| Year |
Citation |
Score |
| 2023 |
Mishra S, Patil NT. Gold-catalyzed alkenylation and arylation of phosphorothioates. Chemical Science. 14: 13134-13139. PMID 38023501 DOI: 10.1039/d3sc04888h |
0.43 |
|
| 2023 |
Bhoyare VW, Tathe AG, Gandon V, Patil NT. Unlocking the Chain-Walking Process in Gold Catalysis. Angewandte Chemie (International Ed. in English). 62: e202312786. PMID 37779346 DOI: 10.1002/anie.202312786 |
0.824 |
|
| 2023 |
Sancheti SP, Singh Y, Mane MV, Patil NT. Gold-Catalyzed 1,2-Dicarbofunctionalization of Alkynes with Organohalides. Angewandte Chemie (International Ed. in English). 62: e202310493. PMID 37649285 DOI: 10.1002/anie.202310493 |
0.826 |
|
| 2023 |
Kumar A, Shukla K, Ahsan S, Paul A, Patil NT. Electrochemical Gold-Catalyzed 1,2-Difunctionalization of C-C Multiple Bonds. Angewandte Chemie (International Ed. in English). e202308636. PMID 37491811 DOI: 10.1002/anie.202308636 |
0.44 |
|
| 2023 |
Ambegave SB, More TR, Patil NT. Gold-based enantioselective bimetallic catalysis. Chemical Communications (Cambridge, England). 59: 8007-8016. PMID 37285287 DOI: 10.1039/d3cc01966g |
0.81 |
|
| 2023 |
Bhoyare VW, Sosa Carrizo ED, Chintawar CC, Gandon V, Patil NT. Gold-Catalyzed Heck Reaction. Journal of the American Chemical Society. 145: 8810-8816. PMID 37061943 DOI: 10.1021/jacs.3c02544 |
0.829 |
|
| 2023 |
Kumar A, Das A, Patil NT. Gold-Catalyzed Aryl-Alkenylation of Alkenes. Organic Letters. PMID 37058129 DOI: 10.1021/acs.orglett.3c01044 |
0.532 |
|
| 2022 |
Mule RD, Kumar A, Sancheti SP, Senthilkumar B, Kumar H, Patil NT. BQ-AurIPr: a redox-active anticancer Au(i) complex that induces immunogenic cell death. Chemical Science. 13: 10779-10785. PMID 36320699 DOI: 10.1039/d2sc03756d |
0.725 |
|
| 2022 |
Koner AL, Chopra D, Patil NT. AIEgens Based on Anion-π+ Interactions: Design, Synthesis, Photophysical Properties, and their Applications in Material Science and Biology. Chembiochem : a European Journal of Chemical Biology. PMID 35945807 DOI: 10.1002/cbic.202200320 |
0.621 |
|
| 2022 |
Tathe AG, Patil NT. Ligand-Enabled Gold-Catalyzed C(sp)-S Cross-Coupling Reactions. Organic Letters. PMID 35696657 DOI: 10.1021/acs.orglett.2c01692 |
0.837 |
|
| 2022 |
Chintawar CC, Bhoyare VW, Mane MV, Patil NT. Enantioselective Au(I)/Au(III) Redox Catalysis Enabled by Chiral (P,N)-Ligands. Journal of the American Chemical Society. PMID 35436097 DOI: 10.1021/jacs.2c02799 |
0.808 |
|
| 2022 |
Mule RD, Roy R, Mandal K, Chopra D, Dutta T, Sancheti SP, Shinde PS, Banerjee S, Koner AL, Bhowal R, Senthilkumar B, Patil NT. Interplay of Anion-π+ and π+-π+ Interactions ….. Applications in Live Cell Mitochondrial Imaging. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35429368 DOI: 10.1002/chem.202200632 |
0.769 |
|
| 2022 |
Patil NT, Das A. Enantioselective C-H Functionalization Reactions under Gold Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35014732 DOI: 10.1002/chem.202104371 |
0.787 |
|
| 2021 |
Yorimitsu H, Kotora M, Patil NT. Special Issue: Recent Advances in Transition-Metal Catalysis. Chemical Record (New York, N.Y.). 21: 3335-3337. PMID 34904783 DOI: 10.1002/tcr.202100305 |
0.265 |
|
| 2021 |
Paroi B, Sancheti SP, Patil NT. 1,2-Aminofunctionalization Reactions of Pyridino-Alkynes via Carbophilic Activation. Chemical Record (New York, N.Y.). PMID 34669247 DOI: 10.1002/tcr.202100145 |
0.821 |
|
| 2021 |
Bhoyare VW, Tathe AG, Das A, Chintawar CC, Patil NT. The interplay of carbophilic activation and Au(I)/Au(III) catalysis: an emerging technique for 1,2-difunctionalization of C-C multiple bonds. Chemical Society Reviews. PMID 34323240 DOI: 10.1039/d0cs00700e |
0.806 |
|
| 2021 |
Chintawar CC, Yadav AK, Kumar A, Sancheti SP, Patil NT. Divergent Gold Catalysis: Unlocking Molecular Diversity through Catalyst Control. Chemical Reviews. PMID 33555193 DOI: 10.1021/acs.chemrev.0c00903 |
0.818 |
|
| 2020 |
Tathe AG, Chintawar CC, Bhoyare VW, Patil NT. Ligand-enabled gold-catalyzed 1,2-heteroarylation of alkenes. Chemical Communications (Cambridge, England). PMID 32666971 DOI: 10.1039/d0cc03707a |
0.809 |
|
| 2020 |
Banerjee S, Ambegave SB, Mule RD, Senthilkumar B, Patil NT. Gold-Catalyzed Alkynylative Meyer-Schuster Rearrangement. Organic Letters. PMID 32510962 DOI: 10.1021/Acs.Orglett.0C01596 |
0.789 |
|
| 2020 |
Patil NT, Chintawar CC, Yadav AK. Gold-Catalyzed 1,2-Diarylation of Alkenes. Angewandte Chemie (International Ed. in English). PMID 32203638 DOI: 10.1002/Anie.202002141 |
0.829 |
|
| 2020 |
Banerjee S, Bhoyare VW, Patil NT. Gold and hypervalent iodine(iii): liaisons over a decade for electrophilic functional group transfer reactions. Chemical Communications (Cambridge, England). PMID 32090230 DOI: 10.1039/D0Cc00106F |
0.829 |
|
| 2019 |
Patil NT, Sancheti SP, Akram MO, Roy R, Bedi V, Kundu S. ortho -Oxygenative 1,2-Difunctionalization of Diarylalkynes under Merged Gold/Organophotoredox Relay Catalysis. Chemistry, An Asian Journal. PMID 31589800 DOI: 10.1002/Asia.201901275 |
0.828 |
|
| 2019 |
Akram MO, Das A, Chakrabarty I, Patil NT. Ligand-Enabled Gold-Catalyzed C(sp)-N Cross-Coupling Reactions of Aryl Iodides with Amines. Organic Letters. PMID 31556300 DOI: 10.1021/Acs.Orglett.9B03082 |
0.837 |
|
| 2019 |
Chintawar CC, Mane MV, Tathe AG, Biswas S, Patil NT. Gold-Catalyzed Cycloisomerization of Pyridine-Bridged 1,8-Diynes: An Expedient Access to Luminescent Cycl[3.2.2]azines. Organic Letters. PMID 31453703 DOI: 10.1021/Acs.Orglett.9B02677 |
0.81 |
|
| 2019 |
Shaikh AC, Banerjee S, Mule RD, Bera S, Patil NT. External Oxidant-Dependent Reactivity Switch in Copper-Mediated Intramolecular Carboamination of Alkynes: Access to a New Class of Fluorescent Ionic Nitrogen-Doped Polycyclic Aromatic Hydrocarbons. The Journal of Organic Chemistry. PMID 30813732 DOI: 10.1021/Acs.Joc.9B00120 |
0.787 |
|
| 2019 |
Shaikh AC, Verma ME, Mule RD, Banerjee S, Kulkarni PP, Patil NT. Ionic Pyridinium-Oxazole Dyads: Design, Synthesis, and their Application in Mitochondrial Imaging. The Journal of Organic Chemistry. PMID 30638382 DOI: 10.1021/Acs.Joc.8B02528 |
0.786 |
|
| 2018 |
Bagle PN, Mane MV, Sancheti SP, Gade AB, Shaikh SR, Baik MH, Patil NT. Gold(I)-Catalyzed Hydroxy Group Assisted C(sp)-H Alkylation of Enaminones with Diazo Compounds To Access 3-Alkyl Chromones. Organic Letters. PMID 30586309 DOI: 10.1021/Acs.Orglett.8B03989 |
0.791 |
|
| 2018 |
Banerjee S, Senthilkumar B, Patil NT. Gold-Catalyzed 1,2-Oxyalkynylation of N-Allenamides with Ethylnylbenziodoxolones. Organic Letters. PMID 30548074 DOI: 10.1021/Acs.Orglett.8B03651 |
0.693 |
|
| 2018 |
Mule RD, Shaikh AC, Gade AB, Patil NT. A new class of N-doped ionic PAHs via intramolecular [4+2]-cycloaddition between arylpyridines and alkynes. Chemical Communications (Cambridge, England). PMID 30283940 DOI: 10.1039/C8Cc05743E |
0.8 |
|
| 2018 |
Akram MO, Banerjee S, Saswade SS, Bedi V, Patil NT. Oxidant-free oxidative gold catalysis: the new paradigm in cross-coupling reactions. Chemical Communications (Cambridge, England). PMID 30168538 DOI: 10.1039/C8Cc05601C |
0.84 |
|
| 2018 |
Chakrabarty I, Akram MO, Biswas S, Patil NT. Visible light mediated desilylative C(sp)-C(sp) cross-coupling reactions of arylsilanes with aryldiazonium salts under Au(i)/Au(iii) catalysis. Chemical Communications (Cambridge, England). PMID 29900463 DOI: 10.1039/C8Cc03925A |
0.815 |
|
| 2018 |
Akram MO, Shinde PS, Chintawar CC, Patil NT. Gold(i)-catalyzed cross-coupling reactions of aryldiazonium salts with organostannanes. Organic & Biomolecular Chemistry. PMID 29632948 DOI: 10.1039/C8Ob00630J |
0.819 |
|
| 2018 |
Gade AB, Bagle PN, Shinde PS, Bhardwaj V, Banerjee S, Chande A, Patil NT. Catalytic Enantioselective 1,3-Alkyl Shift in Alkyl Aryl Ethers: Efficient Synthesis of Optically Active 3,3'-Diaryloxindoles. Angewandte Chemie (International Ed. in English). PMID 29573526 DOI: 10.1002/Anie.201801650 |
0.808 |
|
| 2017 |
Ramesh C, Nayak BS, Pai VB, Patil NT, George A, George LS, Devi ES. Effect of Preoperative Education on Postoperative Outcomes Among Patients Undergoing Cardiac Surgery: A Systematic Review and Meta-Analysis. Journal of Perianesthesia Nursing : Official Journal of the American Society of Perianesthesia Nurses. 32: 518-529.e2. PMID 29157759 DOI: 10.1016/j.jopan.2016.11.011 |
0.184 |
|
| 2017 |
Chandrababu R, Nayak BS, Pai VB, Patil NT, George A, George LS, Devi ES. Effect of Complementary Therapies in Patients Following Cardiac Surgery: A Narrative Review. Holistic Nursing Practice. 31: 315-324. PMID 28786889 DOI: 10.1097/HNP.0000000000000226 |
0.204 |
|
| 2017 |
Bansode AH, Shaikh SR, Gonnade RG, Patil NT. Intramolecular ipso-arylative cyclization of aryl-alkynoates and N-arylpropiolamides with aryldiazonium salts through merged gold/visible light photoredox catalysis. Chemical Communications (Cambridge, England). PMID 28752169 DOI: 10.1039/C7Cc04010E |
0.827 |
|
| 2017 |
Banerjee S, Patil NT. Exploiting the dual role of ethynylbenziodoxolones in gold-catalyzed C(sp)-C(sp) cross-coupling reactions. Chemical Communications (Cambridge, England). PMID 28657099 DOI: 10.1039/C7Cc04283C |
0.716 |
|
| 2017 |
Akram MO, Mali PS, Patil NT. Cross-Coupling Reactions of Aryldiazonium Salts with Allylsilanes under Merged Gold/Visible-Light Photoredox Catalysis. Organic Letters. PMID 28590758 DOI: 10.1021/Acs.Orglett.7B01148 |
0.834 |
|
| 2017 |
Shinde PS, Patil NT. Gold-Catalyzed Dehydrazinative C(sp)-S Coupling Reactions of Arylsulfonyl Hydrazides with Ethynylbenziodoxolones for Accessing Alkynyl Sulfones European Journal of Organic Chemistry. 2017: 3512-3515. DOI: 10.1002/Ejoc.201700524 |
0.849 |
|
| 2016 |
Inamdar SM, Gonnade RG, Patil NT. Synthesis of annulated bis-indoles through Au(i)/Brønsted acid-catalyzed reactions of (1H-indol-3-yl)(aryl)methanols with 2-(arylethynyl)-1H-indoles. Organic & Biomolecular Chemistry. PMID 28009921 DOI: 10.1039/C6Ob02595A |
0.544 |
|
| 2016 |
Shaikh AC, Ranade DS, Rajamohanan PR, Kulkarni PP, Patil NT. Oxidative Intramolecular 1,2-Amino-Oxygenation of Alkynes under Au(I) /Au(III) -Catalysis: Discovery of Pyridinium-Oxazole Dyad as an Ionic Fluorophore. Angewandte Chemie (International Ed. in English). PMID 28000332 DOI: 10.1002/Anie.201609335 |
0.79 |
|
| 2016 |
Chakrabarty I, Inamdar SM, Akram MO, Gade AB, Banerjee S, Bera S, Patil NT. [3+2]-Annulation of platinum-bound azomethine ylides with distal C[double bond, length as m-dash]C bonds of N-allenamides. Chemical Communications (Cambridge, England). PMID 27917422 DOI: 10.1039/C6Cc07874E |
0.795 |
|
| 2016 |
Bagle PN, Mane MV, Vanka K, Shinde DR, Shaikh SR, Gonnade RG, Patil NT. Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides. Chemical Communications (Cambridge, England). PMID 27901528 DOI: 10.1039/C6Cc08385D |
0.794 |
|
| 2016 |
Akram MO, Bera S, Patil NT. A facile strategy for accessing 3-alkynylchromones through gold-catalyzed alkynylation/cyclization of o-hydroxyarylenaminones. Chemical Communications (Cambridge, England). 52: 12306-12309. PMID 27711496 DOI: 10.1039/C6Cc07119H |
0.8 |
|
| 2016 |
Shinde PS, Shaikh AC, Patil NT. Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes. Chemical Communications (Cambridge, England). PMID 27276437 DOI: 10.1039/C6Cc03414D |
0.841 |
|
| 2016 |
Gade AB, Patil NT. Gold(I)-Catalyzed Hydroaminaloxylation and Petasis-Ferrier Rearrangement Cascade of Aminaloalkynes. Organic Letters. PMID 27028540 DOI: 10.1021/Acs.Orglett.6B00585 |
0.68 |
|
| 2016 |
Shaikh AC, Shinde DR, Patil NT. Gold vs Rhodium Catalysis: Tuning Reactivity through Catalyst Control in the C-H Alkynylation of Isoquinolones. Organic Letters. PMID 26886569 DOI: 10.1021/Acs.Orglett.6B00175 |
0.764 |
|
| 2016 |
Inamdar SM, Chakrabarty I, Patil NT. A unified approach to pyrrole-embedded aza-heterocyclic scaffolds based on the RCM/isomerization/cyclization cascade catalyzed by a Ru/B-H binary catalyst system Rsc Advances. 6: 34428-34433. DOI: 10.1039/C6Ra05646F |
0.809 |
|
| 2016 |
Inamdar SM, Chakrabarty I, Patil NT. ChemInform Abstract: A Unified Approach to Pyrrole-Embedded Aza-Heterocyclic Scaffolds Based on the RCM/Isomerization/Cyclization Cascade Catalyzed by a Ru/B-H Binary Catalyst System. Cheminform. 47. DOI: 10.1002/CHIN.201634035 |
0.814 |
|
| 2016 |
Bansode AH, Chimala P, Patil NT. Catalytic Branching Cascades in Diversity Oriented Synthesis Chemcatchem. 9: 30-40. DOI: 10.1002/Cctc.201600766 |
0.8 |
|
| 2015 |
Shaikh AC, Ranade DS, Thorat S, Maity A, Kulkarni PP, Gonnade RG, Munshi P, Patil NT. Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons. Chemical Communications (Cambridge, England). 51: 16115-8. PMID 26392327 DOI: 10.1039/C5Cc06351E |
0.731 |
|
| 2015 |
Inamdar SM, Shinde VS, Patil NT. Enantioselective cooperative catalysis. Organic & Biomolecular Chemistry. 13: 8116-62. PMID 26123696 DOI: 10.1039/C5Ob00986C |
0.497 |
|
| 2015 |
Bagle PN, Shinde VS, Patil NT. Robustness screen in enantioselective catalysis enabled generation of enantioenriched heterocyclic scaffolds in one pot. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 3580-4. PMID 25589289 DOI: 10.1002/Chem.201406045 |
0.833 |
|
| 2015 |
Bansode AH, Shaikh AC, Kavthe RD, Thorat S, Gonnade RG, Patil NT. Catalyst-dependent selectivity in the relay catalytic branching cascade. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 2319-23. PMID 25483407 DOI: 10.1002/Chem.201405736 |
0.812 |
|
| 2015 |
Shinde VS, Mane MV, Vanka K, Mallick A, Patil NT. Gold(I)/chiral Brønsted acid catalyzed enantioselective hydroamination-hydroarylation of alkynes: the effect of a remote hydroxyl group on the reactivity and enantioselectivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 975-9. PMID 25421270 DOI: 10.1002/Chem.201405061 |
0.775 |
|
| 2015 |
Shinde VS, Mane MV, Vanka K, Mallick A, Patil NT. Gold/Chiral Phosphoric Acid Catalyzed Hydroamination–Hydroarylation of Alkynes Synfacts. 11: 168-168. DOI: 10.1055/S-0034-1379780 |
0.744 |
|
| 2015 |
Inamdar SM, Patil NT. Engineering ligands on the Au center: Discovering broadly applicable gold catalysis with high turnover numbers Organic Chemistry Frontiers. 2: 995-998. DOI: 10.1039/C5Qo00162E |
0.486 |
|
| 2015 |
Shaikh AC, Shalini S, Vaidhyanathan R, Mane MV, Barui AK, Patra CR, Venkatesh Y, Bangal PR, Patil NT. Identifying Solid Luminogens through Gold-Catalysed Intramolecular Hydroarylation of Alkynes European Journal of Organic Chemistry. 2015: 4860-4867. DOI: 10.1002/Ejoc.201500503 |
0.82 |
|
| 2015 |
Shaikh AC, Shalini S, Vaidhyanathan R, Mane MV, Barui AK, Patra CR, Venkatesh Y, Bangal PR, Patil NT. ChemInform Abstract: Identifying Solid Luminogens Through Gold-Catalyzed Intramolecular Hydroarylation of Alkynes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201547158 |
0.824 |
|
| 2015 |
Inamdar SM, Patil NT. ChemInform Abstract: Engineering Ligands on the Au Center: Discovering Broadly Applicable Gold Catalysis with High Turnover Numbers. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201535293 |
0.335 |
|
| 2015 |
Mutyala AK, Patil NT. ChemInform Abstract: Enantioselective Heterogeneous Broensted Acid Catalysis Cheminform. 46. DOI: 10.1002/CHIN.201501252 |
0.318 |
|
| 2015 |
Bansode AH, Shaikh AC, Kavthe RD, Thorat S, Gonnade RG, Patil NT. Inside Back Cover: Catalyst-Dependent Selectivity in the Relay Catalytic Branching Cascade (Chem. Eur. J. 6/2015) Chemistry - a European Journal. 21: 2707-2707. DOI: 10.1002/Chem.201590023 |
0.793 |
|
| 2014 |
Inamdar SM, Konala A, Patil NT. When gold meets chiral Brønsted acid catalysts: extending the boundaries of enantioselective gold catalysis. Chemical Communications (Cambridge, England). 50: 15124-35. PMID 25177929 DOI: 10.1039/C4Cc04633A |
0.553 |
|
| 2014 |
Mutyala AK, Patil NT. Enantioselective heterogeneous Brønsted acid catalysis Org. Chem. Front.. 1: 582-586. DOI: 10.1039/C4Qo00051J |
0.461 |
|
| 2014 |
Patil NT. ChemInform Abstract: The Power of Gold Beyond Glitter: Homogeneous Catalysis with Au(I)-Complexes to Generate a Library of Privileged Scaffolds Cheminform. 45: no-no. DOI: 10.1002/CHIN.201405235 |
0.325 |
|
| 2013 |
Belgi A, Bathgate RA, Kocan M, Patil N, Zhang S, Tregear GW, Wade JD, Hossain MA. Minimum active structure of insulin-like peptide 5. Journal of Medicinal Chemistry. 56: 9509-16. PMID 24188028 DOI: 10.1021/jm400924p |
0.227 |
|
| 2013 |
Patil NT, Konala A, Sravanti S, Singh A, Ummanni R, Sridhar B. Electrophile induced branching cascade: a powerful approach to access various molecular scaffolds and their exploration as novel anti-mycobacterial agents. Chemical Communications (Cambridge, England). 49: 10109-11. PMID 24045420 DOI: 10.1039/C3Cc45289A |
0.384 |
|
| 2013 |
Patil NT, Shinde VS, Sridhar B. Relay catalytic branching cascade: a technique to access diverse molecular scaffolds. Angewandte Chemie (International Ed. in English). 52: 2251-5. PMID 23335120 DOI: 10.1002/Anie.201208738 |
0.428 |
|
| 2013 |
Patil NT, Raut VS, Tella RB. Enantioselective cooperative triple catalysis: unique roles of Au(I)/amine/chiral Brønsted acid catalysts in the addition/cycloisomerization/transfer hydrogenation cascade. Chemical Communications (Cambridge, England). 49: 570-2. PMID 23223156 DOI: 10.1039/C2Cc37623G |
0.51 |
|
| 2013 |
Patil NT, Kavthe RD, Shinde VS. ChemInform Abstract: Transition Metal Cataylzed Addition of C-, N- and O-Nucleophiles to Unactivated C-C Multiple Bonds Cheminform. 44: no-no. DOI: 10.1002/CHIN.201306173 |
0.316 |
|
| 2012 |
Patil NT, Shinde VS, Thakare MS, Hemant Kumar P, Bangal PR, Barui AK, Patra CR. Exploiting the higher alkynophilicity of Au-species: development of a highly selective fluorescent probe for gold ions. Chemical Communications (Cambridge, England). 48: 11229-31. PMID 23066526 DOI: 10.1039/C2Cc35083A |
0.383 |
|
| 2012 |
Patil NT, Nijamudheen A, Datta A. Aminoindolines versus quinolines: mechanistic insights into the reaction between 2-aminobenzaldehydes and terminal alkynes in the presence of metals and secondary amines. The Journal of Organic Chemistry. 77: 6179-85. PMID 22780441 DOI: 10.1021/Jo300949D |
0.525 |
|
| 2012 |
Patil NT. Chirality transfer and memory of chirality in gold-catalyzed reactions. Chemistry, An Asian Journal. 7: 2186-94. PMID 22674545 DOI: 10.1002/Asia.201200194 |
0.52 |
|
| 2012 |
Patil NT, Raut VS, Shinde VS, Gayatri G, Sastry GN. Gold(I)-catalyzed unprecedented rearrangement reaction between 2-aminobenzaldehydes with propargyl amines: an expedient route to 3-aminoquinolines. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5530-5. PMID 22434541 DOI: 10.1002/Chem.201103668 |
0.574 |
|
| 2012 |
Patil NT, Mutyala AK, Konala A, Tella RB. Tuning the reactivity of Au-complexes in an Au(I)/chiral Brønsted acid cooperative catalytic system: an approach to optically active fused 1,2-dihydroisoquinolines. Chemical Communications (Cambridge, England). 48: 3094-6. PMID 22344270 DOI: 10.1039/C2Cc17450B |
0.483 |
|
| 2012 |
Patil NT, Shinde VS, Gajula B. A one-pot catalysis: the strategic classification with some recent examples. Organic & Biomolecular Chemistry. 10: 211-24. PMID 22072256 DOI: 10.1039/C1Ob06432K |
0.438 |
|
| 2012 |
Patil NT, Kavthe RD, Shinde VS. Transition metal-catalyzed addition of C-, N- and O-nucleophiles to unactivated C–C multiple bonds Tetrahedron. 68: 8079-8146. DOI: 10.1016/J.Tet.2012.05.125 |
0.437 |
|
| 2012 |
Patil NT, Lakshmi PGVV, Sridhar B, Patra S, Pal Bhadra M, Patra CR. New Linearly and Angularly Fused Quinazolinones: Synthesis through Gold(I)-Catalyzed Cascade Reactions and Anticancer Activities European Journal of Organic Chemistry. 2012: 1790-1799. DOI: 10.1002/Ejoc.201101822 |
0.501 |
|
| 2012 |
Patil NT, Raut VS, Shinde VS, Gayatri G, Sastry GN. Gold(I)-catalyzed unprecedented rearrangement reaction between 2-aminobenzaldehydes with propargyl amines: An expedient route to 3-aminoquinolines Chemistry - a European Journal. 18: 5530-5535. DOI: 10.1002/chem.201103668 |
0.517 |
|
| 2012 |
Patil NT. Chirality transfer and memory of chirality in gold-catalyzed reactions Chemistry - An Asian Journal. 7: 2186-2194. DOI: 10.1002/asia.201200194 |
0.439 |
|
| 2011 |
Patil NT, Singh V. Synthesis of 1,3,5-trisubstituted pyrazolines via Zn(II)-catalyzed double hydroamination of enynes with aryl hydrazines. Chemical Communications (Cambridge, England). 47: 11116-8. PMID 21909551 DOI: 10.1039/c1cc14850h |
0.396 |
|
| 2011 |
Patil NT. Merging metal and N-heterocyclic carbene catalysis: on the way to discovering enantioselective organic transformations. Angewandte Chemie (International Ed. in English). 50: 1759-61. PMID 21271627 DOI: 10.1002/Anie.201006866 |
0.435 |
|
| 2011 |
Patil NT, Singh V. Alkyne hydroamination triggered cyclizations: A powerful tool for the construction of biologically important structural motifs Journal of Organometallic Chemistry. 696: 419-432. DOI: 10.1016/J.Jorganchem.2010.10.027 |
0.476 |
|
| 2011 |
Patil NT. ChemInform Abstract: Heterogeneous π-Acid Catalysis with Metal Nanoparticles Cheminform. 42: no-no. DOI: 10.1002/CHIN.201146229 |
0.313 |
|
| 2011 |
Patil NT, Konala A. ChemInform Abstract: Mechanistic Dichotomy with Alkynes in the Formal Hydrohydrazination/Fischer Indolization Tandem Reaction Catalyzed by a Ph3PAuNTf2/pTSA Binary System. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201116107 |
0.499 |
|
| 2011 |
Patil NT, Singh V. ChemInform Abstract: Alkyne Hydroamination Triggered Cyclizations: A Powerful Tool for the Construction of Biologically Important Structural Motifs Cheminform. 42: no-no. DOI: 10.1002/CHIN.201115231 |
0.286 |
|
| 2011 |
Patil NT. Heterogeneous π-Acid Catalysis with Metal Nanoparticles Chemcatchem. 3: 1121-1125. DOI: 10.1002/cctc.201100029 |
0.304 |
|
| 2011 |
Patil NT. Merging metal and N-heterocyclic carbene catalysis: On the way to discovering enantioselective organic transformations Angewandte Chemie - International Edition. 50: 1759-1761. DOI: 10.1002/anie.201006866 |
0.392 |
|
| 2011 |
Patil NT. Verschmelzung von Metall‐ und NHC‐Katalyse: auf dem Weg zur Entdeckung enantioselektiver organischer Transformationen Angewandte Chemie. 123: 1797-1799. DOI: 10.1002/Ange.201006866 |
0.3 |
|
| 2010 |
Patil NT, Raut VS. Cooperative catalysis with metal and secondary amine: synthesis of 2-substituted quinolines via addition/cycloisomerization cascade. The Journal of Organic Chemistry. 75: 6961-4. PMID 20857944 DOI: 10.1021/Jo101103A |
0.535 |
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| 2010 |
Patil NT, Mutyala AK, Lakshmi PG, Gajula B, Sridhar B, Pottireddygari GR, Rao TP. Au(I)-catalyzed cascade reaction involving formal double hydroamination of alkynes bearing tethered carboxylic groups: an easy access to fused dihydrobenzimidazoles and tetrahydroquinazolines. The Journal of Organic Chemistry. 75: 5963-75. PMID 20707335 DOI: 10.1021/jo1013228 |
0.529 |
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| 2010 |
Patil NT, Kavthe RD, Shinde VS, Sridhar B. Pt(IV)-catalyzed hydroamination triggered cyclization: a strategy to fused pyrrolo[1,2-a]quinoxalines, indolo[1,2-a]quinoxalines, and indolo[3,2-c]quinolines. The Journal of Organic Chemistry. 75: 3371-80. PMID 20392052 DOI: 10.1021/Jo100373W |
0.615 |
|
| 2010 |
Patil NT, Kavthe RD, Raut VS, Shinde VS, Sridhar B. Gold- and platinum-catalyzed formal Markownikoff's double hydroamination of alkynes: a rapid access to tetrahydroquinazolinones and angularly-fused analogues thereof. The Journal of Organic Chemistry. 75: 1277-80. PMID 20092269 DOI: 10.1021/Jo902293F |
0.529 |
|
| 2010 |
Patil N, Raut V. Metal/Amine Cooperative Catalysis. Heteroannulation Route to Quinolines Synfacts. 2011: 0025-0025. DOI: 10.1055/S-0030-1259201 |
0.33 |
|
| 2010 |
Patil NT, Kavthe RD, Yamamoto Y. Chapter 2 – Metal-Catalyzed Intramolecular Heteroatom (X) → Carbon (C) Functional Group Migration Reactions Involving Additions of X–Y Bonds Across Alkynes Advances in Heterocyclic Chemistry. 101: 75-95. DOI: 10.1016/S0065-2725(10)01002-0 |
0.661 |
|
| 2010 |
Patil NT, Singh V, Konala A, Mutyala AK. Gold(I)-catalyzed one-pot reaction between 2-alkynylanilines and alkynols leading to the formation of C-3-substituted indoles: a case of formal carboamination of alkynes Tetrahedron Letters. 51: 1493-1496. DOI: 10.1016/J.TETLET.2010.01.036 |
0.485 |
|
| 2010 |
Patil NT, Konala A. Mechanistic Dichotomy with Alkynes in the Formal Hydrohydrazination/Fischer Indolization Tandem Reaction Catalyzed by a Ph3PAuNTf2/pTSA Binary System European Journal of Organic Chemistry. 2010: 6831-6839. DOI: 10.1002/Ejoc.201001114 |
0.561 |
|
| 2010 |
Patil NT, Lakshmi PGVV, Singh V. AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes European Journal of Organic Chemistry. 2010: 4719-4731. DOI: 10.1002/EJOC.201000389 |
0.414 |
|
| 2010 |
Patil NT, Mutyala AK, Lakshmi PGVV, Raju PVK, Sridhar B. Facile Assembly of Fused Isoquinolines by Gold(I)-Catalyzed Coupling-Cyclization Reactions between o-Alkynylbenzaldehydes and Aromatic Amines Containing Tethered Nucleophiles European Journal of Organic Chemistry. 2010: 1999-2007. DOI: 10.1002/EJOC.200901364 |
0.465 |
|
| 2010 |
Patil NT, Lakshmi PGVV, Singh V. ChemInform Abstract: AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201052176 |
0.412 |
|
| 2010 |
Patil NT, Kavthe RD, Yamamoto Y. ChemInform Abstract: Metal-Catalyzed Intramolecular Heteroatom (X) → Carbon (C) Functional Group Migration Reactions Involving Additions of X-Y Bonds Across Alkynes Cheminform. 41: no-no. DOI: 10.1002/chin.201051247 |
0.515 |
|
| 2010 |
Patil NT, Yamamoto Y. ChemInform Abstract: Transition Metal Catalyzed Cyclization Reactions of Functionalized Alkenes, Alkynes, and Allenes Cheminform. 41: no-no. DOI: 10.1002/chin.201037257 |
0.567 |
|
| 2010 |
Patil NT, Mutyala AK, Lakshmi PGVV, Raju PVK, Sridhar B. ChemInform Abstract: Facile Assembly of Fused Isoquinolines by Gold(I)-Catalyzed Coupling-Cyclization Reactions Between o-Alkynylbenzaldehydes and Aromatic Amines Containing Tethered Nucleophiles. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201035161 |
0.468 |
|
| 2010 |
Patil NT, Singh V, Konala A, Mutyala AK. ChemInform Abstract: Gold(I)-Catalyzed One-Pot Reaction Between 2-Alkynylanilines and Alkynols Leading to the Formation of C-3-Substituted Indoles: A Case of Formal Carboamination of Alkynes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201027101 |
0.488 |
|
| 2010 |
Patil NT, Raut VS, Kavthe RD, Reddy VVN, Raju PVK. ChemInform Abstract: Thorpe-Ingold Effect in Copper(II)-Catalyzed Formal Hydroalkoxylation-Hydroarylation Reaction of Alkynols with Indoles. Cheminform. 41. DOI: 10.1002/CHIN.201010115 |
0.421 |
|
| 2010 |
Patil NT, Konala A, Singh V, Reddy VVN. ChemInform Abstract: Highly Selective Electrophile-Induced Cascade Reactions Between o-Alkynylbenzaldehydes and Styrene Oxides Leading to the Formation of 1-Naphthyl Ketones. Cheminform. 41. DOI: 10.1002/CHIN.201006086 |
0.399 |
|
| 2009 |
Patil NT, Kavthe RD, Raut VS, Reddy VV. Platinum-catalyzed formal Markownikoff's hydroamination/hydroarylation cascade of terminal alkynes assisted by tethered hydroxyl groups. The Journal of Organic Chemistry. 74: 6315-8. PMID 20560573 DOI: 10.1021/Jo901200J |
0.549 |
|
| 2009 |
Yamamoto Y, Gridnev ID, Patil NT, Jin T. Alkyne activation with Brønsted acids, iodine, or gold complexes, and its fate leading to synthetic application. Chemical Communications (Cambridge, England). 5075-87. PMID 20448954 DOI: 10.1039/B909978F |
0.654 |
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| 2009 |
Fischer D, Tomeba H, Pahadi NK, Patil NT, Huo Z, Yamamoto Y. Synthesis of Isoquinolines by I2-Mediated ElectrophilicHeteroannulation Synfacts. 2009: 137-137. DOI: 10.1055/S-0028-1087575 |
0.558 |
|
| 2009 |
Patil NT, Raut VS, Kavthe RD, Reddy VV, Raju P. Thorpe–Ingold effect in copper(II)-catalyzed formal hydroalkoxylation–hydroarylation reaction of alkynols with indoles Tetrahedron Letters. 50: 6576-6579. DOI: 10.1016/J.Tetlet.2009.09.057 |
0.555 |
|
| 2009 |
Patil NT, Konala A, Singh V, Reddy VVN. Highly Selective Electrophile-Induced Cascade Reactions betweeno-Alkynylbenzaldehydes and Styrene Oxides Leading to the Formation of 1-Naphthyl Ketones European Journal of Organic Chemistry. 2009: 5178-5184. DOI: 10.1002/EJOC.200900809 |
0.422 |
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| 2008 |
Fischer D, Tomeba H, Pahadi NK, Patil NT, Huo Z, Yamamoto Y. Iodine-mediated electrophilic cyclization of 2-alkynyl-1-methylene azide aromatics leading to highly substituted isoquinolines and its application to the synthesis of norchelerythrine. Journal of the American Chemical Society. 130: 15720-5. PMID 18942781 DOI: 10.1021/Ja805326F |
0.616 |
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| 2008 |
Patil NT, Yamamoto Y. Coinage metal-assisted synthesis of heterocycles. Chemical Reviews. 108: 3395-442. PMID 18611054 DOI: 10.1021/Cr050041J |
0.548 |
|
| 2007 |
Patil NT, Wu H, Yamamoto Y. A route to 2-substituted tetrahydroquinolines via palladium-catalyzed intramolecular hydroamination of anilino-alkynes. The Journal of Organic Chemistry. 72: 6577-9. PMID 17636960 DOI: 10.1021/Jo0708137 |
0.619 |
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| 2007 |
Fischer D, Tomeba H, Pahadi NK, Patil NT, Yamamoto Y. Synthesis of 1,3,4-trisubstituted isoquinolines by iodine-mediated electrophilic cyclization of 2-alkynyl benzyl azides. Angewandte Chemie (International Ed. in English). 46: 4764-6. PMID 17516604 DOI: 10.1002/Anie.200701392 |
0.609 |
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| 2007 |
Patil NT, Yamamoto Y. Metal-Mediated Synthesis of Furans and Pyrroles Cheminform. 38. DOI: 10.3998/Ark.5550190.0008.A11 |
0.587 |
|
| 2007 |
Patil NT, Yamamoto Y. Metal-mediated synthesis of furans and pyrroles Arkivoc. 2007: 121-141. DOI: 10.3998/ARK.5550190.0008.A11 |
0.342 |
|
| 2007 |
Patil NT, Yamamoto Y. Gold-Catalyzed Reactions of Oxoalkynes Cheminform. 38. DOI: 10.3998/Ark.5550190.0008.502 |
0.684 |
|
| 2007 |
Patil NT, Wu H, Yamamoto Y. Palladium-Catalyzed Hydroamination Route to 2-Substituted Tetrahydroquinolines Synfacts. 2007: 1139-1139. DOI: 10.1055/S-2007-991301 |
0.537 |
|
| 2007 |
Yamamoto Y, Patil N. Palladium-Catalyzed Cascade Reactions of Highly Activated Olefins Synlett. 2007: 1994-2005. DOI: 10.1055/S-2007-984892 |
0.614 |
|
| 2007 |
Fischer D, Tomeba H, Pahadi NK, Patil NT, Yamamoto Y. Transition-Metal-Free Synthesis of Isoquinolines Synfacts. 2007: 911-911. DOI: 10.1055/S-2007-968904 |
0.518 |
|
| 2007 |
Patil NT, Huo Z, Yamamoto Y. Palladium catalyzed three component coupling reaction between chromones, alcohols, and allylic acetates: diversity-oriented synthesis of highly substituted chromones Tetrahedron. 63: 5954-5961. DOI: 10.1016/J.Tet.2007.02.110 |
0.562 |
|
| 2007 |
Patil NT, Yamamoto Y. Palladium-Catalyzed Cascade Reactions of Highly Activated Olefins Cheminform. 38. DOI: 10.1002/chin.200745246 |
0.603 |
|
| 2007 |
Patil NT, Huo Z, Yamamoto Y. Palladium-Catalyzed Three-Component Coupling Reaction Between Chromones, Alcohols, and Allylic Acetates: Diversity-Oriented Synthesis of Highly Substituted Chromones. Cheminform. 38. DOI: 10.1002/CHIN.200740138 |
0.452 |
|
| 2007 |
Huo Z, Patil NT, Jin T, Pahadi NK, Yamamoto Y. Suppression of β-Hydride Elimination in the Intramolecular Hydrocarboxylation of Alkynes Leading to the Formation of Lactones. Cheminform. 38. DOI: 10.1002/CHIN.200729091 |
0.284 |
|
| 2007 |
Patil NT, Yamamoto Y. Palladium-Catalyzed Cascade Reactions Involving π-Allyl Palladium Chemistry Cheminform. 38. DOI: 10.1002/chin.200704227 |
0.627 |
|
| 2007 |
Huo Z, Patil N, Jin T, Pahadi N, Yamamoto Y. Suppression of β-Hydride Elimination in the Intramolecular Hydrocarboxylation of Alkynes leading to the Formation of Lactones Advanced Synthesis & Catalysis. 349: 680-684. DOI: 10.1002/Adsc.200600507 |
0.576 |
|
| 2006 |
Patil NT, Huo Z, Yamamoto Y. Palladium-catalyzed decarboxylative aza-Michael addition-allylation reactions between allyl carbamates and activated olefins. Generation of quaternary carbon adjacent to secondary amine carbon center. The Journal of Organic Chemistry. 71: 6991-5. PMID 16930053 DOI: 10.1021/Jo061110C |
0.582 |
|
| 2006 |
Patil NT, Lutete LM, Wu H, Pahadi NK, Gridnev ID, Yamamoto Y. Palladium-catalyzed intramolecular asymmetric hydroamination, hydroalkoxylation, and hydrocarbonation of alkynes. The Journal of Organic Chemistry. 71: 4270-9. PMID 16709071 DOI: 10.1021/Jo0603835 |
0.671 |
|
| 2006 |
Patil NT, Huo Z, Bajracharya GB, Yamamoto Y. Lactam synthesis via the intramolecular hydroamidation of alkynes catalyzed by palladium complexes. The Journal of Organic Chemistry. 71: 3612-4. PMID 16626149 DOI: 10.1021/Jo060142X |
0.815 |
|
| 2006 |
Patil NT, Huo Z, Yamamoto Y. Beta-alkyl-alpha-allylation of Michael acceptors through the palladium-catalyzed three-component coupling between allylic substrates, trialkylboranes, and activated olefins. The Journal of Organic Chemistry. 71: 2503-6. PMID 16526804 DOI: 10.1021/Jo0524876 |
0.565 |
|
| 2006 |
Patil NT, Yamamoto Y. Gold-catalyzed reactions of oxo-alkynes Arkivoc. 2007: 6-19. DOI: 10.3998/ARK.5550190.0008.502 |
0.504 |
|
| 2006 |
Yamamoto Y, Patil N, Lutete L, Wu H, Pahadi N, Gridnev I. Asymmetric Synthesis of O- and N-Heterocycles by Intramolecular Hydroamination and -alkoxylation Synfacts. 2006: 0892-0892. DOI: 10.1055/S-2006-942064 |
0.547 |
|
| 2006 |
Patil NT, Lutete LM, Nishina N, Yamamoto Y. Gold-catalyzed intramolecular hydroamination of allenes: a case of chirality transfer Tetrahedron Letters. 47: 4749-4751. DOI: 10.1016/J.Tetlet.2006.04.087 |
0.624 |
|
| 2006 |
Patil NT, Song D, Yamamoto Y. Palladium-Catalyzed Allylation of Pronucleophiles with Alkynes at 50 °C – Remarkable Effect of 2-(Dicyclohexylphosphanyl)-2′-(dimethylamino)biphenyl as Ligand European Journal of Organic Chemistry. 2006: 4211-4213. DOI: 10.1002/Ejoc.200600337 |
0.539 |
|
| 2006 |
Patil NT, Song D, Yamamoto Y. Palladium-Catalyzed Allylation of Pronucleophiles with Alkynes at 50 °C — Remarkable Effect of 2-(Dicyclohexylphosphanyl)-2′-(dimethylamino)biphenyl as Ligand. Cheminform. 37. DOI: 10.1002/chin.200652053 |
0.514 |
|
| 2006 |
Patil NT, Lutete LM, Nishina N, Yamamoto Y. Gold-Catalyzed Intramolecular Hydroamination of Allenes: A Case of Chirality Transfer. Cheminform. 37. DOI: 10.1002/chin.200642105 |
0.515 |
|
| 2006 |
Patil NT, Yamamoto Y. Progress in the Total Synthesis of Laurencin and Prelaureatin Cheminform. 37. DOI: 10.1002/chin.200629262 |
0.483 |
|
| 2006 |
Patil NT, Pahadi NK, Yamamoto Y. Pd(0)-PhCOOH Catalyzed Addition of Oxygen Pronucleophiles to Allenes and Internal Alkynes. Cheminform. 37. DOI: 10.1002/chin.200612036 |
0.433 |
|
| 2005 |
Patil NT, Pahadi NK, Yamamoto Y. Silver(I)-catalyzed novel cascade cyclization reactions: incorporation of allenes into the isochromenes. The Journal of Organic Chemistry. 70: 10096-8. PMID 16292845 DOI: 10.1021/Jo051524Q |
0.623 |
|
| 2005 |
Patil NT, Wu H, Yamamoto Y. Cu(I) catalyst in DMF: an efficient catalytic system for the synthesis of furans from 2-(1-alkynyl)-2-alken-1-ones. The Journal of Organic Chemistry. 70: 4531-4. PMID 15903340 DOI: 10.1021/Jo050191U |
0.641 |
|
| 2005 |
Patil NT, Pahadi NK, Yamamoto Y. Pd(0)PhCOOH catalyzed addition of oxygen pronucleophiles to allenes and internal alkynes Canadian Journal of Chemistry. 83: 569-573. DOI: 10.1139/V05-043 |
0.593 |
|
| 2005 |
Patil NT, Pahadi NK, Yamamoto Y. A new route for the synthesis of indolizidine (−)-209D: excellent diastereoselectivity in the intramolecular hydroamination of alkynes Tetrahedron Letters. 46: 2101-2103. DOI: 10.1016/J.Tetlet.2005.01.139 |
0.608 |
|
| 2005 |
Patil NT, Khan FN, Yamamoto Y. Microwave-Enhanced Pd(0)/Acetic Acid Catalyzed Allylation Reactions of C, N, and O-Pronucleophiles with Alkynes. Cheminform. 36. DOI: 10.1002/chin.200508043 |
0.53 |
|
| 2005 |
Patil NT, Pahadi NK, Yamamoto Y. An Improved Catalytic System, Pd(PPh3)4/PhCOOH Combined Catalyst, for the Allylation of Carbon Pronucleophiles with Allenes. Cheminform. 36. DOI: 10.1002/chin.200504054 |
0.486 |
|
| 2004 |
Patil NT, Wu H, Kadota I, Yamamoto Y. A convenient and efficient route for the allylation of aromatic amines and alpha-aryl aldehydes with alkynes in the presence of a Pd(0)/PhCOOH combined catalyst system. The Journal of Organic Chemistry. 69: 8745-50. PMID 15575752 DOI: 10.1021/Jo0485684 |
0.812 |
|
| 2004 |
Patil NT, Yamamoto Y. Formation of a quaternary carbon center through the Pd(0)/PhCOOH-catalyzed allylation of cyclic beta-keto esters and 1,3-diketones with alkynes. The Journal of Organic Chemistry. 69: 6478-81. PMID 15357613 DOI: 10.1021/Jo0490144 |
0.568 |
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| 2004 |
Patil NT, Yamamoto Y. Synthesis of cyclic alkenyl ethers via intramolecular cyclization of O-alkynylbenzaldehydes. Importance of combination between CuI catalyst and DMF. The Journal of Organic Chemistry. 69: 5139-42. PMID 15255753 DOI: 10.1021/Jo049416B |
0.642 |
|
| 2004 |
Yamamoto Y, Patil NT, Pahadi NK. An Improved Catalytic System, Pd(PPh3)4/PhCOOH Combined Catalyst, for the Allylation of Carbon Pronucleophiles with Allenes Synthesis. 2004: 2186-2190. DOI: 10.1055/S-2004-829178 |
0.598 |
|
| 2004 |
Patil NT, Nawaz Khan F, Yamamoto Y. Microwave-enhanced Pd(0)/acetic acid catalyzed allylation reactions of C, N, and O-pronucleophiles with alkynes Tetrahedron Letters. 45: 8497-8499. DOI: 10.1016/J.Tetlet.2004.09.099 |
0.614 |
|
| 2004 |
Patil NT, Yamamoto Y. Direct allylic substitution of allyl alcohols by carbon pronucleophiles in the presence of a palladium/carboxylic acid catalyst under neat conditions Tetrahedron Letters. 45: 3101-3103. DOI: 10.1016/J.Tetlet.2004.02.094 |
0.588 |
|
| 2004 |
Patil NT, Yamamoto Y. Direct Allylic Substitution of Allyl Alcohols by Carbon Pronucleophiles in the Presence of a Palladium/Carboxylic Acid Catalyst under Neat Conditions. Cheminform. 35. DOI: 10.1002/chin.200430053 |
0.51 |
|
| 2004 |
Patil N, Kadota I, Shibuya A, Gyoung Y, Yamamoto Y. Allylation of Carbon Pronucleophiles with Alkynes in the Presence of Palladium/Acetic Acid Catalyst Advanced Synthesis & Catalysis. 346: 800-804. DOI: 10.1002/Adsc.200404046 |
0.629 |
|
| 2003 |
Tilekar JN, Patil NT, Jadhav HS, Dhavale DD. Concise and practical synthesis of (2S,3R,4R,5R) and (2S,3R,4R,5S)-1,6-dideoxy-1,6-iminosugars Tetrahedron. 59: 1873-1876. DOI: 10.1016/S0040-4020(03)00177-7 |
0.669 |
|
| 2002 |
Patil NT, John S, Sabharwal SG, Dhavale DD. 1-Aza-sugars from D-glucose. Preparation of 1-deoxy-5-dehydroxymethyl-nojirimycin, its analogues and evaluation of glycosidase inhibitory activity. Bioorganic & Medicinal Chemistry. 10: 2155-60. PMID 11983511 DOI: 10.1016/S0968-0896(02)00073-1 |
0.69 |
|
| 2001 |
Patil NT, Tilekar JN, Dhavale DD. Intermolecular Michael addition of substituted amines to a sugar-derived alpha,beta-unsaturated ester: synthesis of 1-deoxy-D-gluco- and -L-ido-homonojirimycin, 1-deoxy-castanospermine and 1-deoxy-8a-epi-castanospermine. The Journal of Organic Chemistry. 66: 1065-74. PMID 11312931 DOI: 10.1021/Jo0010476 |
0.682 |
|
| 2001 |
Patil NT, Tilekar JN, Dhavale DD. A short and efficient synthesis of 1-deoxy-castanospermine and 1-deoxy-8a-epi-castanospermine Tetrahedron Letters. 42: 747-749. DOI: 10.1016/S0040-4039(00)02103-1 |
0.707 |
|
| 2000 |
Tilekar JN, Patil NT, Dhavale DD. Synthesis of C1-C6 Segment of Carbonolide B: Wolff Rearrangement of Sugar α-Diazo Ketones Synthesis. 2000: 395-398. DOI: 10.1055/S-2000-6343 |
0.712 |
|
| 2000 |
Tilekar JN, Patil NT, Dhavale DD. Synthesis of C1-C6 segment of carbonolide B: Wolff rearrangement of sugar α-diazo ketones Synthesis. 395-398. |
0.692 |
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