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Material Type: Article
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Rhodium or Ruthenium-Catalyzed Oxidative CH/CH Cross-Coupling: Direct Access to Extended π-Conjugated SystemsAngewandte Chemie (International ed.), 2013-01, Vol.52 (2), p.580-584 [Peer Reviewed Journal]Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201207196 ;PMID: 23184621Full text available |
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Material Type: Article
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Catalytic Organometallic Reactions of AmmoniaAngewandte Chemie (International ed.), 2011-01, Vol.50 (1), p.86-95 [Peer Reviewed Journal]Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright Wiley Subscription Services, Inc. Jan 2011 ;2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2011 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201002354 ;PMID: 20857466 ;CODEN: ACIEAYFull text available |
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Material Type: Article
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Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactionsMolecules, 2010-03, Vol.15 (4), p.2124-2138 [Peer Reviewed Journal]Copyright MDPI AG 2010 ;2010 by the authors; 2010 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules15042124 ;PMID: 20428032Full text available |
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Material Type: Article
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Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Arylsulfinates with H-Phosphonate DiestersAdvanced synthesis & catalysis, 2014-03, Vol.356 (5), p.967-971 [Peer Reviewed Journal]2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201300983Full text available |
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5 |
Material Type: Article
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High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical OverviewAdvanced synthesis & catalysis, 2004-12, Vol.346 (13-15), p.1553-1582 [Peer Reviewed Journal]Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.200404178Full text available |
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Material Type: Article
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N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactionsBeilstein journal of organic chemistry, 2016-01, Vol.12 (1), p.81-88 [Peer Reviewed Journal]Copyright © 2016, Akkoç et al; licensee Beilstein-Institut. This work is licensed under the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2016, Akkoç et al. 2016 Akkoç et al. ;ISSN: 1860-5397 ;ISSN: 2195-951X ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.12.9 ;PMID: 26877810Full text available |
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Material Type: Article
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Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot CatalystsCatalysts, 2022-06, Vol.12 (6), p.619 [Peer Reviewed Journal]2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2073-4344 ;EISSN: 2073-4344 ;DOI: 10.3390/catal12060619Full text available |
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Material Type: Article
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A Triptycene-Based Microporous Organic Polymer Bearing Tridentate Ligands and Its Application in Suzuki-Miyaura Cross-Coupling ReactionMacromolecular rapid communications., 2015-02, Vol.36 (4), p.413-418 [Peer Reviewed Journal]2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1022-1336 ;EISSN: 1521-3927 ;DOI: 10.1002/marc.201400593 ;PMID: 25639593Full text available |
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Material Type: Article
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Recent Advances in Catalytic Alkyne Transformation via Copper Carbene IntermediatesMolecules (Basel, Switzerland), 2022-05, Vol.27 (10), p.3088 [Peer Reviewed Journal]2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules27103088 ;PMID: 35630567Full text available |
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Material Type: Article
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Transition metal-catalyzed decarboxylative cross-coupling reactionsScience China. Chemistry, 2011-11, Vol.54 (11), p.1670-1687 [Peer Reviewed Journal]Science China Press and Springer-Verlag Berlin Heidelberg 2011 ;Science China Press and Springer-Verlag Berlin Heidelberg 2011. ;ISSN: 1674-7291 ;EISSN: 1869-1870 ;DOI: 10.1007/s11426-011-4381-0Full text available |
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11 |
Material Type: Article
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Element−Element Additions to Unsaturated Carbon−Carbon Bonds Catalyzed by Transition Metal ComplexesChemical reviews, 2006-06, Vol.106 (6), p.2320-2354 [Peer Reviewed Journal]Copyright © 2006 American Chemical Society ;ISSN: 0009-2665 ;ISSN: 1520-6890 ;EISSN: 1520-6890 ;DOI: 10.1021/cr050530j ;PMID: 16771452 ;CODEN: CHREAYFull text available |
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12 |
Material Type: Article
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Copper-catalyzed C(sp2)-C(sp) Sonogashira-type cross-coupling reactions accelerated by polycyclic aromatic hydrocarbonsApplied organometallic chemistry, 2015-06, Vol.29 (6), p.353-356 [Peer Reviewed Journal]Copyright © 2015 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3298Full text available |
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Material Type: Article
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Polyvinylpyridine-Supported Palladium Nanoparticles: A Valuable Catalyst for the Synthesis of Alkynyl Ketones via Acyl Sonogashira ReactionsCatalysis letters, 2020-03, Vol.150 (3), p.652-659 [Peer Reviewed Journal]Springer Science+Business Media, LLC, part of Springer Nature 2019 ;COPYRIGHT 2020 Springer ;Catalysis Letters is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 1011-372X ;EISSN: 1572-879X ;DOI: 10.1007/s10562-019-02959-5Full text available |
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Material Type: Article
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A versatile method for the synthesis of diaryl and alkyl aryl ketones via palladium-catalysed cross-coupling reaction of arylboronic acids with acyl chloridesApplied organometallic chemistry, 2015-03, Vol.29 (3), p.181-184 [Peer Reviewed Journal]Copyright © 2015 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3269Full text available |
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Material Type: Article
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Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromidesApplied organometallic chemistry, 2014-07, Vol.28 (7), p.529-536 [Peer Reviewed Journal]Copyright © 2014 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3158Full text available |
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Material Type: Article
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Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling ReactionMolecules (Basel, Switzerland), 2022-01, Vol.27 (3), p.967 [Peer Reviewed Journal]2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules27030967 ;PMID: 35164232Full text available |
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17 |
Material Type: Article
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Cobalt-Catalyzed Cross-Coupling Reactions of Alkyl Halides with Allylic and Benzylic Grignard Reagents and Their Application to Tandem Radical Cyclization/Cross-Coupling ReactionsChemistry : a European journal, 2004-11, Vol.10 (22), p.5640-5648 [Peer Reviewed Journal]Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.200400545 ;PMID: 15457521Full text available |
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18 |
Material Type: Article
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Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling ReactionCatalysis letters, 2022-06, Vol.152 (6), p.1621-1638 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 ;The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021. ;ISSN: 1011-372X ;EISSN: 1572-879X ;DOI: 10.1007/s10562-021-03755-wFull text available |
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19 |
Material Type: Article
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Carbon–Carbon Bond Formation for the Synthesis of 5-Aryl-2-Substituted Furans Catalyzed by K3[Fe(CN)6]Catalysis letters, 2022-08, Vol.152 (8), p.2288-2292 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 ;The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021. ;ISSN: 1011-372X ;EISSN: 1572-879X ;DOI: 10.1007/s10562-021-03799-yFull text available |
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20 |
Material Type: Article
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An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acidsBeilstein journal of organic chemistry, 2022-11, Vol.18, p.1518-1523 [Peer Reviewed Journal]Copyright Beilstein-Institut zur Föerderung der Chemischen Wissenschaften 2022 ;Copyright © 2022, Shearan et al. 2022 Shearan et al. ;ISSN: 1860-5397 ;ISSN: 2195-951X ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.18.160Full text available |