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Heterocyclic Compounds
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Book
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Handbook of Heterocyclic Chemistry (3rd Edition)2010 ;ISBN: 0080958435 ;ISBN: 9780080958439 ;EISBN: 9780080958446 ;EISBN: 0080958443 ;DOI: 10.1016/C2009-0-05547-0 ;OCLC: 668210508Full text available |
| 2 |
Material Type: Article
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Recent advances in the synthesis of biologically and pharmaceutically active quinoline and its analogues: a reviewRSC advances, 2020-06, Vol.1 (35), p.2784-2793 [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: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d0ra03763j ;PMID: 35517753Full text available |
| 3 |
Material Type: Article
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Recent applications of Rose Bengal catalysis in N-heterocycles: a short reviewRSC advances, 2020-10, Vol.1 (65), p.39495-3958 [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: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d0ra07400d ;PMID: 35515398Full text available |
| 4 |
Material Type: Article
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Photochemical radical cyclization reactions with imines, hydrazones, oximes and related compoundsChemical Society reviews, 2021-07, Vol.50 (13), p.7418-7435 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0306-0012 ;EISSN: 1460-4744 ;DOI: 10.1039/D1CS00196EDigital Resources/Online E-Resources |
| 5 |
Material Type: Article
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2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug designRSC advances, 2018-01, Vol.8 (37), p.2894-2921 [Peer Reviewed Journal]This journal is © The Royal Society of Chemistry. ;This journal is © The Royal Society of Chemistry 2018 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/c8ra02827c ;PMID: 35542353Full text available |
| 6 |
Material Type: Article
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Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesteraseRSC advances, 2022-07, Vol.12 (31), p.19764-19855 [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/d2ra03081k ;PMID: 35919585Full text available |
| 7 |
Material Type: Article
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Recent developments and perspectives in the copper-catalyzed multicomponent synthesis of heterocyclesRSC advances, 2021-01, Vol.11 (6), p.3452-3469 [Peer Reviewed Journal]This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2021 ;This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d0ra10472h ;PMID: 35424324Full text available |
| 8 |
Material Type: Article
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Electrooxidation enables highly regioselective dearomative annulation of indole and benzofuran derivativesNature communications, 2020-01, Vol.11 (1), p.3-3, Article 3 [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/s41467-019-13829-4 ;PMID: 31911586Full text available |
| 9 |
Material Type: Article
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The ab-initio density matrix renormalization group in practiceThe Journal of chemical physics, 2015-01, Vol.142 (3), p.034102-034102 [Peer Reviewed Journal]ISSN: 0021-9606 ;EISSN: 1089-7690 ;DOI: 10.1063/1.4905329 ;PMID: 25612684Full text available |
| 10 |
Material Type: Article
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Heterocyclic Anticancer Compounds: Recent Advances and the Paradigm Shift towards the Use of Nanomedicine's Tool BoxMolecules, 2015-09, Vol.20 (9), p.16852-16891 [Peer Reviewed Journal]Copyright MDPI AG 2015 ;2015 by the authors. 2015 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules200916852 ;PMID: 26389876Full text available |
| 11 |
Material Type: Article
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A mini review of the synthesis of poly-1,2,3-triazole-based functional materialsRSC advances, 2017-01, Vol.7 (4), p.2281-2287 [Peer Reviewed Journal]Copyright Royal Society of Chemistry 2017 ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/c6ra27012cFull text available |
| 12 |
Material Type: Article
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Sustainable Mechanosynthesis of Biologically Active MoleculesEuropean journal of organic chemistry, 2022-06, Vol.2022 (21) [Peer Reviewed Journal]Attribution - NonCommercial - NoDerivatives ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202101516Digital Resources/Online E-Resources |
| 13 |
Material Type: Article
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Nitroketene N,S-acetals: synergistic building blocks for the synthesis of heterocyclesRSC advances, 2019-05, Vol.9 (25), p.14477-1452 [Peer Reviewed Journal]This journal is © The Royal Society of Chemistry. ;Copyright Royal Society of Chemistry 2019 ;This journal is © The Royal Society of Chemistry 2019 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/c9ra00630c ;PMID: 35519324Full text available |
| 14 |
Material Type: Article
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Synthesis of an aromatic N-heterocycle derived from biomass and its use as a polymer feedstockNature communications, 2019-05, Vol.10 (1), p.2107-2107, Article 2107 [Peer Reviewed Journal]The Author(s) 2019. 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) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-10178-0 ;PMID: 31068596Full text available |
| 15 |
Material Type: Article
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Time to Say Goodbye to the 16 EPA PAHs? Toward an Up-to-Date Use of PACs for Environmental PurposesPolycyclic aromatic compounds, 2015-03, Vol.35 (2-4), p.330-354 [Peer Reviewed Journal]2015 J. T. Andersson and C. Achten. Published with license by Taylor & Francis © J. T. Andersson and C. Achten 2015 ;ISSN: 1040-6638 ;EISSN: 1563-5333 ;DOI: 10.1080/10406638.2014.991042Digital Resources/Online E-Resources |
| 16 |
Material Type: Article
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Nickel-catalyzed oxidative C-H/N-H annulation of N -heteroaromatic compounds with alkynesChemical science (Cambridge), 2019-03, Vol.10 (11), p.3242-3248 [Peer Reviewed Journal]Copyright Royal Society of Chemistry 2019 ;ISSN: 2041-6520 ;EISSN: 2041-6539 ;DOI: 10.1039/c8sc05063e ;PMID: 30996908Full text available |
| 17 |
Material Type: Article
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Oxidative Carbonylation as a Powerful Tool for the Direct Synthesis of Carbonylated HeterocyclesEuropean journal of organic chemistry, 2012-12, Vol.2012 (35), p.6825-6839 [Peer Reviewed Journal]Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2014 INIST-CNRS ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.201200794Full text available |
| 18 |
Material Type: Article
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Unravelling the synthetic and therapeutic aspects of five, six and fused heterocycles using Vilsmeier-Haack reagentRSC advances, 2023-09, Vol.13 (38), p.2664-26629 [Peer Reviewed Journal]Copyright Royal Society of Chemistry 2023 ;This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry ;ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/d3ra04309fFull text available |
| 19 |
Material Type: Article
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Isatin and its derivatives: a survey of recent syntheses, reactions, and applicationsMedChemComm, 2019-03, Vol.1 (3), p.351-368 [Peer Reviewed Journal]Copyright Royal Society of Chemistry 2019 ;This journal is © The Royal Society of Chemistry 2019 2019 ;ISSN: 2040-2503 ;EISSN: 2040-2511 ;DOI: 10.1039/c8md00585k ;PMID: 30996856Full text available |
| 20 |
Material Type: Book
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N-Heterocyclic Carbenes in Transition Metal Catalysis and OrganocatalysisSpringer Science+Business Media B.V. 2011 ;ISSN: 0920-4652 ;ISBN: 9048128668 ;ISBN: 9789048128662 ;ISBN: 904812865X ;ISBN: 9789048128655 ;EISBN: 9048128668 ;EISBN: 9789048128662 ;DOI: 10.1007/978-90-481-2866-2 ;OCLC: 704395339Full text available |
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