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1
Product molecule numbers and reaction rate fluctuations in elementary reactions
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Product molecule numbers and reaction rate fluctuations in elementary reactions

AIP advances, 2022-06, Vol.12 (6), p.065308-065308-7 [Peer Reviewed Journal]

Author(s) ;2022 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). ;ISSN: 2158-3226 ;EISSN: 2158-3226 ;DOI: 10.1063/5.0091597 ;CODEN: AAIDBI

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2
Recent advances in photoredox and nickel dual-catalyzed cascade reactions: pushing the boundaries of complexity
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Recent advances in photoredox and nickel dual-catalyzed cascade reactions: pushing the boundaries of complexity

Chemical science (Cambridge), 2020-04, Vol.11 (16), p.451-464 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry 2020. ;Copyright Royal Society of Chemistry 2020 ;This journal is © The Royal Society of Chemistry 2020 2020 ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d0sc00712a ;PMID: 32864080

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3
Biomimetic nanoflowers by self-assembly of nanozymes to induce intracellular oxidative damage against hypoxic tumors
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Biomimetic nanoflowers by self-assembly of nanozymes to induce intracellular oxidative damage against hypoxic tumors

Nature communications, 2018-08, Vol.9 (1), p.3334-14, Article 3334 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-05798-x ;PMID: 30127408

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4
In vivo three-dimensional multispectral photoacoustic imaging of dual enzyme-driven cyclic cascade reaction for tumor catalytic therapy
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In vivo three-dimensional multispectral photoacoustic imaging of dual enzyme-driven cyclic cascade reaction for tumor catalytic therapy

Nature communications, 2022-03, Vol.13 (1), p.1298-1298, Article 1298 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-022-29082-1 ;PMID: 35277519

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5
Editorial corner – a personal view
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Editorial corner – a personal view

Express polymer letters, 2021-02, Vol.15 (2), p.88-88 [Peer Reviewed Journal]

2021. This work is published under http://www.expresspolymlett.com/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 1788-618X ;DOI: 10.3144/expresspolymlett.2021.9

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6
Universal motifs and the diversity of autocatalytic systems
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Universal motifs and the diversity of autocatalytic systems

Proceedings of the National Academy of Sciences - PNAS, 2020-10, Vol.117 (41), p.25230-25236 [Peer Reviewed Journal]

Copyright National Academy of Sciences Oct 13, 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;2020 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2013527117 ;PMID: 32989134

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7
Functionalization of remote C(sp 3 )-H bonds enabled by copper-catalyzed coupling of O-acyloximes with terminal alkynes
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Functionalization of remote C(sp 3 )-H bonds enabled by copper-catalyzed coupling of O-acyloximes with terminal alkynes

Nature communications, 2020-01, Vol.11 (1), p.403-403, Article 403 [Peer Reviewed Journal]

This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-14292-2 ;PMID: 31964870

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8
Environmentally friendly domino multicomponent strategy for the synthesis of pyrroloquinolinone hybrid heterocycles
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Environmentally friendly domino multicomponent strategy for the synthesis of pyrroloquinolinone hybrid heterocycles

RSC advances, 2022-05, Vol.12 (24), p.1544-15446 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2022 ;This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d2ra02851d ;PMID: 35685174

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9
Salient features of the aza -Wacker cyclization reaction
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Salient features of the aza -Wacker cyclization reaction

Chemical science (Cambridge), 2020-07, Vol.11 (31), p.8073-8088 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2020 ;This journal is © The Royal Society of Chemistry 2020 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d0sc02554b ;PMID: 34123081

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10
LIGHTS, CHEMICAL REACTION! PLASTICS SHAPE UP UNDER UV
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LIGHTS, CHEMICAL REACTION! PLASTICS SHAPE UP UNDER UV

Nature (London), 2022-11, Vol.611 (7937), p.638-638 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 24, 2022 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/d41586-022-03709-1

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11
Correction: Siódmiak et al. The High ‘Lipolytic Jump’ of Immobilized Amano A Lipase from Aspergillus niger in Developed ‘ESS Catalytic Triangles’ Containing Natural Origin Substrates. Catalysts 2022, 12, 853
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Correction: Siódmiak et al. The High ‘Lipolytic Jump’ of Immobilized Amano A Lipase from Aspergillus niger in Developed ‘ESS Catalytic Triangles’ Containing Natural Origin Substrates. Catalysts 2022, 12, 853

Catalysts, 2023-02, Vol.13 (3), p.480 [Peer Reviewed Journal]

2023 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/catal13030480

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12
Correction: Costa et al. Glycerol and Catalysis by Waste/Low-Cost Materials—A Review. Catalysts 2022, 12, 570
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Correction: Costa et al. Glycerol and Catalysis by Waste/Low-Cost Materials—A Review. Catalysts 2022, 12, 570

Catalysts, 2023-02, Vol.13 (3), p.470 [Peer Reviewed Journal]

2023 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/catal13030470

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13
Efficient Biocatalytic System for Biosensing by Combining Metal–Organic Framework (MOF)-Based Nanozymes and G-Quadruplex (G4)-DNAzymes
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Efficient Biocatalytic System for Biosensing by Combining Metal–Organic Framework (MOF)-Based Nanozymes and G-Quadruplex (G4)-DNAzymes

Analytical chemistry (Washington), 2022-05, Vol.94 (20), p.7295-7302 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0003-2700 ;EISSN: 1520-6882 ;DOI: 10.1021/acs.analchem.2c00600 ;PMID: 35549161

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14
Modeling Chemical Reactions in Classical Molecular Dynamics Simulations
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Modeling Chemical Reactions in Classical Molecular Dynamics Simulations

Polymer (Guilford), 2017-10, Vol.128 [Peer Reviewed Journal]

Copyright Determination: PUBLIC_USE_PERMITTED ;ISSN: 0032-3861 ;EISSN: 1873-2291 ;DOI: 10.1016/j.polymer.2017.09.038

Digital Resources/Online E-Resources

15
The Reaction Mechanism Study for the F[sub.3] System
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The Reaction Mechanism Study for the F[sub.3] System

BioMed research international, 2022-04, Vol.2022 [Peer Reviewed Journal]

COPYRIGHT 2022 Hindawi Limited ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2022/7088063

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16
A review on chemical mechanism of microalgae flocculation via polymers
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A review on chemical mechanism of microalgae flocculation via polymers

Biotechnology reports (Amsterdam, Netherlands), 2019-03, Vol.21, p.e00302-e00302, Article e00302 [Peer Reviewed Journal]

2019 The Authors ;2019 The Authors 2019 ;ISSN: 2215-017X ;EISSN: 2215-017X ;DOI: 10.1016/j.btre.2018.e00302 ;PMID: 30671358

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17
Gold(I)-catalyzed intramolecular cyclization/intermolecular cycloaddition cascade as a fast track to polycarbocycles and mechanistic insights
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Gold(I)-catalyzed intramolecular cyclization/intermolecular cycloaddition cascade as a fast track to polycarbocycles and mechanistic insights

Nature communications, 2021-02, Vol.12 (1), p.1182-1182, Article 1182 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-21335-9 ;PMID: 33608521

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18
Synthesis of 4-aryl-3,4-dihydrocoumarins and 4-aryl-4H-chromenes via Er(OTf)3-catalyzed cascade reactions of p-quinone methides with 1,3-dicarbonyl compounds
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Synthesis of 4-aryl-3,4-dihydrocoumarins and 4-aryl-4H-chromenes via Er(OTf)3-catalyzed cascade reactions of p-quinone methides with 1,3-dicarbonyl compounds

RSC advances, 2023-05, Vol.13 (23), p.15942-15946 [Peer Reviewed Journal]

Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;EISSN: 2046-2069 ;DOI: 10.1039/d3ra02267f

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19
Divergent synthesis of N-heterocycles via controllable cyclization of azido-diynes catalyzed by copper and gold
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Divergent synthesis of N-heterocycles via controllable cyclization of azido-diynes catalyzed by copper and gold

Nature communications, 2017-11, Vol.8 (1), p.1748-9, Article 1748 [Peer Reviewed Journal]

2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2017 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-017-01853-1 ;PMID: 29170497

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20
Organocatalyst-mediated asymmetric one-pot/two domino/three-component coupling reactions for the synthesis of trans -hydrindanes
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Organocatalyst-mediated asymmetric one-pot/two domino/three-component coupling reactions for the synthesis of trans -hydrindanes

Chemical science (Cambridge), 2024-04, Vol.15 (15), p.5627-5632 [Peer Reviewed Journal]

This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2024 ;This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/d4sc00193a ;PMID: 38638214

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