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1
Rhodium or Ruthenium-Catalyzed Oxidative CH/CH Cross-Coupling: Direct Access to Extended π-Conjugated Systems
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Rhodium or Ruthenium-Catalyzed Oxidative CH/CH Cross-Coupling: Direct Access to Extended π-Conjugated Systems

Angewandte 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: 23184621

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2
Catalytic Organometallic Reactions of Ammonia
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Catalytic Organometallic Reactions of Ammonia

Angewandte 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: ACIEAY

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3
Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions
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Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions

Molecules, 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: 20428032

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4
Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Arylsulfinates with H-Phosphonate Diesters
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Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Arylsulfinates with H-Phosphonate Diesters

Advanced 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.201300983

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5
High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview
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High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview

Advanced 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.200404178

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6
N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactions
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N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactions

Beilstein 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: 26877810

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7
Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot Catalysts
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Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot Catalysts

Catalysts, 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/catal12060619

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8
A Triptycene-Based Microporous Organic Polymer Bearing Tridentate Ligands and Its Application in Suzuki-Miyaura Cross-Coupling Reaction
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A Triptycene-Based Microporous Organic Polymer Bearing Tridentate Ligands and Its Application in Suzuki-Miyaura Cross-Coupling Reaction

Macromolecular 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: 25639593

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9
Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates
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Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates

Molecules (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: 35630567

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10
Transition metal-catalyzed decarboxylative cross-coupling reactions
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Transition metal-catalyzed decarboxylative cross-coupling reactions

Science 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/s11426-011-4381-0

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11
Element−Element Additions to Unsaturated Carbon−Carbon Bonds Catalyzed by Transition Metal Complexes
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Element−Element Additions to Unsaturated Carbon−Carbon Bonds Catalyzed by Transition Metal Complexes

Chemical 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: CHREAY

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12
Copper-catalyzed C(sp2)-C(sp) Sonogashira-type cross-coupling reactions accelerated by polycyclic aromatic hydrocarbons
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Copper-catalyzed C(sp2)-C(sp) Sonogashira-type cross-coupling reactions accelerated by polycyclic aromatic hydrocarbons

Applied 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.3298

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13
Polyvinylpyridine-Supported Palladium Nanoparticles: A Valuable Catalyst for the Synthesis of Alkynyl Ketones via Acyl Sonogashira Reactions
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Polyvinylpyridine-Supported Palladium Nanoparticles: A Valuable Catalyst for the Synthesis of Alkynyl Ketones via Acyl Sonogashira Reactions

Catalysis 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/s10562-019-02959-5

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14
A versatile method for the synthesis of diaryl and alkyl aryl ketones via palladium-catalysed cross-coupling reaction of arylboronic acids with acyl chlorides
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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 chlorides

Applied 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.3269

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15
Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides
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Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides

Applied 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.3158

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16
Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction
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Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction

Molecules (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: 35164232

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17
Cobalt-Catalyzed Cross-Coupling Reactions of Alkyl Halides with Allylic and Benzylic Grignard Reagents and Their Application to Tandem Radical Cyclization/Cross-Coupling Reactions
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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 Reactions

Chemistry : 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: 15457521

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18
Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling Reaction
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Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling Reaction

Catalysis 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-w

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19
Carbon–Carbon Bond Formation for the Synthesis of 5-Aryl-2-Substituted Furans Catalyzed by K3[Fe(CN)6]
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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-y

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20
An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids
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An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids

Beilstein 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.18.160

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