Year |
Citation |
Score |
2025 |
Mondal A, Phukan HJ, Mohar K, Pal D, Sharma R, Purkayastha S, Guha AK, Srimani D. Designing a NNO-manganese complex overcoming steric constraints in (de)hydrogenative coupling. Chemical Communications (Cambridge, England). PMID 40034079 DOI: 10.1039/d5cc00048c |
0.767 |
|
2024 |
Roy M, Mallick I, Mahapatra M, Srimani D. Substituent-Dependent, Switchable Synthesis of Nonaromatic and Aromatic Heterocyclic Sulfones Using Visible Light. Organic Letters. PMID 39441842 DOI: 10.1021/acs.orglett.4c03587 |
0.787 |
|
2024 |
Pal D, Sarmah R, Mondal A, Mallick I, Srimani D. Well-defined cobalt(II)-catalyzed synthesis of perimidine derivatives acceptorless dehydrogenative annulation. Organic & Biomolecular Chemistry. PMID 39378099 DOI: 10.1039/d4ob01306a |
0.725 |
|
2024 |
Samanta A, Chaubey A, Pal D, Majhi K, Srimani D. Redox-enabled cooperative catalysis by activating secondary alcohols using low-valent Zn complexes. Chemical Communications (Cambridge, England). PMID 39224069 DOI: 10.1039/d4cc03407d |
0.833 |
|
2024 |
Roy M, Sardar B, Mallick I, Srimani D. Generation of alkyl and acyl radicals by visible-light photoredox catalysis: direct activation of C-O bonds in organic transformations. Beilstein Journal of Organic Chemistry. 20: 1348-1375. PMID 38887583 DOI: 10.3762/bjoc.20.119 |
0.797 |
|
2024 |
Samanta A, Behera P, Chaubey A, Mondal A, Pal D, Mohar K, Roy L, Srimani D. Experimental and theoretical insights for designing Zn complexes to trigger chemo-selective hetero-coupling of alcohols. Chemical Communications (Cambridge, England). PMID 38505958 DOI: 10.1039/d4cc00864b |
0.82 |
|
2024 |
Pal D, Mondal A, Sarmah R, Srimani D. Designing Cobalt(II) Complexes for Tandem Dehydrogenative Synthesis of Quinoline and Quinazoline Derivatives. Organic Letters. PMID 38194364 DOI: 10.1021/acs.orglett.3c03944 |
0.702 |
|
2023 |
Mondal A, Pal D, Phukan HJ, Roy M, Kumar S, Purkayastha S, Guha AK, Srimani D. Manganese Complex Catalyzed Sequential Multi-component Reaction: Enroute to a Quinoline-Derived Azafluorenes. Chemsuschem. e202301138. PMID 38096176 DOI: 10.1002/cssc.202301138 |
0.822 |
|
2023 |
Mondal A, Phukan HJ, Pal D, Kumar S, Roy M, Srimani D. Well-defined Mn(II)-complex Catalyzed Switchable De(hydrogenative) Csp3-H Functionalization of Methyl Heteroarenes: A Sustainable Approach for Diversification of Heterocyclic Motifs. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303315. PMID 37933814 DOI: 10.1002/chem.202303315 |
0.818 |
|
2023 |
Sardar B, Pal D, Sarmah R, Srimani D. Ruthenium-catalyzed dehydrogenative cyclization to synthesize polysubstituted 4-quinolones under solvent-free conditions. Chemical Communications (Cambridge, England). PMID 37431578 DOI: 10.1039/d3cc02426a |
0.831 |
|
2022 |
Roy M, Jamatia R, Samanta A, Mohar K, Srimani D. Change in the Product Selectivity in the Visible Light-Induced Selenium Radical-Mediated 1,4-Aryl Migration Process. Organic Letters. 24: 8180-8185. PMID 36305909 DOI: 10.1021/acs.orglett.2c03260 |
0.727 |
|
2022 |
Sharma R, Samanta A, Sardar B, Roy M, Srimani D. Progressive study on ruthenium catalysis for de(hydrogenative) alkylation and alkenylation using alcohols as a sustainable source. Organic & Biomolecular Chemistry. PMID 36200985 DOI: 10.1039/d2ob01323a |
0.803 |
|
2022 |
Sardar B, Jamatia R, Samanta A, Srimani D. Ru Doped Hydrotalcite Catalyzed Borrowing Hydrogen-Mediated N-Alkylation of Benzamides, Sulfonamides, and Dehydrogenative Synthesis of Quinazolinones. The Journal of Organic Chemistry. PMID 35442678 DOI: 10.1021/acs.joc.1c02913 |
0.822 |
|
2022 |
Mondal A, Sharma R, Dutta B, Pal D, Srimani D. Well-Defined NNS-Mn Complex Catalyzed Selective Synthesis of C-3 Alkylated Indoles and Bisindolylmethanes Using Alcohols. The Journal of Organic Chemistry. 87: 3989-4000. PMID 35258302 DOI: 10.1021/acs.joc.1c02702 |
0.766 |
|
2021 |
Mondal A, Sharma R, Pal D, Srimani D. Manganese catalyzed switchable -alkylation/alkenylation of fluorenes and indene with alcohols. Chemical Communications (Cambridge, England). PMID 34541595 DOI: 10.1039/d1cc03529k |
0.758 |
|
2021 |
Biswas N, Srimani D. Ru-Catalyzed Selective Catalytic Methylation and Methylenation Reaction Employing Methanol as the C1 Source. The Journal of Organic Chemistry. PMID 34263597 DOI: 10.1021/acs.joc.1c01185 |
0.788 |
|
2021 |
Biswas N, Srimani D. Synthesis of 1,8-Dioxo-decahydroacridine Derivatives Ru-Catalyzed Acceptorless Dehydrogenative Multicomponent Reaction. The Journal of Organic Chemistry. PMID 34170141 DOI: 10.1021/acs.joc.1c01075 |
0.785 |
|
2020 |
Daw P, Kumar A, Oren D, Espinosa-Jalapa NA, Srimani D, Diskin-Posner Y, Leitus G, Shimon LJW, Carmieli R, Ben-David Y, Milstein D. Redox Noninnocent Nature of Acridine-Based Pincer Complexes of 3d Metals and C–C Bond Formation Organometallics. 39: 279-285. DOI: 10.1021/Acs.Organomet.9B00607 |
0.774 |
|
2020 |
Biswas N, Sharma R, Srimani D. Ruthenium Pincer Complex Catalyzed Selective Synthesis of C‐3 Alkylated Indoles and Bisindolylmethanes Directly from Indoles and Alcohols Advanced Synthesis & Catalysis. 362: 2902-2910. DOI: 10.1002/Adsc.202000326 |
0.836 |
|
2019 |
Das K, Mondal A, Pal D, Srimani D. Sustainable Synthesis of Quinazoline and 2-Aminoquinoline via Dehydrogenative Coupling of 2-Aminobenzyl Alcohol and Nitrile Catalyzed by Phosphine-Free Manganese Pincer Complex. Organic Letters. PMID 31008616 DOI: 10.1021/Acs.Orglett.9B00939 |
0.838 |
|
2019 |
Biswas N, Das K, Sardar B, Srimani D. Acceptorless dehydrogenative construction of C[double bond, length as m-dash]N and C[double bond, length as m-dash]C bonds through catalytic aza-Wittig and Wittig reactions in the presence of an air-stable ruthenium pincer complex. Dalton Transactions (Cambridge, England : 2003). PMID 30994638 DOI: 10.1039/C8Dt04725A |
0.802 |
|
2019 |
Das K, Mondal A, Pal D, Srivastava HK, Srimani D. Phosphine-Free Well-Defined Mn(I) Complex-Catalyzed Synthesis of Amine, Imine, and 2,3-Dihydro-1H-perimidine via Hydrogen Autotransfer or Acceptorless Dehydrogenative Coupling of Amine and Alcohol Organometallics. 38: 1815-1825. DOI: 10.1021/Acs.Organomet.9B00131 |
0.811 |
|
2018 |
Das K, Mondal A, Srimani D. Phosphine free Mn-complex catalysed dehydrogenative C-C and C-heteroatom bond formation: a sustainable approach to synthesize quinoxaline, pyrazine, benzothiazole and quinoline derivatives. Chemical Communications (Cambridge, England). PMID 30167623 DOI: 10.1039/C8Cc05877F |
0.787 |
|
2018 |
DAS K, Mondal A, Srimani D. Selective Synthesis of 2-substituted and 1,2-disubstituted Benzimidazoles Directly from Aromatic Diamines and Alcohols Catalyzed by Molecularly Defined Non-Phosphine Manganese (I) Complex. The Journal of Organic Chemistry. PMID 29993244 DOI: 10.1021/Acs.Joc.8B01316 |
0.798 |
|
2017 |
Mukherjee A, Srimani D, Ben-David Y, Milstein D. Low-Pressure Hydrogenation of Nitriles to Primary Amines Catalyzed by Ruthenium Pincer Complexes. Scope and mechanism Chemcatchem. 9: 559-563. DOI: 10.1002/Cctc.201601416 |
0.715 |
|
2015 |
Mukherjee A, Srimani D, Chakraborty S, Ben-David Y, Milstein D. Selective Hydrogenation of Nitriles to Primary Amines Catalyzed by a Cobalt Pincer Complex. Journal of the American Chemical Society. PMID 26131688 DOI: 10.1021/Jacs.5B04879 |
0.802 |
|
2015 |
Srimani D, Mukherjee A, Goldberg AF, Leitus G, Diskin-Posner Y, Shimon LJ, Ben David Y, Milstein D. Cobalt-Catalyzed Hydrogenation of Esters to Alcohols: Unexpected Reactivity Trend Indicates Ester Enolate Intermediacy. Angewandte Chemie (International Ed. in English). PMID 25914240 DOI: 10.1002/Anie.201502418 |
0.815 |
|
2014 |
Srimani D, Leitus G, Ben-David Y, Milstein D. Direct catalytic olefination of alcohols with sulfones. Angewandte Chemie (International Ed. in English). 53: 11092-5. PMID 25163718 DOI: 10.1002/Anie.201407281 |
0.691 |
|
2014 |
Balaraman E, Srimani D, Diskin-Posner Y, Milstein D. Direct Synthesis of Secondary Amines From Alcohols and Ammonia Catalyzed by a Ruthenium Pincer Complex Catalysis Letters. 145: 139-144. DOI: 10.1007/S10562-014-1422-2 |
0.801 |
|
2014 |
Srimani D, Balaraman E, Hu P, Ben-David Y, Milstein D. ChemInform Abstract: Formation of Tertiary Amides and Dihydrogen by Dehydrogenative Coupling of Primary Alcohols with Secondary Amines Catalyzed by Ruthenium Bipyridine-Based Pincer Complexes. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201415054 |
0.728 |
|
2014 |
Srimani D, Leitus G, Ben-David Y, Milstein D. Direct catalytic olefination of alcohols with sulfones Angewandte Chemie - International Edition. 53: 11092-11095. DOI: 10.1002/anie.201407281 |
0.591 |
|
2013 |
Srimani D, Diskin-Posner Y, Ben-David Y, Milstein D. Iron pincer complex catalyzed, environmentally benign, E-selective semi-hydrogenation of alkynes. Angewandte Chemie (International Ed. in English). 52: 14131-4. PMID 24353233 DOI: 10.1002/Anie.201306629 |
0.515 |
|
2013 |
Srimani D, Ben-David Y, Milstein D. Direct synthesis of pyridines and quinolines by coupling of γ-amino-alcohols with secondary alcohols liberating H2 catalyzed by ruthenium pincer complexes. Chemical Communications (Cambridge, England). 49: 6632-4. PMID 23771175 DOI: 10.1039/C3Cc43227K |
0.703 |
|
2013 |
Srimani D, Ben-David Y, Milstein D. Direct synthesis of pyrroles by dehydrogenative coupling of β-aminoalcohols with secondary alcohols catalyzed by ruthenium pincer complexes. Angewandte Chemie (International Ed. in English). 52: 4012-5. PMID 23468418 DOI: 10.1002/Anie.201300574 |
0.661 |
|
2013 |
Srimani D, Balaraman E, Gnanaprasam B, Ben-David Y, Milstein D. ChemInform Abstract: Ruthenium Pincer-Catalyzed Cross-Dehydrogenative Coupling of Primary Alcohols with Secondary Alcohols under Neutral Conditions. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201309055 |
0.697 |
|
2013 |
Srimani D, Balaraman E, Hu P, Ben-David Y, Milstein D. Formation of tertiary amides and dihydrogen by dehydrogenative coupling of primary alcohols with secondary amines catalyzed by ruthenium bipyridine-based pincer complexes Advanced Synthesis and Catalysis. 355: 2525-2530. DOI: 10.1002/Adsc.201300620 |
0.785 |
|
2012 |
Srimani D, Feller M, Ben-David Y, Milstein D. Catalytic coupling of nitriles with amines to selectively form imines under mild hydrogen pressure. Chemical Communications (Cambridge, England). 48: 11853-5. PMID 23125982 DOI: 10.1039/C2Cc36639H |
0.596 |
|
2012 |
Bej A, Srimani D, Sarkar A. Palladium nanoparticle catalysis: borylation of aryl and benzyl halides and one-pot biaryl synthesis via sequential borylation-Suzuki–Miyaura coupling Green Chemistry. 14: 661. DOI: 10.1039/C2Gc16111G |
0.679 |
|
2012 |
Bej A, Srimani D, Sarkar A. ChemInform Abstract: Palladium Nanoparticle Catalysis: Borylation of Aryl and Benzyl Halides and One-Pot Biaryl Synthesis via Sequential Borylation-Suzuki-Miyaura Coupling. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201231088 |
0.59 |
|
2012 |
Srimani D, Balaraman E, Gnanaprakasam B, Ben-David Y, Milstein D. Ruthenium pincer-catalyzed cross-dehydrogenative coupling of primary alcohols with secondary alcohols under neutral conditions Advanced Synthesis and Catalysis. 354: 2403-2406. DOI: 10.1002/Adsc.201200438 |
0.778 |
|
2010 |
Dhara K, Sarkar K, Srimani D, Saha SK, Chattopadhyay P, Bhaumik A. A new functionalized mesoporous matrix supported Pd(II)-Schiff base complex: an efficient catalyst for the Suzuki-Miyaura coupling reaction. Dalton Transactions (Cambridge, England : 2003). 39: 6395-402. PMID 20532296 DOI: 10.1039/C003142A |
0.423 |
|
2010 |
Srimani D, Bej A, Sarkar A. Palladium nanoparticle catalyzed Hiyama coupling reaction of benzyl halides. The Journal of Organic Chemistry. 75: 4296-9. PMID 20491503 DOI: 10.1021/Jo1003373 |
0.638 |
|
2009 |
Sawoo S, Srimani D, Dutta P, Lahiri R, Sarkar A. Size controlled synthesis of Pd nanoparticles in water and their catalytic application in C–C coupling reactions Tetrahedron. 65: 4367-4374. DOI: 10.1016/J.Tet.2009.03.062 |
0.775 |
|
2009 |
Sawoo S, Srimani D, Dutta P, Lahiri R, Sarkar A. ChemInform Abstract: Size Controlled Synthesis of Pd Nanoparticles in Water and Their Catalytic Application in C-C Coupling Reactions. Cheminform. 40. DOI: 10.1002/chin.200938089 |
0.789 |
|
2009 |
Srimani D, Sarkar A. ChemInform Abstract: Benzaldimines as Ligands for Palladium in Suzuki-Miyaura Reactions. Cheminform. 40. DOI: 10.1002/CHIN.200907045 |
0.594 |
|
2008 |
Srimani D, Sarkar A. Benzaldimines as ligands for palladium in Suzuki–Miyaura reactions Tetrahedron Letters. 49: 6304-6307. DOI: 10.1016/J.Tetlet.2008.08.056 |
0.655 |
|
2007 |
Srimani D, Sawoo S, Sarkar A. Convenient synthesis of palladium nanoparticles and catalysis of Hiyama coupling reaction in water. Organic Letters. 9: 3639-42. PMID 17676861 DOI: 10.1021/Ol7015143 |
0.803 |
|
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