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Journal Of The American Chemical Society
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
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Electronic Decoupling in C3-Symmetrical Light-Responsive Tris(Azobenzene) Scaffolds: Self-Assembly and MultiphotochromismJournal of the American Chemical Society, 2018-11, Vol.140 (47), p.16062-16070 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b06324Digital Resources/Online E-Resources |
| 2 |
Material Type: Article
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Photochemical Ring-Opening Reaction of 1,3-Cyclohexadiene: Identifying the True Reactive StateJournal of the American Chemical Society, 2022-12, Vol.144 (48), p.21878-21886 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.2c06296Digital Resources/Online E-Resources |
| 3 |
Material Type: Article
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Axially and Helically Chiral Cationic Radical Bicarbazoles: SOMO-HOMO Level Inversion and Chirality Impact on the Sta- bility of Mono-and Diradical CationsJournal of the American Chemical Society, 2020-11, Vol.142 (48), p.20409-20418 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.0c08948 ;PMID: 33201694Digital Resources/Online E-Resources |
| 4 |
Material Type: Article
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Selectively photocatalytic dehydrogenation of formic acid by in-situ restructured copper post-metalated metal organic framework under visible lightJournal of the American Chemical Society, 2022, Vol.144 (36), p.16433-16446 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.2c04905Digital Resources/Online E-Resources |
| 5 |
Material Type: Article
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Dynamic Carbon Isotope Exchange of Pharmaceuticals with Labeled CO$_2Journal of the American Chemical Society, 2019-01, Vol.141 (2), p.780-784 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b12140Digital Resources/Online E-Resources |
| 6 |
Material Type: Article
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Sydnone-based Approach to Hetero-helicenes Through 1,3-Dipolar-CycloadditionsJournal of the American Chemical Society, 2019-01, Vol.141, p.1435-1440 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b11465Digital Resources/Online E-Resources |
| 7 |
Material Type: Article
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Lemniscular [16]Cycloparaphenylene A Radially Conjugated Figure-Eight Aromatic MoleculeJournal of the American Chemical Society, 2019-05, Vol.141 (18), p.7421-7427 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.9b01797 ;PMID: 30998349Digital Resources/Online E-Resources |
| 8 |
Material Type: Article
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Covalent Adaptable Networks Using β-Amino Esters as Thermally Reversible Building BlocksJournal of the American Chemical Society, 2021-06, Vol.143 (24), p.9140-9150 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.1c03316Digital Resources/Online E-Resources |
| 9 |
Material Type: Article
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Chiral Nanographene Propeller Embedding Six Enantiomerically Stable [5]Helicene UnitsJournal of the American Chemical Society, 2017-12, Vol.139 (51), p.18508-18511 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.7b07622Digital Resources/Online E-Resources |
| 10 |
Material Type: Article
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What Are the Radical Intermediates in Oxidative N -Heterocyclic Carbene Organocatalysis?Journal of the American Chemical Society, 2019-01, Vol.141 (2), p.1109-1117 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b11824Digital Resources/Online E-Resources |
| 11 |
Material Type: Article
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Chemically Fueled Three-State Chiroptical Switching Supramolecular Gel with Temporal ControlJournal of the American Chemical Society, 2021-08, Vol.143 (32), p.12650-12657 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.1c05183Digital Resources/Online E-Resources |
| 12 |
Material Type: Article
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Ligand-Controlled Regiodivergent Palladium-Catalyzed Hydrogermylation of YnamidesJournal of the American Chemical Society, 2020-06, Vol.142 (25) [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.0c03556Digital Resources/Online E-Resources |
| 13 |
Material Type: Article
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Reductive Coupling of Nitroarenes and HCHO for General Synthesis of Functional Ethane-1,2-diamines by a Cobalt Single-Atom CatalystJournal of the American Chemical Society, 2023-08, Vol.145 (31) [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.3c04857 ;PMID: 37418675Digital Resources/Online E-Resources |
| 14 |
Material Type: Article
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Radical Germylzincation of α-Heteroatom-Substituted AlkynesJournal of the American Chemical Society, 2018-12, Vol.140 (50), p.17632-17642 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b09851Digital Resources/Online E-Resources |
| 15 |
Material Type: Article
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Targeted solvatochromic fluorescent probes for imaging lipid order in organelles under oxidative and mechanical stressJournal of the American Chemical Society, 2021-01, Vol.143 (2), p.912-924 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.0c10972Digital Resources/Online E-Resources |
| 16 |
Material Type: Article
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Urea-Based Imprinted Polymer Hosts with Switchable Anion PreferenceJournal of the American Chemical Society, 2020-07, Vol.142 (26), p.11404 [Peer Reviewed Journal]ISSN: 1520-5126 ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.0c00707Digital Resources/Online E-Resources |
| 17 |
Material Type: Article
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Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion StrategyJournal of the American Chemical Society, 2017-02, Vol.139 (6), p.2140-2143 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.6b11079Digital Resources/Online E-Resources |
| 18 |
Material Type: Article
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Enantioselective and Diastereodivergent Synthesis of Spiroindolenines via Chiral Phosphoric Acid-Catalyzed CycloadditionJournal of the American Chemical Society, 2021-08, Vol.143 (30), p.11611-11619 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.1c04648Digital Resources/Online E-Resources |
| 19 |
Material Type: Article
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Merging C-H Bond Activation, Alkyne Insertion, and Rearrangements by Rh(III)-Catalysis: Oxindole Synthesis from Nitroarenes and AlkynesJournal of the American Chemical Society, 2023-03, Vol.145 (8) [Peer Reviewed Journal]Attribution ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.2c10932 ;PMID: 36802602Digital Resources/Online E-Resources |
| 20 |
Material Type: Article
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Synthesis of Cyclopentenones with C4-Quaternary Stereocenters via Stereospecific [3,3]-Sigmatropic Rearrangement and Applications in Total Synthesis of SesquiterpenoidsJournal of the American Chemical Society, 2021-10 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.1c07966Digital Resources/Online E-Resources |
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