| Year |
Citation |
Score |
| 2023 |
Hanchate V, Reddy SN, Kumar A, Prabhu KR. Divergent reactivity of sulfoxonium ylide with allyl carbonate and allyl carbamate. Chemical Communications (Cambridge, England). PMID 37417209 DOI: 10.1039/d3cc01657a |
0.795 |
|
| 2023 |
Manna S, Prabhu KR. Visible-Light-Mediated Vicinal Difunctionalization of Activated Alkynes with Boronic Acids: Substrate-Controlled Rapid Access to 3-Alkylated Coumarins and Unsaturated Spirocycles. Organic Letters. PMID 36706367 DOI: 10.1021/acs.orglett.2c04333 |
0.659 |
|
| 2021 |
Kumar A, Hanchate V, Prabhu KR. Rhodium(III)-Catalyzed Cascade Reactions of Imines/Imidates with 4-Hydroxy-2-alkynoates to Synthesize Regioselective Furanone-Fused Isoquinoline Scaffolds. The Journal of Organic Chemistry. 86: 17965-17974. PMID 34843247 DOI: 10.1021/acs.joc.1c02300 |
0.814 |
|
| 2021 |
Sherikar MS, Bettadapur KR, Lanke V, Prabhu KR. Rhodium(iii)-catalyzed synthesis of trisubstituted furans via vinylic C-H bond activation. Organic & Biomolecular Chemistry. 19: 7470-7474. PMID 34612365 DOI: 10.1039/d1ob01293b |
0.822 |
|
| 2021 |
Kumar A, Prabhu KR. Rhodium(III)-catalyzed [5+1] annulation of 2-alkenylphenols with maleimides: access to highly functionalized spirocyclic skeletons. Chemical Communications (Cambridge, England). PMID 34313254 DOI: 10.1039/d1cc01758f |
0.365 |
|
| 2021 |
Panigrahi A, Muniraj N, Prabhu KR. -Triflination of pyrazolones: a new method for N-S bond formation. Organic & Biomolecular Chemistry. 19: 5534-5538. PMID 34105585 DOI: 10.1039/d1ob00862e |
0.618 |
|
| 2021 |
Sherikar MS, Devarajappa R, Prabhu KR. Dual Role of the Rhodium(III) Catalyst in C-H Activation: [4 + 3] Annulation of Amide with Allylic Alcohols to 7-Membered Lactams. The Journal of Organic Chemistry. PMID 33689338 DOI: 10.1021/acs.joc.1c00048 |
0.832 |
|
| 2020 |
Manna S, Someswara Ashwathappa PK, Prabhu KR. Visible light-mediated -annulation of activated alkynes: access to 3-alkylated spiro[4,5]-trienones, thiaspiro[4,5]-trienones and azaspiro[4,5]-trienones. Chemical Communications (Cambridge, England). PMID 33016280 DOI: 10.1039/D0Cc01217C |
0.667 |
|
| 2020 |
Hanchate V, Devarajappa R, Prabhu KR. Sulfoxonium-Ylide-Directed C-H Activation and Tandem (4 + 1) Annulation. Organic Letters. PMID 32227971 DOI: 10.1021/Acs.Orglett.0C00451 |
0.823 |
|
| 2020 |
Sherikar MS, Devarajappa R, Prabhu KR. Weak Coordinating Carbonyl-Directed Rhodium(III)-Catalyzed C-H Activation at the C4-Position of Indole with Allyl Alcohols. The Journal of Organic Chemistry. PMID 32192332 DOI: 10.1021/Acs.Joc.0C00277 |
0.832 |
|
| 2020 |
Kumar A, Prabhu KR. Rhodium(III)-Catalyzed C-H Activation: A Cascade Approach for the Regioselective Synthesis of Fused Heterocyclic Lactone Scaffolds. The Journal of Organic Chemistry. PMID 31994394 DOI: 10.1021/Acs.Joc.9B03266 |
0.514 |
|
| 2020 |
Bhat K S, Lanke V, Prasad JD, Prabhu KR. Ligand-free Suzuki coupling reaction with highly recyclable ionic palladium catalyst, Ti1-xPdxO2-x (x = 0.03) Applied Catalysis a: General. 596: 117516. DOI: 10.1016/J.Apcata.2020.117516 |
0.779 |
|
| 2020 |
Panigrahi A, Muniraj N, Prabhu KR. Iodine promoted One‐Pot Multicomponent Chemoselective Reaction for C‐C/C‐N and C‐C/C‐S Bond Formation using Thiols at Room Temperature European Journal of Organic Chemistry. 2020: 5780-5784. DOI: 10.1002/Ejoc.202000993 |
0.654 |
|
| 2020 |
Panigrahi A, Dhineshkumar J, Prabhu KR. Iodine‐Catalyzed C−H Functionalization of Cyclopentenedione with Benzamidine: A Double Dehydrogenative Oxidative Cyclization to Access Fused Imidazoles Advanced Synthesis & Catalysis. 362: 2466-2473. DOI: 10.1002/Adsc.202000347 |
0.807 |
|
| 2019 |
Hanchate V, Kumar A, Prabhu KR. Synthesis of Naphthols by Rh(III)-Catalyzed Domino C-H Activation, Annulation, and Lactonization Using Sulfoxonium Ylide as a Traceless Directing Group. Organic Letters. PMID 31596098 DOI: 10.1021/Acs.Orglett.9B03182 |
0.819 |
|
| 2019 |
Hanchate V, Kumar A, Prabhu KR. Synthesis of Furanone Fused 1,2-Benzothiazine by Rh(III)-Catalyzed C-H Activation: Regioselective Oxidative-Annulation leading to in situ Lactonization in One-Pot. The Journal of Organic Chemistry. PMID 31397567 DOI: 10.1021/Acs.Joc.9B01899 |
0.824 |
|
| 2019 |
Sherikar MS, Prabhu KR. Weak Coordinating Carboxylate Directed Rhodium(III)-Catalyzed C-H Activation: Switchable Decarboxylative Heck-Type and [4 + 1] Annulation Reactions with Maleimides. Organic Letters. PMID 31180229 DOI: 10.1021/Acs.Orglett.9B01412 |
0.834 |
|
| 2019 |
Hanchate V, Muniraj N, Prabhu KR. Rh(III)-Catalyzed Oxidative Annulation of Sulfoximines with Arylalkynyl Silanes via Desilylation. The Journal of Organic Chemistry. PMID 31117563 DOI: 10.1021/Acs.Joc.9B00743 |
0.814 |
|
| 2019 |
Manna S, Prabhu KR. Visible light-mediated Direct Decarboxylative Acylation of Electron Deficient Heteroarenes using α-Ketoacids. The Journal of Organic Chemistry. PMID 30933509 DOI: 10.1021/Acs.Joc.9B00004 |
0.656 |
|
| 2019 |
Muniraj N, Prabhu KR. Cobalt(III)-Catalyzed [4 + 2] Annulation of N-Chlorobenzamides with Maleimides. Organic Letters. PMID 30689392 DOI: 10.1021/acs.orglett.8b04117 |
0.327 |
|
| 2019 |
Kumar A, Muniraj N, Prabhu KR. Cobalt(III)-Catalyzed Direct ortho
-Alkenylation of Arylpyrazoles: A Comparative Study on Decarboxylation and Desilylation European Journal of Organic Chemistry. 2019: 2735-2739. DOI: 10.1002/EJOC.201900270 |
0.303 |
|
| 2019 |
Rao S, Ashwathappa PKS, Prabhu KR. Boron-Catalyzed Carbonate Functionality Transfer Reaction Asian Journal of Organic Chemistry. 8: 320-323. DOI: 10.1002/Ajoc.201800751 |
0.713 |
|
| 2019 |
Muniraj N, Kumar A, Prabhu KR. Cobalt‐Catalyzed Regioselective [4+2] Annulation/Lactonization of Benzamides with 4‐Hydroxy‐2‐Alkynoates under Aerobic Conditions Advanced Synthesis & Catalysis. 362: 152-159. DOI: 10.1002/Adsc.201901119 |
0.32 |
|
| 2019 |
Kumar A, Muniraj N, Prabhu KR. Manganese‐Catalysed C−H Activation: A Regioselective C−H Alkenylation of Indoles and other (hetero)aromatics with 4‐Hydroxy‐2‐Alkynoates Leading to Concomitant Lactonization Advanced Synthesis & Catalysis. 361: 4933-4940. DOI: 10.1002/Adsc.201900678 |
0.376 |
|
| 2019 |
Rao S, Kapanaiah R, Prabhu KR. Boron‐Catalyzed C−C Functionalization of Allyl Alcohols Advanced Synthesis & Catalysis. 361: 1301-1306. DOI: 10.1002/Adsc.201801389 |
0.713 |
|
| 2018 |
Siddaraju Y, Prabhu KR. Iodine-Catalyzed Chemoselective Hydroamination Reaction Using 5-Mercaptotetrazoles Derivatives. Acs Omega. 3: 4908-4917. PMID 31458707 DOI: 10.1021/acsomega.8b00499 |
0.833 |
|
| 2018 |
Rao S, Joy MN, Prabhu KR. Employing Water as the Hydride Source in Synthesis: A Case Study of Diboron Mediated Alkyne Hydroarylation. The Journal of Organic Chemistry. PMID 30365320 DOI: 10.1021/Acs.Joc.8B01965 |
0.722 |
|
| 2018 |
Hande AE, Ramesh VB, Prabhu KR. Rh(iii)-Catalyzed ortho-C-(sp)-H amidation of ketones and aldehydes under synergistic ligand-accelerated catalysis. Chemical Communications (Cambridge, England). 54: 12113-12116. PMID 30302452 DOI: 10.1039/C8Cc07006G |
0.848 |
|
| 2018 |
Sherikar MS, Kapanaiah R, Lanke V, Prabhu KR. Rhodium(iii)-catalyzed C-H activation at the C4-position of indole: switchable hydroarylation and oxidative Heck-type reactions of maleimides. Chemical Communications (Cambridge, England). 54: 11200-11203. PMID 30229766 DOI: 10.1039/C8Cc06264A |
0.823 |
|
| 2018 |
Siddaraju Y, Prabhu KR. Iodine-Catalyzed Chemoselective C-N Bond-Forming Reactions Using Benzylic or Cinnamyl Alcohols with Heterocyclic Thiols and Thiones. The Journal of Organic Chemistry. PMID 30032620 DOI: 10.1021/Acs.Joc.8B01745 |
0.827 |
|
| 2018 |
Prabhu KR, Rao S. Stereodivergent Alkyne Reduction Using Water as the Hydrogen Source. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29957845 DOI: 10.1002/Chem.201803147 |
0.738 |
|
| 2018 |
Siddaraju Y, Prabhu KR. Regioselective Sulfenylation of α'-CHor α'-CHGroups of α,β-Unsaturated Ketones with Heterocyclic Thiols. The Journal of Organic Chemistry. 83: 2986-2992. PMID 29389131 DOI: 10.1021/Acs.Joc.7B03290 |
0.782 |
|
| 2018 |
Bettadapur KR, Kapanaiah R, Lanke V, Prabhu KR. Weak Directing Group Steered Formal Oxidative [2+2+2]-Cyclization for Selective Benzannulation of Indoles. The Journal of Organic Chemistry. 83: 1810-1818. PMID 29384377 DOI: 10.1021/Acs.Joc.7B02719 |
0.83 |
|
| 2018 |
Dhineshkumar J, Gadde K, Prabhu KR. Substituent-Directed Regioselective Azidation: Copper-Catalyzed C-H Azidation and Iodine-Catalyzed Dearomatizative Azidation of Indole. The Journal of Organic Chemistry. 83: 228-235. PMID 29205046 DOI: 10.1021/Acs.Joc.7B02591 |
0.842 |
|
| 2018 |
Bettadapur KR, Sherikar MS, Lanke V, Prabhu KR. RhIII
-Catalyzed C−H Activation: Mizoroki-Heck-Type Reaction of Maleimides Asian Journal of Organic Chemistry. 7: 1338-1342. DOI: 10.1002/Ajoc.201800193 |
0.82 |
|
| 2018 |
Muniraj N, Prabhu KR. Cobalt(III)-Catalyzed C−H Activation: Counter Anion Triggered Desilylative Direct ortho-
Vinylation of Secondary Benzamides Advanced Synthesis & Catalysis. 360: 3579-3584. DOI: 10.1002/Adsc.201800649 |
0.394 |
|
| 2018 |
Muniraj N, Prabhu KR. Cobalt(III)−Catalyzed C−H Activation: A Secondary Amide Directed Decarboxylative Functionalization of Alkynyl Carboxylic Acids Wherein Amide NH-group Remains Unreactive Advanced Synthesis & Catalysis. 360: 1370-1375. DOI: 10.1002/Adsc.201701406 |
0.361 |
|
| 2017 |
Dhineshkumar J, Samaddar P, Prabhu KR. Catalyst-Free Cross-Dehydrogenative Coupling Strategy Using Air as an Oxidant: Synthesis of α-Aminophosphonates. Acs Omega. 2: 4885-4893. PMID 31457767 DOI: 10.1021/acsomega.7b00881 |
0.823 |
|
| 2017 |
Muniraj N, Prabhu KR. Co(III)-Catalyzed C-H Activation: A Site-Selective Conjugate Addition of Maleimide to Indole at the C-2 Position. Acs Omega. 2: 4470-4479. PMID 31457739 DOI: 10.1021/acsomega.7b00870 |
0.381 |
|
| 2017 |
Hande AE, Prabhu KR. Ru(II)-Catalyzed C-H Amidation of Indoline at the C7-Position Using Dioxazolone as an Amidating Agent: Synthesis of 7-Amino Indoline Scaffold. The Journal of Organic Chemistry. 82: 13405-13413. PMID 29134809 DOI: 10.1021/Acs.Joc.7B02500 |
0.83 |
|
| 2017 |
Varun BV, Prabhu KR. Sulfur Assisted Tandem Electrophilic Fluorinative Deacylation: Synthesis of α-Fluoro β-Ketosulfides. The Journal of Organic Chemistry. PMID 28786672 DOI: 10.1021/Acs.Joc.7B01547 |
0.351 |
|
| 2017 |
Siddaraju Y, Prabhu KR. Iodine-catalyzed sulfenylation of pyrazolones using dimethyl sulfoxide as an oxidant. Organic & Biomolecular Chemistry. 15: 5191-5196. PMID 28590497 DOI: 10.1039/C7Ob00561J |
0.826 |
|
| 2017 |
Muniraj N, Prabhu KR. Cobalt(III)-Catalyzed C-H Activation: Azo Directed Selective 1,4-Addition of Ortho C-H Bond to Maleimides. The Journal of Organic Chemistry. 82: 6913-6921. PMID 28560875 DOI: 10.1021/Acs.Joc.7B01094 |
0.498 |
|
| 2017 |
Bettadapur KR, Lanke V, Prabhu KR. A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides. Chemical Communications (Cambridge, England). 53: 6251-6254. PMID 28540938 DOI: 10.1039/C7Cc02392H |
0.811 |
|
| 2017 |
Lanke V, Prabhu KR. Iridium(iii) catalyzed regioselective amidation of indoles at the C4-position using weak coordinating groups. Chemical Communications (Cambridge, England). 53: 5117-5120. PMID 28435947 DOI: 10.1039/C7Cc00763A |
0.804 |
|
| 2017 |
Ojha DP, Gadde K, Prabhu KR. Pd-Boron-Catalyzed One Carbon Isomerization of Olefins: Water Assisted Process at Room Temperature. The Journal of Organic Chemistry. 82: 4859-4865. PMID 28402642 DOI: 10.1021/Acs.Joc.7B00580 |
0.806 |
|
| 2017 |
Siddaraju Y, Prabhu KR. Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: Sulfenylation of Enaminones Using Dimethyl Sulfoxide as an Oxidant. The Journal of Organic Chemistry. 82: 3084-3093. PMID 28229592 DOI: 10.1021/Acs.Joc.7B00073 |
0.831 |
|
| 2017 |
Rao S, Prabhu KR. Gold-Catalyzed [2,3]-Sigmatropic Rearrangement: Reaction of Aryl Allyl Alcohols with Diazo Compounds. Organic Letters. PMID 28170278 DOI: 10.1021/Acs.Orglett.6B03836 |
0.759 |
|
| 2017 |
Varun BV, Dhineshkumar J, Bettadapur KR, Siddaraju Y, Alagiri K, Prabhu KR. Recent advancements in dehydrogenative cross coupling reactions for CC bond formation Tetrahedron Letters. 58: 803-824. DOI: 10.1016/J.Tetlet.2017.01.035 |
0.795 |
|
| 2017 |
Hande AE, Muniraj N, Prabhu KR. Cobalt(III)-Catalyzed C-H Amidation of Azobenzene Derivatives Using Dioxazolone as an Amidating Reagent Chemistryselect. 2: 5965-5969. DOI: 10.1002/SLCT.201701277 |
0.334 |
|
| 2016 |
Siddaraju Y, Prabhu KR. Iodine Promoted Regioselective α-Sulfenylation of Carbonyl Compounds using Dimethyl Sulfoxide as an Oxidant. Organic Letters. 18: 6090-6093. PMID 27934388 DOI: 10.1021/Acs.Orglett.6B03084 |
0.81 |
|
| 2016 |
Lanke V, Bettadapur KR, Prabhu KR. Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles. Organic Letters. 18: 5496-5499. PMID 27736082 DOI: 10.1021/Acs.Orglett.6B02698 |
0.797 |
|
| 2016 |
Ojha DP, Gadde K, Prabhu KR. Generation of Hydrogen from Water: A Pd-Catalyzed Reduction of Water Using Diboron Reagent at Ambient Conditions. Organic Letters. 18: 5062-5065. PMID 27617623 DOI: 10.1021/Acs.Orglett.6B02508 |
0.792 |
|
| 2016 |
Dhineshkumar J, Samaddar P, Prabhu KR. A copper catalyzed azidation and peroxidation of β-naphthols via an oxidative dearomatization strategy. Chemical Communications (Cambridge, England). PMID 27545203 DOI: 10.1039/c6cc04894c |
0.828 |
|
| 2016 |
Siddaraju Y, Prabhu KR. Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: A Regioselective Sulfenylation of Imidazoheterocycles Using Dimethyl Sulfoxide as an Oxidant. The Journal of Organic Chemistry. 81: 7838-46. PMID 27490357 DOI: 10.1021/Acs.Joc.6B01487 |
0.844 |
|
| 2016 |
Varun BV, Gadde K, Prabhu KR. Synthesis of α-sulfenyl monoketones via a metal-free oxidative cross dehydrogenative coupling (CDC) reaction. Organic & Biomolecular Chemistry. PMID 27452676 DOI: 10.1039/c6ob01243d |
0.807 |
|
| 2016 |
Keshri P, Bettadapur KR, Lanke V, Prabhu KR. Ru(II)-Catalyzed C-H Activation: Amide-Directed 1,4-Addition of the Ortho C-H Bond to Maleimides. The Journal of Organic Chemistry. 81: 6056-65. PMID 27314834 DOI: 10.1021/Acs.Joc.6B01160 |
0.836 |
|
| 2016 |
Ojha DP, Prabhu KR. Pd-Catalyzed Hydroborylation of Alkynes: A Ligand Controlled Regioselectivity Switch for the Synthesis of α- or β-Vinylboronates. Organic Letters. 18: 432-5. PMID 26760916 DOI: 10.1021/Acs.Orglett.5B03416 |
0.778 |
|
| 2016 |
Siddaraju Y, Prabhu KR. Transition metal-free Minisci reaction promoted by NCS, and TBHP: acylation of heteroarenes Tetrahedron. 72: 959-967. DOI: 10.1016/J.Tet.2015.12.065 |
0.815 |
|
| 2016 |
Muniraj N, Dhineshkumar J, Prabhu KR. N-Iodosuccinimide Catalyzed Oxidative Selenocyanation and Thiocyanation of Electron Rich Arenes Chemistryselect. 1: 1033-1038. DOI: 10.1002/SLCT.201600292 |
0.784 |
|
| 2016 |
Muniraj N, Dhineshkumar J, Prabhu KR. ChemInform Abstract: N-Iodosuccinimide Catalyzed Oxidative Selenocyanation and Thiocyanation of Electron Rich Arenes. Cheminform. 47. DOI: 10.1002/CHIN.201637157 |
0.787 |
|
| 2016 |
Siddaraju Y, Prabhu KR. ChemInform Abstract: Transition Metal-Free Minisci Reaction Promoted by NCS, and TBHP: Acylation of Heteroarenes. Cheminform. 47. DOI: 10.1002/CHIN.201624167 |
0.783 |
|
| 2016 |
Dhineshkumar J, Prabhu KR. ChemInform Abstract: An Efficient Tertiary Azidation of 1,3-Dicarbonyl Compounds in Water Catalyzed by Tetrabutylammonium Iodide. Cheminform. 47. DOI: 10.1002/CHIN.201623088 |
0.781 |
|
| 2015 |
Siddaraju Y, Prabhu KR. A chemoselective α-aminoxylation of aryl ketones: a cross dehydrogenative coupling reaction catalysed by Bu4NI. Organic & Biomolecular Chemistry. 13: 11651-6. PMID 26467572 DOI: 10.1039/C5Ob01929J |
0.818 |
|
| 2015 |
Bettadapur KR, Lanke V, Prabhu KR. Ru (II)-Catalyzed C-H Activation: Ketone-Directed Novel 1,4-Addition of Ortho C-H Bond to Maleimides. Organic Letters. 17: 4658-61. PMID 26348371 DOI: 10.1021/Acs.Orglett.5B01810 |
0.837 |
|
| 2015 |
Lanke V, Bettadapur KR, Prabhu KR. Site-Selective Addition of Maleimide to Indole at the C-2 Position: Ru(II)-Catalyzed C-H Activation. Organic Letters. 17: 4662-5. PMID 26348254 DOI: 10.1021/Acs.Orglett.5B01809 |
0.821 |
|
| 2015 |
Varun BV, Gadde K, Prabhu KR. Sulfenylation of β-Diketones Using C-H Functionalization Strategy. Organic Letters. 17: 2944-7. PMID 26053524 DOI: 10.1021/acs.orglett.5b01221 |
0.753 |
|
| 2015 |
Siddaraju Y, Prabhu KR. Iodine promoted α-hydroxylation of ketones. Organic & Biomolecular Chemistry. 13: 6749-53. PMID 25997701 DOI: 10.1039/C5Ob00684H |
0.788 |
|
| 2015 |
Ojha DP, Prabhu KR. Regioselective synthesis of vinyl halides, vinyl sulfones, and alkynes: a tandem intermolecular nucleophilic and electrophilic vinylation of tosylhydrazones. Organic Letters. 17: 18-21. PMID 25495804 DOI: 10.1021/Ol503114N |
0.787 |
|
| 2015 |
Dhineshkumar J, Prabhu KR. An Efficient Tertiary Azidation of 1,3-Dicarbonyl Compounds in Water Catalyzed by Tetrabutylammonium Iodide European Journal of Organic Chemistry. 2016: 447-452. DOI: 10.1002/EJOC.201501374 |
0.777 |
|
| 2015 |
Rokade BV, Gadde K, Prabhu KR. ChemInform Abstract: Copper-Catalyzed Direct Transformation of Secondary Allylic and Benzylic Alcohols into Azides and Amides: An Efficient Utility of Azide as a Nitrogen Source. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201533108 |
0.799 |
|
| 2014 |
Varun BV, Prabhu KR. Regioselective thiolation of arenes and heteroarenes: C-H functionalization strategy for C-S bond formation. The Journal of Organic Chemistry. 79: 9655-68. PMID 25296156 DOI: 10.1021/jo501793q |
0.412 |
|
| 2014 |
Rokade BV, Prabhu KR. Copper-catalyzed decarboxylative sulfonylation of α,β-unsaturated carboxylic acids. The Journal of Organic Chemistry. 79: 8110-7. PMID 25098975 DOI: 10.1021/Jo501314Y |
0.802 |
|
| 2014 |
Siddaraju Y, Lamani M, Prabhu KR. A transition metal-free Minisci reaction: acylation of isoquinolines, quinolines, and quinoxaline. The Journal of Organic Chemistry. 79: 3856-65. PMID 24734905 DOI: 10.1021/Jo500294Z |
0.829 |
|
| 2014 |
Varun BV, Sood A, Prabhu KR. A metal-free and a solvent-free synthesis of thio-amides and amides: an efficient Friedel–Crafts arylation of isothiocyanates and isocyanates Rsc Adv.. 4: 60798-60807. DOI: 10.1039/C4Ra12944J |
0.406 |
|
| 2014 |
Rokade BV, Gadde K, Prabhu KR. ChemInform Abstract: Copper-Catalyzed Oxidative Transformation of Secondary Alcohols to 1,5-Disubstituted Tetrazoles. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201435155 |
0.793 |
|
| 2013 |
Ojha DP, Prabhu KR. Pd-catalyzed cross-coupling reactions of hydrazones: regioselective synthesis of highly branched dienes. The Journal of Organic Chemistry. 78: 12136-43. PMID 24245793 DOI: 10.1021/Jo402153T |
0.799 |
|
| 2013 |
Dhineshkumar J, Prabhu KR. Cross-hetero-dehydrogenative coupling reaction of phosphites: a catalytic metal-free phosphorylation of amines and alcohols. Organic Letters. 15: 6062-5. PMID 24219013 DOI: 10.1021/ol402956b |
0.823 |
|
| 2013 |
Rokade BV, Prabhu KR. Synthesis of substituted nitroolefins: a copper catalyzed nitrodecarboxylation of unsaturated carboxylic acids. Organic & Biomolecular Chemistry. 11: 6713-6. PMID 24175324 DOI: 10.1039/C3Ob41408F |
0.825 |
|
| 2013 |
Lanke V, Prabhu KR. Highly regioselective C2-alkenylation of indoles using the N-benzoyl directing group: an efficient Ru-catalyzed coupling reaction. Organic Letters. 15: 2818-21. PMID 23701514 DOI: 10.1021/Ol4011486 |
0.795 |
|
| 2013 |
Dhineshkumar J, Lamani M, Alagiri K, Prabhu KR. A versatile C-H functionalization of tetrahydroisoquinolines catalyzed by iodine at aerobic conditions. Organic Letters. 15: 1092-5. PMID 23419035 DOI: 10.1021/Ol4001153 |
0.834 |
|
| 2013 |
Varun BV, Prabhu KR. A non-isothiocyanate route to synthesize trisubstituted thioureas of arylamines using in situ generated dithiocarbamates Rsc Advances. 3: 3079. DOI: 10.1039/C2Ra23257J |
0.412 |
|
| 2013 |
Dhineshkumar J, Prabhu KR. Correction to Cross-Hetero-Dehydrogenative Coupling Reaction of Phosphites: A Catalytic Metal-Free Phosphorylation of Amines and Alcohols Organic Letters. 16: 326-326. DOI: 10.1021/Ol403578P |
0.811 |
|
| 2012 |
Ojha DP, Prabhu KR. Palladium catalyzed coupling of tosylhydrazones with aryl and heteroaryl halides in the absence of external ligands: synthesis of substituted olefins. The Journal of Organic Chemistry. 77: 11027-33. PMID 23181970 DOI: 10.1021/Jo301987C |
0.826 |
|
| 2012 |
Lamani M, Prabhu KR. NIS-catalyzed reactions: amidation of acetophenones and oxidative amination of propiophenones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14638-42. PMID 23042487 DOI: 10.1002/Chem.201202703 |
0.827 |
|
| 2012 |
Lamani M, Guralamata RS, Prabhu KR. Guanidine catalyzed aerobic reduction: a selective aerobic hydrogenation of olefins using aqueous hydrazine. Chemical Communications (Cambridge, England). 48: 6583-5. PMID 22622254 DOI: 10.1039/C2Cc32611F |
0.801 |
|
| 2012 |
Rokade BV, Prabhu KR. Chemoselective Schmidt reaction mediated by triflic acid: selective synthesis of nitriles from aldehydes. The Journal of Organic Chemistry. 77: 5364-70. PMID 22616901 DOI: 10.1021/Jo3008258 |
0.817 |
|
| 2012 |
Rokade BV, Malekar SK, Prabhu KR. A novel oxidative transformation of alcohols to nitriles: an efficient utility of azides as a nitrogen source. Chemical Communications (Cambridge, England). 48: 5506-8. PMID 22540126 DOI: 10.1039/C2Cc31256E |
0.791 |
|
| 2012 |
Alagiri K, Devadig P, Prabhu KR. CDC reactions of N-aryl tetrahydroisoquinolines using catalytic amounts of DDQ: C-H activation under aerobic conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5160-4. PMID 22431410 DOI: 10.1002/Chem.201200100 |
0.455 |
|
| 2012 |
Lamani M, Devadig P, Prabhu KR. A non-metal catalysed oxidation of primary azides to nitriles at ambient temperature. Organic & Biomolecular Chemistry. 10: 2753-9. PMID 22371205 DOI: 10.1039/C2Ob06949K |
0.806 |
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| 2012 |
Alagiri K, Prabhu KR. C-H functionalization of tertiary amines by cross dehydrogenative coupling reactions: solvent-free synthesis of α-aminonitriles and β-nitroamines under aerobic condition. Organic & Biomolecular Chemistry. 10: 835-42. PMID 22130687 DOI: 10.1039/c1ob06466e |
0.369 |
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| 2012 |
Alagiri K, Devadig P, Prabhu KR. Molybdenum trioxide catalyzed oxidative cross-dehydrogenative coupling of benzylic sp3 C–H bonds: synthesis of α-aminophosphonates under aerobic conditions Tetrahedron Letters. 53: 1456-1459. DOI: 10.1016/J.TETLET.2012.01.031 |
0.311 |
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| 2012 |
Lamani M, Ravikumara GS, Prabhu KR. ChemInform Abstract: Iron(III) Chloride Catalyzed Aerobic Reduction of Olefins Using Aqueous Hydrazine at Ambient Temperature. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201240036 |
0.762 |
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| 2012 |
Alagiri K, Devadig P, Prabhu KR. ChemInform Abstract: Molybdenum Trioxide Catalyzed Oxidative Cross-Dehydrogenative Coupling of Benzylic sp3C-H Bonds: Synthesis of α-Aminophosphonates under Aerobic Conditions. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201228177 |
0.343 |
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| 2012 |
Lamani M, Ravikumara GS, Prabhu KR. Iron(III) Chloride-Catalysed Aerobic Reduction of Olefins using Aqueous Hydrazine at Ambient Temperature Advanced Synthesis & Catalysis. 354: 1437-1442. DOI: 10.1002/Adsc.201200110 |
0.802 |
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| 2011 |
Alagiri K, Kumara GS, Prabhu KR. An oxidative cross-dehydrogenative-coupling reaction in water using molecular oxygen as the oxidant: vanadium catalyzed indolation of tetrahydroisoquinolines. Chemical Communications (Cambridge, England). 47: 11787-9. PMID 21956547 DOI: 10.1039/C1Cc15050B |
0.472 |
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| 2011 |
Lamani M, Prabhu KR. Iodine-catalyzed amination of benzoxazoles: a metal-free route to 2-aminobenzoxazoles under mild conditions. The Journal of Organic Chemistry. 76: 7938-44. PMID 21866914 DOI: 10.1021/Jo201402A |
0.835 |
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| 2011 |
Gowda MS, Pande SS, Ramakrishna RA, Prabhu KR. Acylation of Grignard reagents mediated by N-methylpyrrolidone: a remarkable selectivity for the synthesis of ketones. Organic & Biomolecular Chemistry. 9: 5365-8. PMID 21706089 DOI: 10.1039/C1Ob05780D |
0.43 |
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| 2011 |
Alagiri K, Prabhu KR. Catalyst-free regio- and stereospecific synthesis of β-sulfonamido dithiocarbamates: efficient ring-opening reactions of N-tosyl aziridines by dialkyldithiocarbamates. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6922-5. PMID 21557366 DOI: 10.1002/Chem.201100817 |
0.443 |
|
| 2011 |
Prabhu K, Maddani M. Metal-Free Deprotection of Terminal Acetonides by Using tert-Butyl Hydroperoxide in Aqueous Medium Synlett. 2011: 821-825. DOI: 10.1055/S-0030-1259917 |
0.833 |
|
| 2011 |
Lamani M, Prabhu KR. Correction to Iodine-Catalyzed Amination of Benzoxazoles: A Metal-Free Route to 2-Aminobenzoxazoles under Mild Conditions The Journal of Organic Chemistry. 76: 9552-9552. DOI: 10.1021/Jo2020455 |
0.788 |
|
| 2011 |
Alagiri K, Prabhu KR. Efficient synthesis of carbonyl compounds: oxidation of azides and alcohols catalyzed by vanadium pentoxide in water using tert-butylhydroperoxide Tetrahedron. 67: 8544-8551. DOI: 10.1016/J.Tet.2011.08.080 |
0.428 |
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| 2011 |
Maddani MR, Prabhu KR. ChemInform Abstract: Metal-Free Deprotection of Terminal Acetonides by Using tert-Butyl Hydroperoxide in Aqueous Medium. Cheminform. 42: no-no. DOI: 10.1002/chin.201130206 |
0.786 |
|
| 2011 |
Maddani MR, Prabhu KR. ChemInform Abstract: Dioxomolybdenum Reagents in Organic Synthesis: Utility of Redox Capability to Design Reduction and Oxidation Cheminform. 42: no-no. DOI: 10.1002/chin.201129215 |
0.803 |
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| 2010 |
Lamani M, Prabhu KR. An efficient oxidation of primary azides catalyzed by copper iodide: a convenient method for the synthesis of nitriles. Angewandte Chemie (International Ed. in English). 49: 6622-5. PMID 20677296 DOI: 10.1002/Anie.201002635 |
0.81 |
|
| 2010 |
Maddani MR, Prabhu KR. A concise synthesis of substituted thiourea derivatives in aqueous medium. The Journal of Organic Chemistry. 75: 2327-32. PMID 20201494 DOI: 10.1021/Jo1001593 |
0.817 |
|
| 2010 |
Maddani MR, Moorthy SK, Prabhu KR. Chemoselective reduction of azides catalyzed by molybdenum xanthate by using phenylsilane as the hydride source Tetrahedron. 66: 329-333. DOI: 10.1016/J.Tet.2009.10.093 |
0.811 |
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| 2010 |
Maddani MR, Moorthy SK, Prabhu KR. ChemInform Abstract: Chemoselective Reduction of Azides Catalyzed by Molybdenum Xanthate by Using Phenylsilane as the Hydride Source. Cheminform. 41. DOI: 10.1002/CHIN.201018066 |
0.802 |
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| 2010 |
Prabhu KR, Kishore PN, Gali H, Katti KV. ChemInform Abstract: De novo Synthetic Design for Air-Stable Bis-Primary Phosphines: Synthetic, Catalytic and Biomedical Motifs Cheminform. 31: no-no. DOI: 10.1002/CHIN.200030281 |
0.526 |
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| 2010 |
ILANKUMARAN P, PRABHU KR, CHANDRASEKARAN S. ChemInform Abstract: Sulfur Transfer Reactions of Tetrathiomolybdate in Water: Synthesis of Alkyl Disulfides from Alkyl Halides. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199808047 |
0.335 |
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| 2010 |
PRABHU KR, CHANDRASEKARAN S. ChemInform Abstract: Highly Chemoselective Synthesis of Functionalized Diselenides from Alkyl Halides Using Benzyltriethylammonium Tetrathiomolybdate. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199741076 |
0.302 |
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| 2008 |
Maddani M, Prabhu KR. Corrigendum to “A chemoselective aerobic oxidation of benzylic azides catalyzed by molybdenum xanthate in an aqueous medium” [Tetrahedron Lett. 49 (2008) 4526] Tetrahedron Letters. 49: 5436. DOI: 10.1016/J.Tetlet.2008.07.001 |
0.814 |
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| 2008 |
Maddani M, Prabhu KR. A chemoselective aerobic oxidation of benzylic azides catalyzed by molybdenum xanthate in an aqueous medium Tetrahedron Letters. 49: 4526-4530. DOI: 10.1016/J.Tetlet.2008.05.047 |
0.83 |
|
| 2008 |
Maddani M, Prabhu KR. ChemInform Abstract: A Chemoselective Aerobic Oxidation of Benzylic Azides Catalyzed by Molybdenum Xanthate in an Aqueous Medium. Cheminform. 39. DOI: 10.1002/CHIN.200842063 |
0.818 |
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| 2008 |
Maddani M, Prabhu KR. ChemInform Abstract: A Convenient Method for the Synthesis of Substituted Thioureas. Cheminform. 39. DOI: 10.1002/CHIN.200801054 |
0.806 |
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| 2007 |
Maddani M, Prabhu KR. A convenient method for the synthesis of substituted thioureas Tetrahedron Letters. 48: 7151-7154. DOI: 10.1016/J.Tetlet.2007.07.212 |
0.835 |
|
| 2007 |
Arulraj J, Rajamathi JT, Prabhu KR, Rajamathi M. Anionic clays as hosts for anchored synthesis: Interlayer bromination of maleate and fumarate ions in nickel–zinc layered hydroxy double salt Solid State Sciences. 9: 812-816. DOI: 10.1016/J.Solidstatesciences.2007.06.007 |
0.329 |
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| 2005 |
Sridhar PR, Prabhu KR, Chandrasekaran S. Synthesis of Thioglycosides by Tetrathiomolybdate-Mediated Michael Additions of Masked Thiolates. Cheminform. 36. DOI: 10.1002/CHIN.200514195 |
0.712 |
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| 2004 |
Raghuraman K, Pillarsetty N, Prabhu KR, Katti KK, Katti KV. Unprecedented rhodium-mediated catalytic transfer hydrogenation of a phosphonate functionalized olefin in ecofriendly media Inorganica Chimica Acta. 357: 2933-2938. DOI: 10.1016/J.Ica.2004.01.005 |
0.739 |
|
| 2004 |
Sridhar P, Prabhu K, Chandrasekaran S. Synthesis of Thioglycosides by Tetrathiomolybdate-Mediated Michael Additions of Masked Thiolates European Journal of Organic Chemistry. 2004: 4809-4815. DOI: 10.1002/Ejoc.200400360 |
0.844 |
|
| 2003 |
Sridhar PR, Prabhu KR, Chandrasekaran S. Selective reduction of anomeric azides to amines with tetrathiomolybdate: synthesis of beta-D-glycosylamines. The Journal of Organic Chemistry. 68: 5261-4. PMID 12816487 DOI: 10.1021/Jo0266947 |
0.8 |
|
| 2003 |
Devan N, Sureshkumar D, Beadham I, Prabhu KR, Chandrasekaran S. Michael Addition of Masked Thiolates to Conjugated Systems in Aqueous Media Promoted by Ammonium Tetrathiomolybdate. Cheminform. 34. DOI: 10.1002/CHIN.200309027 |
0.754 |
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| 2002 |
Devan N, Sridhar PR, Prabhu KR, Chandrasekaran S. Tetrathiomolybdate assisted epoxide ring opening with masked thiolates and selenoates: multistep reactions in one pot. The Journal of Organic Chemistry. 67: 9417-20. PMID 12492347 DOI: 10.1021/Jo0263418 |
0.799 |
|
| 2002 |
Kothari KK, Gali H, Prabhu KR, Pillarsetty N, Owen NK, Katti KV, Hoffman TJ, Volkert WA. Synthesis and characterization of (99m)Tc- and (188)Re-complexes with a diamido-dihydroxymethylenephosphine-based bifunctional chelating agent (N(2)P(2)-BFCA). Nuclear Medicine and Biology. 29: 83-9. PMID 11786279 DOI: 10.1016/S0969-8051(01)00280-3 |
0.695 |
|
| 2002 |
Kannan R, Pillarsetty N, Prabhu KR, Katti KV. Novel Green Chemistry in the Phosphonate Assisted Catalytic Hydrogenation of Olefins Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1951-1951. DOI: 10.1080/10426500213380 |
0.734 |
|
| 2002 |
Chandrasekaran S, Prabhu KR, Devan N. Chemistry of Tetrathiomolybdate: Applications in Organic Synthesis Synlett. 2002: 1762-1778. DOI: 10.1055/S-2002-34863 |
0.738 |
|
| 2001 |
Ilankumaran P, Prabhu KR, Chandrasekaran S. ChemInform Abstract: Reaction of β-Haloenones with Tetrathiomolybdate: Synthesis of Vinyl Disulfides. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200117054 |
0.695 |
|
| 2000 |
Prabhu KR, Sivanand PS, Chandrasekaran S. A Tandem Sulfur Transfer/Reduction/Michael Addition Mediated by Benzyltriethylammonium Tetrathiomolybdate. Angewandte Chemie (International Ed. in English). 39: 4316-4319. PMID 29711888 DOI: 10.1002/1521-3773(20001201)39:23<4316::Aid-Anie4316>3.0.Co;2-E |
0.675 |
|
| 2000 |
Gali H, Prabhu KR, Karra SR, Katti KV. Facile Ring-Opening Reactions of Phthalimides as a New Strategy to Synthesize Amide-Functionalized Phosphonates, Primary Phosphines, and Bisphosphines The Journal of Organic Chemistry. 65: 676-680. DOI: 10.1021/Jo991067B |
0.665 |
|
| 2000 |
Prabhu KR, Pillarsetty N, Gali H, Katti KV. Unprecedented Selective Aminolysis: Aminopropyl Phosphine as a Building Block for a New Family of Air Stable Mono-, Bis-, and Tris-Primary Phosphines Journal of the American Chemical Society. 122: 1554-1555. DOI: 10.1021/Ja993504+ |
0.754 |
|
| 1999 |
Ramesha AR, Bhat S, Prabhu KR. ISOMERIZATION OF LONGIFOLENE TO ISOLONGIFOLENE CATALYZED BY MONTMORILLONITE CLAY Organic Preparations and Procedures International. 31: 227-230. DOI: 10.1080/00304949909355720 |
0.309 |
|
| 1998 |
Prabhu KR, Sivanand PS, Chandrsekaran S. A New Methodology for the Reductive Cyclization of ω-Azido Carbonyl Compounds Mediated by Tetrathiomolybdate: Application to an Efficient Synthesis of Pyrrolo[2,1-c][1,4]benzodiazepines Synlett. 1998: 47-48. DOI: 10.1055/S-1998-1057884 |
0.422 |
|
| 1997 |
Ilankumaran P, Prabhu KR, Chandrasekaran S. Sulfur Transfer Reactions of Tetrathiomolybdate in Water: Synthesis of Alkyl Disulfides from Alkyl Halides Synthetic Communications. 27: 4031-4034. DOI: 10.1080/00397919708005447 |
0.729 |
|
| 1997 |
Prabhu KR, Chandrasekaran S. Highly chemoselective synthesis of functionalized diselenides from alkyl halides using benzyltriethylammonium tetrathiomolybdate Chemical Communications. 1021-1022. DOI: 10.1039/A701512G |
0.724 |
|
| 1995 |
Prabhu KR, Ramesha AR, Chandrasekaran S. Reductive dimerization of organic thiocyanates to disulfides mediated by tetrathiomolybdate The Journal of Organic Chemistry. 60: 7142-7143. DOI: 10.1021/Jo00127A017 |
0.643 |
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