI: 10.1021/Ol016296A |
0.786 |
|
| 2001 |
Ranu BC, Samanta S, Guchhait SK. Stereoselective reduction of aryl-substituted gem-dibromides to vinyl bromides by indium metal Journal of Organic Chemistry. 66: 4102-4103. PMID 11375049 DOI: 10.1021/Jo0102314 |
0.807 |
|
| 2001 |
Ranu BC, Hajra A. Highly selective one-pot conversion of THP and MOM ethers to acetates by indium triiodide-catalysed deprotection and subsequent transesterification by ethyl acetate Journal of the Chemical Society-Perkin Transactions 1. 2262-2265. DOI: 10.1039/B104055N |
0.652 |
|
| 2001 |
Ranu BC, Hajra A. Indium triiodide catalysed one-step conversion of tetrahydropyranyl ethers to acetates with high selectivity Journal of the Chemical Society-Perkin Transactions 1. 355-357. DOI: 10.1039/B100014B |
0.64 |
|
| 2001 |
Ranu BC, Hajra A. Synthesis of alkyl-substituted pyrroles by three-component coupling of carbonyl compound, amine and nitro-alkane/alkene on a solid surface of silica gel/alumina under microwave irradiation Tetrahedron. 57: 4767-4773. DOI: 10.1016/S0040-4020(01)00400-8 |
0.677 |
|
| 2001 |
Ranu BC, Hajra A, Jana U. ChemInform Abstract: Indium(III) Chloride-Catalyzed One-Pot Synthesis of Dihydropyrimidinones by a Three-Component Coupling of 1,3-Dicarbonyl Compounds, Aldehydes, and Urea: An Improved Procedure for the Biginelli Reaction. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200105123 |
0.64 |
|
| 2001 |
Ranu BC, Dutta P, Sarkar A. ChemInform Abstract: An Efficient and General Method for Ester Hydrolysis on the Surface of Silica Gel Catalyzed by Indium Triiodide under Microwave Irradiation. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200104079 |
0.371 |
|
| 2001 |
Ranu BC. ChemInform Abstract: Indium Metal and Its Halides in Organic Synthesis Cheminform. 32: no-no. DOI: 10.1002/CHIN.200102256 |
0.34 |
|
| 2000 |
Ranu BC, Hajra A, Jana U. Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: an improved procedure for the Biginelli reaction. The Journal of Organic Chemistry. 65: 6270-2. PMID 10987976 DOI: 10.1021/Jo000711F |
0.527 |
|
| 2000 |
Ranu BC, Dutta P, Sarkar A. An Efficient and General Method for Ester Hydrolysis on the Surface of Silica Gel Catalyzed by Indium Triiodide Under Microwave Irradiation Synthetic Communications. 30: 4167-4171. DOI: 10.1080/00397910008087033 |
0.472 |
|
| 2000 |
Ranu BC, Hajra A, Jana U. Microwave-Assisted Synthesis of Substituted Pyrroles by a Three-Component Coupling of α,β-Unsaturated Carbonyl Compounds, Amines and Nitroalkanes on the Surface of Silica Gel Synlett. 2000: 75-76. DOI: 10.1055/S-2000-6449 |
0.678 |
|
| 2000 |
Ranu BC, Dutta P, Sarkar A. Highly selective acylation of alcohols and amines by an indium triiodide-catalysed transesterification process Journal of the Chemical Society-Perkin Transactions 1. 2223-2225. DOI: 10.1039/B002181O |
0.412 |
|
| 2000 |
Ranu BC, Guchhait SK, Ghosh K, Patra A. Construction of bicyclo[2.2.2]octanone systems by microwave-assisted solid phase Michael addition followed by Al2O3-mediated intramolecular aldolisation. An eco-friendly approach Green Chemistry. 2: 5-6. DOI: 10.1039/A907689A |
0.784 |
|
| 2000 |
Ranu BC, Hajra A, Jana U. Microwave-assisted simple synthesis of quinolines from anilines and alkyl vinyl ketones on the surface of silica gel in the presence of indium(III) chloride Tetrahedron Letters. 41: 531-533. DOI: 10.1016/S0040-4039(99)02111-5 |
0.685 |
|
| 2000 |
Ranu BC, Dutta P, Sarkar A. ChemInform Abstract: Highly Selective Acylation of Alcohols and Amines by an Indium Triiodide-Catalyzed Transesterification Process. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200047076 |
0.334 |
|
| 2000 |
Ranu BC, Guchhait SK, Saha M. ChemInform Abstract: A Convenient and Efficient Procedure for Selective Deprotection of Acetates by Titanium(IV) Isopropoxide. Cheminform. 31: no-no. DOI: 10.1002/chin.200040058 |
0.36 |
|
| 2000 |
Ranu B. Indium Metal and Its Halides in Organic Synthesis European Journal of Organic Chemistry. 2000: 2347-2356. DOI: 10.1002/1099-0690(200007)2000:13<2347::Aid-Ejoc2347>3.0.Co;2-X |
0.565 |
|
| 1999 |
Ranu BC, Dutta P, Sarkar A. Indium as a reducing agent. Chemoselective reduction of α-halocarbonyl compounds and benzyl halides by indium metal in water under sonication Journal of the Chemical Society-Perkin Transactions 1. 1139-1140. DOI: 10.1039/A901493D |
0.468 |
|
| 1999 |
Ranu BC, Jana U, Majee A. Selective monoacylation of ferrocene Green Chemistry. 1: 33-34. DOI: 10.1039/A808890J |
0.649 |
|
| 1999 |
Ranu BC, Hajra A, Jana U. General Procedure for the Synthesis of α-Amino Phosphonates from Aldehydes and Ketones Using Indium(III) Chloride as a Catalyst Organic Letters. 1: 1141-1143. DOI: 10.1021/Ol990079G |
0.69 |
|
| 1999 |
Ranu BC, Jana U. A New Redundant Rearrangement of Aromatic Ring Fused Cyclic α-Hydroxydithiane Derivatives. Synthesis of Aromatic Ring Fused Cyclic 1,2-Diketones with One-Carbon Ring Expansion The Journal of Organic Chemistry. 64: 6380-6386. DOI: 10.1021/Jo990634S |
0.483 |
|
| 1999 |
Ranu BC, Jana U, Majee A. A simple and efficient method for selective deprotection of t-butyldimethylsilyl ethers by zinc tetrafluoroborate in water Tetrahedron Letters. 40: 1985-1988. DOI: 10.1016/S0040-4039(99)00097-0 |
0.617 |
|
| 1998 |
Ranu BC, Dutta P, Sarkar A. A Simple and Efficient Procedure for Transesterification Catalyzed by Indium Triiodide. The Journal of Organic Chemistry. 63: 6027-6028. PMID 11672209 DOI: 10.1021/Jo980157Y |
0.452 |
|
| 1998 |
Ranu BC, Jana U, Sarkar A. Regioselective Reduction of Quinolines and Related Systems to 1,2,3,4-Tetrahydro Derivatives with Zinc Borohydride Synthetic Communications. 28: 485-492. DOI: 10.1080/00397919808005103 |
0.301 |
|
| 1998 |
Ranu BC, Guchhait SK, Sarkar A. Stereoselective debromination of aryl-substituted vic-dibromide with indium metal Chemical Communications. 2113-2114. DOI: 10.1039/A806530F |
0.793 |
|
| 1998 |
Ranu BC, Jana U. Indium(III) Chloride-Promoted Rearrangement of Epoxides: A Selective Synthesis of Substituted Benzylic Aldehydes and Ketones The Journal of Organic Chemistry. 63: 8212-8216. DOI: 10.1021/Jo980793W |
0.579 |
|
| 1998 |
Ranu BC, Guchhait SK, Ghosh K. Chemoselective Hydrogenation of α,β-Unsaturated Sulfones and Phosphonates via Palladium-Assisted Hydrogen Transfer by Ammonium Formate The Journal of Organic Chemistry. 63: 5250-5251. DOI: 10.1021/Jo980128N |
0.779 |
|
| 1998 |
Ranu BC, Majee A, Sarkar A. One-Pot Reductive Amination of Conjugated Aldehydes and Ketones with Silica Gel and Zinc Borohydride The Journal of Organic Chemistry. 63: 370-373. DOI: 10.1021/Jo971117H |
0.54 |
|
| 1998 |
Ranu BC, Dutta P, Sarkar A. Indium promoted reductive homocoupling of alkyl and aryl halides Tetrahedron Letters. 39: 9557-9558. DOI: 10.1016/S0040-4039(98)02123-6 |
0.538 |
|
| 1998 |
Avalos M, Babiano R, Bravo J, Cintas P, Jiménez J, Palacios JC, Ranu BC. Cycloadditions with clays and alumina without solvents Tetrahedron Letters. 39: 2013-2016. DOI: 10.1016/S0040-4039(98)00159-2 |
0.506 |
|
| 1997 |
Ranu BC, Saha M, Bhar S. Surface-Mediated Solid Phase Reaction. IX. A Convenient Procedure for Aldol Reaction of Ketene Silyl Acetals with Aldehydes on the Solid Surface of Alumina Synthetic Communications. 27: 3065-3077. DOI: 10.1080/00397919708005012 |
0.519 |
|
| 1997 |
Ranu BC, Saha M, Bhar S. Microwave Assisted Michael Addition of Cycloalkenones and Substituted Enones on the Surface of Alumina in Dry Media Synthetic Communications. 27: 621-626. DOI: 10.1080/00397919708003334 |
0.465 |
|
| 1997 |
Ranu BC, Majee A. Indium-Mediated Regioselective Markovnikov Allylation Of Unactivated Terminal Alkynes Chemical Communications. 1225-1226. DOI: 10.1039/A702241G |
0.665 |
|
| 1997 |
Ranu BC, Sarkar aA, Majee A. Reduction of Imines with Zinc Borohydride Supported on Silica Gel. Highly Stereoselective Synthesis of Substituted Cyclohexylamines Journal of Organic Chemistry. 62: 1841-1842. DOI: 10.1021/Jo961736A |
0.698 |
|
| 1996 |
Ranu BC, Sarkar A, Saha M, Bhar S. Use of 1-menthyl ester as chiral auxiliary in the synthesis of useful chiral synthons Pure and Applied Chemistry. 68: 775-777. DOI: 10.1351/Pac199668030775 |
0.519 |
|
| 1996 |
Ranu BC, Bhar S. DEALKYLATION OF ETHERS. A REVIEW Organic Preparations and Procedures International. 28: 371-409. DOI: 10.1080/00304949609356549 |
0.323 |
|
| 1996 |
Ranu BC, Bhar S, Patra A, Nayak NP, Mukherjee M. Rearrangement of dithianylcyclobutachromanol derivatives to 1,2,2a,8,9,9a-hexahydrocyclobuta[b][1]benzoxepin-8,9-dione Chemical Communications. 1965-1966. DOI: 10.1039/Cc9960001965 |
0.331 |
|
| 1996 |
Ranu BC, Ghosh K, Jana U. Simple and Improved Procedure for Regioselective Acylation of Aromatic Ethers with Carboxylic Acids on the Solid Surface of Alumina in the Presence of Trifluoroacetic Anhydride The Journal of Organic Chemistry. 61: 9546-9547. DOI: 10.1021/Jo9615413 |
0.462 |
|
| 1996 |
Ranu BC, Majee A, Das AR. A convenient synthesis of β,γ-unsaturated ketones through zinc-mediated allylation of acid chlorides Tetrahedron Letters. 37: 1109-1112. DOI: 10.1016/0040-4039(95)02317-8 |
0.799 |
|
| 1995 |
Ranu BC, Majee A, Das AR. Surface-Mediated Solid Phase Reaction. PART 7.1A Simple and Convenient Procedure for the Methoxymethylation of Alcohols with Methoxymethyl Chloride on the Surface of Alumina Synthetic Communications. 25: 363-367. DOI: 10.1080/00397919508011367 |
0.648 |
|
| 1995 |
Bhar S, Ranu BC. Zinc-Promoted Selective Cleavage of Ethers in Presence of Acyl Chloride The Journal of Organic Chemistry. 60: 745-747. DOI: 10.1021/Jo00108A048 |
0.452 |
|
| 1995 |
Ranu BC, Majee A, Das AR. Facile and efficient synthesis of homoallylic alcohols using allyl bromide and commercial zinc dust Tetrahedron Letters. 36: 4885-4888. DOI: 10.1016/0040-4039(95)00877-F |
0.778 |
|
| 1995 |
RANU BC, SARKAR A. ChemInform Abstract: Regio- and Stereoselective Hydrogenation of Conjugated Carbonyl Compounds via Palladium Assisted Hydrogen Transfer by Ammonium Formate. Cheminform. 26: no-no. DOI: 10.1002/chin.199516064 |
0.322 |
|
| 1994 |
Ranu BC, Saha M, Bhar S. Surface-mediated solid phase reaction. Part 6. Mukaiyama–Michael addition of silyl enol ethers to alkyl vinyl ketones on the surface of alumina: a simple and convenient method for the synthesis of 1,5-diketones Journal of the Chemical Society-Perkin Transactions 1. 2197-2199. DOI: 10.1039/P19940002197 |
0.536 |
|
| 1994 |
Ranu BC, Das AR. Two-carbon ring expansion through free cyclobutylcarbinyl radical fragmentation Journal of the Chemical Society-Perkin Transactions 1. 921-922. DOI: 10.1039/P19940000921 |
0.658 |
|
| 1994 |
Ranu BC, Saha M. A Simple, Efficient, and Selective Method for Tetrahydropyranylation of Alcohols on a Solid Phase of Alumina Impregnated with Zinc Chloride The Journal of Organic Chemistry. 59: 8269-8270. DOI: 10.1021/Jo00105A054 |
0.409 |
|
| 1994 |
Ranu BC, Sarkar A, Chakraborty R. Reduction of Azides with Zinc Borohydride The Journal of Organic Chemistry. 59: 4114-4116. DOI: 10.1021/Jo00094A021 |
0.52 |
|
| 1994 |
Ranu BC, Sarkar A. Regio- and stereoselective hydrogenation of conjugated carbonyl compounds via palladium assisted hydrogen transfer by ammonium formate Tetrahedron Letters. 35: 8649-8650. DOI: 10.1016/S0040-4039(00)78461-9 |
0.427 |
|
| 1994 |
Ranu BC, Sarkar A, Saha M, Chakraborty R. Silica gel supported zinc borohydride. A novel reagent for hydration of unactivated alkenes and alkynes Tetrahedron. 50: 6579-6584. DOI: 10.1016/S0040-4020(01)89688-5 |
0.532 |
|
| 1993 |
Ranu BC. Zinc Borohydride - A Reducing Agent with High Potential Synlett. 1993: 885-892. DOI: 10.1055/S-1993-22640 |
0.526 |
|
| 1993 |
Ranu BC, Saha M, Bhar S. Surface-mediated solid phase reaction. Mukaiyama-Michael addition of silyl enol ethers to methyl vinyl ketone on the surface of alumina Tetrahedron Letters. 34: 1989-1990. DOI: 10.1016/S0040-4039(00)91983-X |
0.499 |
|
| 1993 |
Ranu BC, Chakraborty R, Saha M. An unusual regioselective anti-markovnikov hydration of alkenes with zinc borohydride on silica gel support Tetrahedron Letters. 34: 4659-4662. DOI: 10.1016/S0040-4039(00)60650-0 |
0.508 |
|
| 1993 |
Ranu BC, Chakraborty R. Surface-mediated solid phase reaction. Aldol reaction of silyl enol ethers with aldehydes on a solid surface of neutral alumina: selectivity for anti aldols Tetrahedron. 49: 5333-5338. DOI: 10.1016/S0040-4020(01)82382-6 |
0.488 |
|
| 1992 |
Chakraborty R, Das AR, Ranu BC. Ion Exchange Resin-Mediated Hydrolytic Cleavage of α-Nitroepoxides. Simple One-Pot Synthesis of α-Hydroxyketones Synthetic Communications. 22: 1523-1528. DOI: 10.1080/00397919208021623 |
0.681 |
|
| 1992 |
Ranu BC, Das AR. Silica gel-supported zinc borohydride. Part 3. Regioselective reductive cleavage of methylenecycloalkane oxides to the less-substituted alcohols Journal of the Chemical Society-Perkin Transactions 1. 1881-1882. DOI: 10.1039/P19920001881 |
0.68 |
|
| 1992 |
Ranu BC, Das AR. Selective reduction of carboxylic acids with zinc borohydride in the presence of trifluoroacetic anhydride Journal of the Chemical Society-Perkin Transactions 1. 1561-1562. DOI: 10.1039/P19920001561 |
0.688 |
|
| 1992 |
Ranu BC, Bhar S. Surface-mediated solid-phase reaction. Part 2. Highly selective mono- and di-C-alkylation of 1,3-dicarbonyl compounds on the surface of alumina Journal of the Chemical Society-Perkin Transactions 1. 365-368. DOI: 10.1039/P19920000365 |
0.493 |
|
| 1992 |
Ranu BC, Bhar S, Chakraborti R. Synthesis of .beta.-keto 1,3-dithianes from acetylenic ketones The Journal of Organic Chemistry. 57: 7349-7352. DOI: 10.1021/Jo00052A064 |
0.404 |
|
| 1992 |
Ranu BC, Das AR. Highly selective reduction of 2-nitrocycloalkanones to 2-nitrocycloalkanols with zinc borohydride in DME Tetrahedron Letters. 33: 2361-2362. DOI: 10.1016/S0040-4039(00)74211-0 |
0.692 |
|
| 1992 |
Ranu BC, Bhar S. Surface-mediated solid phase reaction: Dramatic improvement of Michael reaction on the surface of alumina Tetrahedron. 48: 1327-1332. DOI: 10.1016/S0040-4020(01)90794-X |
0.494 |
|
| 1992 |
Chakraborty R, Basu MK, Ranu BC. α-Hydroxycyclobutane rearrangement followed by retroaldol cleavage: A novel and powerful technology for the stereocontrolled construction of carbocyclic systems. An easy access to angularly functionalised trans-fused cycloheptanoids Tetrahedron. 48: 8849-8854. DOI: 10.1016/S0040-4020(01)89456-4 |
0.458 |
|
| 1992 |
Ranu BC, Chakraborty R. Reduction of conjugated nitroalkenes with zinc borohydride. A mild method for converting monosubstituted nitroalkenes to nitroalkanes and disubstituted ones to oximes Tetrahedron. 48: 5317-5322. DOI: 10.1016/S0040-4020(01)89028-1 |
0.518 |
|
| 1991 |
Ranu BC, Chakraborty R, Sarkar DC. A Novel Chiral Auxiliary for Enantioselective Synthesis of Tertiary Alcohol Synthetic Communications. 21: 1619-1624. DOI: 10.1080/00397919108021061 |
0.442 |
|
| 1991 |
Ranu BC, Das AR. Silica gel-supported zinc borohydride. 2. Regioselective 1,2-reduction of conjugated ketones and aldehydes to the corresponding allylic alcohols The Journal of Organic Chemistry. 56: 4796-4798. DOI: 10.1021/Jo00015A042 |
0.692 |
|
| 1991 |
Ranu BC, Basu MK. Stereocontrolled construction of angularly functionalized trans-fused cycloheptanoids via α-hydroxycyclobutane rearrangement followed by retroaldol cleavage Tetrahedron Letters. 32: 4177-4178. DOI: 10.1016/S0040-4039(00)79897-2 |
0.453 |
|
| 1991 |
Ranu BC, Basu MK. Use of zinc borohydride for efficient reduction of carboxylic ester to alcohol. Seleclive reduction of aliphatic ester in presence of aromatic ester under sonication Tetrahedron Letters. 32: 3243-3246. DOI: 10.1016/S0040-4039(00)79734-6 |
0.442 |
|
| 1991 |
Ranu BC, Bhar S, Sarkar DC. Surface-mediated solid phase michael reaction: dramatic acceleration on alumina Tetrahedron Letters. 32: 2811-2812. DOI: 10.1016/0040-4039(91)85093-K |
0.487 |
|
| 1991 |
Ranu BC, Chakraborty R. Highly selective reduction of conjugated nitroalkenes with zinc borohydride in DME Tetrahedron Letters. 32: 3579-3582. DOI: 10.1016/0040-4039(91)80839-X |
0.492 |
|
| 1990 |
Ranu BC, Chakraborty R. Ion exchange resin-mediated hydrolytic cleavage of epoxides simple one-pot synthesis of 2-arylketones from 1-aryl-1,2-epoxides Synthetic Communications. 20: 1751-1756. DOI: 10.1080/00397919008053099 |
0.423 |
|
| 1990 |
Ranu BC, Das AR. Regio- and stereo-selective reductive cleavage of epoxides with zinc borohydride supported on silica gel Journal of the Chemical Society, Chemical Communications. 1334-1335. DOI: 10.1039/C39900001334 |
0.496 |
|
| 1990 |
Sarkar DC, Das AR, Ranu BC. Use of zinc borohydride as an efficient and highly selective reducing agent. Selective reduction of ketones and conjugated aldehydes over conjugated enones The Journal of Organic Chemistry. 55: 5799-5801. DOI: 10.1021/Jo00309A028 |
0.69 |
|
| 1990 |
Ranu BC, Chakraborty R. Chemoselective reduction of aldehydes with zinc borohydride in tetrahydrofuran Tetrahedron Letters. 31: 7663-7664. DOI: 10.1016/S0040-4039(00)97326-X |
0.44 |
|
| 1989 |
Basu MK, Sarkar DC, Ranu BC. A mild and Selective Method of Ester Hydrolysis Synthetic Communications. 19: 627-631. DOI: 10.1080/00397918908050708 |
0.502 |
|
| 1989 |
Chakraborti R, Ranu BC, Ghatak UR. CHEMOSELECTIVE CATALYTIC HYDROGENATION OF CARBONYL CONJUGATED DOUBLE BONDS IN THE PRESENCE OF STYRENOID BONDS IN BICYCLO[3.3.1]NONADIENONES Organic Preparations and Procedures International. 21: 377-380. DOI: 10.1080/00304948909356405 |
0.694 |
|
| 1989 |
Ranu BC, Sarkar DC, Basu MK. A simple and efficient route towards usefully functionalised six and seven-membered ring systems via α-hydroxycyclobutane rearrangement followed by retroaldol cleavage Tetrahedron. 45: 3107-3114. DOI: 10.1016/S0040-4020(01)80137-X |
0.467 |
|
| 1989 |
BASU MK, SARKAR DC, RANU BC. ChemInform Abstract: A Mild and Selective Method of Ester Hydrolysis. Cheminform. 20. DOI: 10.1002/chin.198951104 |
0.33 |
|
| 1989 |
CHAKRABORTI R, RANU BC, GHATAK UR. ChemInform Abstract: Chemoselective Catalytic Hydrogenation of Carbonyl-Conjugated Double Bonds in the Presence of Styrenoid Bonds in Bicyclo(3.3.1)nonadienones. Cheminform. 20. DOI: 10.1002/chin.198947173 |
0.677 |
|
| 1989 |
RANU BC, SARKAR DC, BASU MK. ChemInform Abstract: A Simple and Efficient Route Toward Usefully Functionalized Six- and Seven-Membered Ring Systems via α-Hydroxycyclobutane Rearrangement Followed by Retroaldol Cleavage. Cheminform. 20. DOI: 10.1002/chin.198937141 |
0.364 |
|
| 1988 |
Ranu BC, Chakraborti R, Ghatak UR. A formylation–cyclisation method of synthesis of cycloalkenones from unsaturated ketones. Part 3. Simple synthesis of some functionalised angularly fused cyclopentenone and cyclopentanone derivatives Journal of the Chemical Society-Perkin Transactions 1. 795-801. DOI: 10.1039/P19880000795 |
0.767 |
|
| 1988 |
Ranu BC, Sarkar DC. A simple entry to functionalised seven-membered ring systems viaα-hydroxycyclobutane rearrangement followed by retroaldol cleavage Journal of the Chemical Society, Chemical Communications. 245-246. DOI: 10.1039/C39880000245 |
0.494 |
|
| 1988 |
Ranu BC, Sarkar DC. A simple, efficient, and highly selective method for the regeneration of carbonyl compounds from oximes and semicarbazones The Journal of Organic Chemistry. 53: 878-879. DOI: 10.1021/Jo00239A038 |
0.419 |
|
| 1988 |
Patra A, Mandal TK, Mukhopadhyay PK, Ranu BC. (+)-3′,4′-dihydrostephasubine, a bisbenzylisoquinoline alkaloid from Stephania hernandifolia Phytochemistry. 27: 653-655. DOI: 10.1016/0031-9422(88)83171-6 |
0.345 |
|
| 1988 |
RANU BC, CHAKRABORTI R, GHATAK UR. ChemInform Abstract: A Formylation-Cyclization Method of Synthesis of Cycloalkenones from Unsaturated Ketones. Part 3. Simple Synthesis of Some Functionalized Angularly Fused Cyclopentenone and Cyclopentanone Derivatives. Cheminform. 19. DOI: 10.1002/chin.198830091 |
0.743 |
|
| 1988 |
RANU BC, SARKAR DC. ChemInform Abstract: A Simple, Efficient, and Highly Selective Method for the Regeneration of Carbonyl Compounds from Oximes and Semicarbazones. Cheminform. 19. DOI: 10.1002/chin.198830081 |
0.341 |
|
| 1988 |
CHAKRABORTI R, RANU BC, GHATAK UR. ChemInform Abstract: Stereospecific Synthesis of endo-6-Aryl-2-oxobicyclo(3.3.1)nonanes. Cheminform. 19. DOI: 10.1002/chin.198816161 |
0.751 |
|
| 1987 |
Chakraborti R, Ranu BC, Ghatak UR. Stereospecific Synthesis ofEndo-6-Aryl-2-Oxobicyclo [3.3.1]Nonanes Synthetic Communications. 17: 1539-1543. DOI: 10.1080/00397918708057783 |
0.704 |
|
| 1987 |
Ranu BC, Sarkar DC. A Simple Synthesis of γ-Hydroxy-α β-Unsaturated Aldehydes Synthetic Communications. 17: 155-160. DOI: 10.1080/00397918708057215 |
0.448 |
|
| 1987 |
Hudlicky T, Sinai-Zingde G, Natchus M, Ranu B, Papadopolous P. System oriented design of triquinanes: stereocontrolled synthesis of pentalenic acid and pentalenene Tetrahedron. 43: 5685-5721. DOI: 10.1016/S0040-4020(01)87747-4 |
0.576 |
|
| 1987 |
RANU BC, SARKER DC. ChemInform Abstract: A Simple Synthesis of γ-Hydroxy-α,β-Unsaturated Aldehydes. Cheminform. 18. DOI: 10.1002/chin.198745124 |
0.372 |
|
| 1986 |
Hudlicky T, Kwart LD, Tiedje MH, Ranu BC, Short RP, Frazier JO, Rigby HL. General Methodology for the Topologically Selective Preparation of Linear and Nonlinear Tricyclopentanoids of Hirsutane and Isocomene Typeviaa Claisen Rearrangement / Cyclopentene Annulation Sequence. Total Synthesis of (±)- Epiisocomene Synthesis. 1986: 716-727. DOI: 10.1055/S-1986-31756 |
0.612 |
|
| 1985 |
Chakraborti R, Ranu BC, Ghatak UR. A formylation-cyclization method of synthesis of cycloalkenones from unsaturated ketones. 2. Simple synthesis of some functionalized bicyclo[3.3.1]nonane derivatives The Journal of Organic Chemistry. 50: 5268-5271. DOI: 10.1021/Jo00225A054 |
0.755 |
|
| 1985 |
Hudlicky T, Ranu BC, Naqvi SM, Srnak A. Intramolecular Simmons-Smith reaction and other synthetic alternatives to cyclopropanation of dienic diazo ketones. Parallel decomposition pathways of a sterically congested diazo ketone and its vinylcyclopropane under thermal, photolytic, acid-catalyzed, and radical-release conditions The Journal of Organic Chemistry. 50: 123-127. DOI: 10.1021/Jo00201A026 |
0.624 |
|
| 1985 |
HUDLICKY T, RANU BC, NAQVI SM, SRNAK A. ChemInform Abstract: INTRAMOLECULAR SIMMONS-SMITH REACTION AND OTHER SYNTHETIC ALTERNATIVES TO CYCLOPROPANATION OF DIENIC DIAZO KETONES. PARALLEL DECOMPOSITION PATHWAYS OF A STERICALLY CONGESTED DIAZO KETONE AND ITS VINYLCYCLOPROPANE UNDER THERMAL, PHOTOL Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198522135 |
0.633 |
|
| 1984 |
Ranu BC, Kavka M, Higgs LA, Hudlickyl T. Stereocontrolled total synthesis of isocomene sesquiterpenes Tetrahedron Letters. 25: 2447-2450. DOI: 10.1016/S0040-4039(01)81201-6 |
0.463 |
|
| 1984 |
SHORT RP, REVOL J, RANU BC, HUDLICKY T. ChemInform Abstract: GENERAL METHOD OF SYNTHESIS OF CYCLOPENTANOID TERPENIC ACIDS. STEREOCONTROLLED TOTAL SYNTHESES OF (.+-.)-ISOCOMENIC ACID AND (.+-.)-EPIISOCOMENIC ACID Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198420288 |
0.522 |
|
| 1983 |
Short RP, Revol JM, Ranu BC, Hudlicky T. General method of synthesis of cyclopentanoid terpenic acids. Stereocontrolled total syntheses of (.+-.)-isocomenic acid and (.+-.)-epiisocomenic acid The Journal of Organic Chemistry. 48: 4453-4461. DOI: 10.1021/Jo00172A003 |
0.631 |
|
| 1983 |
GUPTA RD, RANU BC, GHATAK UR. ChemInform Abstract: A Highly Efficient Synthesis of Functionalised Bridged-Cycloalkenones from γ,δ-Unsaturated Methyl Ketones by a Modified Formylation-Cyclisation Route. Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198352150 |
0.737 |
|
| 1982 |
Ranu BC, Sarkar M, Chakraborti PC, Ghatak UR. Synthetic studies directed towards complex diterpenoids. Part 15. Synthesis and stereochemistry of the catalytic reduction of Δ4b(5)-gibbenes and related compounds Journal of the Chemical Society-Perkin Transactions 1. 13: 865-873. DOI: 10.1039/P19820000865 |
0.755 |
|
| 1982 |
RANU BC, SARKAR M, CHAKRABORTI PC, GHATAK UR. ChemInform Abstract: SYNTHETIC STUDIES DIRECTED TOWARDS COMPLEX DITERPENOIDS. PART 15. SYNTHESIS AND STEREOCHEMISTRY OF THE CATALYTIC REDUCTION OF Δ4B(5)-GIBBENES AND RELATED COMPOUNDS Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198224195 |
0.715 |
|
| 1977 |
Wenkert E, Goodwin TE, Ranu BC. .gamma.-Alkylation of .alpha.,.beta.-unsaturated carbonyl compounds The Journal of Organic Chemistry. 42: 2137-2141. DOI: 10.1021/Jo00432A026 |
0.349 |
|
| 1977 |
WENKERT E, GOODWIN TE, RANU BC. ChemInform Abstract: Γ-ALKYLATION OF α,β-UNSATURATED CARBONYL COMPOUNDS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197741190 |
0.333 |
|
| 1977 |
Wenkert E, Goodwin TE, Ranu BC. γ-Alkylation of α/β-unsaturated carbonyl compounds Journal of Organic Chemistry. 42: 2137-2141. DOI: 10.1002/Chin.197741190 |
0.659 |
|
| 1976 |
Ghatak UR, Alam SK, Chakraborti PC, Ranu BC. Condensed cyclic and bridged-ring systems. Part IV. Stereochemically controlled synthesis of some endo-2-aryl-6-oxobicyclo[3.2.1]octanes and related compounds through intramolecular alkylations of γδ-unsaturated α′-diazomethyl ketones Journal of the Chemical Society-Perkin Transactions 1. 7: 1669-1673. DOI: 10.1039/P19760001669 |
0.762 |
|
| 1976 |
GHATAK UR, ALAM SK, CHAKRABORTI PC, RANU BC. ChemInform Abstract: CONDENSED CYCLIC AND BRIDGED-RING SYSTEMS. PART IV. STEREOCHEMICALLY CONTROLLED SYNTHESIS OF SOME ENDO-2-ARYL-6-OXOBICYCLO(3.2.1)OCTANES AND RELATED COMPOUNDS THROUGH INTRAMOLECULAR ALKYLATIONS OF ΓΔ-UNSATURATED α′-DIAZOMETHYL KETONES Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/chin.197649181 |
0.726 |
|
| 1973 |
GHATAK UR, CHAKRABORTI PC, RANU BC, SANYAL B. ChemInform Abstract: INTRAMOLECULAR KETO-CARBENOID ADDITION TO DOUBLE BONDS, STEREOCHEMISTRY OF THE CATALYTIC REDUCTION OF DELTA(9(11))-GIBBENES AND RELATED COMPOUNDS Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197344266 |
0.761 |
|
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