Synthesis of Heteroaromatic Compounds
This Special Issue, entitled the “Synthesis of Heteroaromatic Compounds”, is an outstanding collection of fourteen original research papers and six review articles that discuss the advances made in both conventional and green preparatory methods, as well as the properties and applications of heteroa...
Uloženo v:
| Médium: | Online |
|---|---|
| Jazyk: | angličtina |
| Vydáno: |
MDPI - Multidisciplinary Digital Publishing Institute
2023
|
| Témata: | |
| On-line přístup: | ONIX_20230623_9783036575636_45 |
| Tagy: |
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
|
| _version_ | 1869527500564987904 |
|---|---|
| collection | Directory of Open Access Books |
| description | This Special Issue, entitled the “Synthesis of Heteroaromatic Compounds”, is an outstanding collection of fourteen original research papers and six review articles that discuss the advances made in both conventional and green preparatory methods, as well as the properties and applications of heteroaromatic molecules in industrial and medicinal chemistry areas of study.The collected works featured herein collate contributions from a truly international and diverse array of ninety experts in the fields of heteroaromatic compound synthesis, QSAR studies, computational chemistry and molecular docking, as well as bioactivity studies. |
| format | Online |
| id | doab-20.500.12854ir-100813 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2023 |
| publishDateRange | 2023 |
| publishDateSort | 2023 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-1008132024-03-28T03:33:07Z Synthesis of Heteroaromatic Compounds Sloop, Joseph heteroaromatics C-H bond functionalization oxidative cyclization cross-coupling amination triazoles palladium carbene ligands heterocycles nitrogen-containing heterocycles synthesis antiviral agents viruses COVID-19 inhibition Mpro inhibitors drug design and synthesis structure-activity relationships (SAR) s-tetrazine 4H-1,2,4-triazole pinner reaction 1,2,3-triazole fused 1,2,3-triazole 1,2,3-triazolo[4,5-b]pyrazine 1,2,3-triazolo[4,5-c]pyridazine 1,2,3-triazolo[4,5-d]pyridazine 1,2,3-triazolo[1,5-a]pyrazine 1,2,3-triazolo[1,5-b]pyridazine triazolopyrazine triazolopyridazine practical applications spiro π-conjugated compound chiral compound thiophene furan pyrrole nucleophilic aromatic substitution circular dichroism circularly polarized luminescence pyridines 1,3,4-thiadiazoles 1,3-thiazoles hydrazonoyl halides molecular docking anticancer activity 1,3,4-oxadiazoles organic ligands substitution diisopropyl iminodiacetate pyrimidine benzimidazole aza-Diels–Alder reaction Povarov reaction oxidation fluorescence aggregation-induced emission mechanochromic properties heterocycle natural product nicotinic acid fungicidal activity 4-pyrone DMF-DMA enamination cycloaddition merocyanine 1,6-conjugate addition solvatochromism fluorophore acetylcoumarin thiazoles VEGFR-2 polyfluoroflavones 1H-1,2,4-triazole imidazole regioselectivity azolyl-substituted flavones photoluminescence 4-pyridone oxazinone ring-opening aldehyde-lactol tautomerism ammonium acetate diazirine medicinal chemistry photoaffinity labeling metathesis carboaromatics 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines novel scaffold molecular dynamic studies proximity frequencies (PF) GABAA receptor subtype GABAA receptor ligands antibacterial anticancer antifibrotic antifungal antimicrobial antiviral appel salt 1,2,3-dithiazole disulfide bridge herbicidal chalcone heteroaromatic hybrid chalcone n/a thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PN Chemistry thema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistry This Special Issue, entitled the “Synthesis of Heteroaromatic Compounds”, is an outstanding collection of fourteen original research papers and six review articles that discuss the advances made in both conventional and green preparatory methods, as well as the properties and applications of heteroaromatic molecules in industrial and medicinal chemistry areas of study.The collected works featured herein collate contributions from a truly international and diverse array of ninety experts in the fields of heteroaromatic compound synthesis, QSAR studies, computational chemistry and molecular docking, as well as bioactivity studies. 2023-06-23T09:44:45Z 2023-06-23T09:44:45Z 2023 book ONIX_20230623_9783036575636_45 9783036575636 9783036575629 https://directory.doabooks.org/handle/20.500.12854/100813 eng image/jpeg Attribution 4.0 International https://mdpi.com/books/pdfview/book/7276 https://mdpi.com/books/pdfview/book/7276 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-7562-9 10.3390/books978-3-0365-7562-9 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036575636 9783036575629 446 Basel open access |
| spellingShingle | heteroaromatics C-H bond functionalization oxidative cyclization cross-coupling amination triazoles palladium carbene ligands heterocycles nitrogen-containing heterocycles synthesis antiviral agents viruses COVID-19 inhibition Mpro inhibitors drug design and synthesis structure-activity relationships (SAR) s-tetrazine 4H-1,2,4-triazole pinner reaction 1,2,3-triazole fused 1,2,3-triazole 1,2,3-triazolo[4,5-b]pyrazine 1,2,3-triazolo[4,5-c]pyridazine 1,2,3-triazolo[4,5-d]pyridazine 1,2,3-triazolo[1,5-a]pyrazine 1,2,3-triazolo[1,5-b]pyridazine triazolopyrazine triazolopyridazine practical applications spiro π-conjugated compound chiral compound thiophene furan pyrrole nucleophilic aromatic substitution circular dichroism circularly polarized luminescence pyridines 1,3,4-thiadiazoles 1,3-thiazoles hydrazonoyl halides molecular docking anticancer activity 1,3,4-oxadiazoles organic ligands substitution diisopropyl iminodiacetate pyrimidine benzimidazole aza-Diels–Alder reaction Povarov reaction oxidation fluorescence aggregation-induced emission mechanochromic properties heterocycle natural product nicotinic acid fungicidal activity 4-pyrone DMF-DMA enamination cycloaddition merocyanine 1,6-conjugate addition solvatochromism fluorophore acetylcoumarin thiazoles VEGFR-2 polyfluoroflavones 1H-1,2,4-triazole imidazole regioselectivity azolyl-substituted flavones photoluminescence 4-pyridone oxazinone ring-opening aldehyde-lactol tautomerism ammonium acetate diazirine medicinal chemistry photoaffinity labeling metathesis carboaromatics 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines novel scaffold molecular dynamic studies proximity frequencies (PF) GABAA receptor subtype GABAA receptor ligands antibacterial anticancer antifibrotic antifungal antimicrobial antiviral appel salt 1,2,3-dithiazole disulfide bridge herbicidal chalcone heteroaromatic hybrid chalcone n/a thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PN Chemistry thema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistry Synthesis of Heteroaromatic Compounds |
| title | Synthesis of Heteroaromatic Compounds |
| title_full | Synthesis of Heteroaromatic Compounds |
| title_fullStr | Synthesis of Heteroaromatic Compounds |
| title_full_unstemmed | Synthesis of Heteroaromatic Compounds |
| title_short | Synthesis of Heteroaromatic Compounds |
| title_sort | synthesis of heteroaromatic compounds |
| topic | heteroaromatics C-H bond functionalization oxidative cyclization cross-coupling amination triazoles palladium carbene ligands heterocycles nitrogen-containing heterocycles synthesis antiviral agents viruses COVID-19 inhibition Mpro inhibitors drug design and synthesis structure-activity relationships (SAR) s-tetrazine 4H-1,2,4-triazole pinner reaction 1,2,3-triazole fused 1,2,3-triazole 1,2,3-triazolo[4,5-b]pyrazine 1,2,3-triazolo[4,5-c]pyridazine 1,2,3-triazolo[4,5-d]pyridazine 1,2,3-triazolo[1,5-a]pyrazine 1,2,3-triazolo[1,5-b]pyridazine triazolopyrazine triazolopyridazine practical applications spiro π-conjugated compound chiral compound thiophene furan pyrrole nucleophilic aromatic substitution circular dichroism circularly polarized luminescence pyridines 1,3,4-thiadiazoles 1,3-thiazoles hydrazonoyl halides molecular docking anticancer activity 1,3,4-oxadiazoles organic ligands substitution diisopropyl iminodiacetate pyrimidine benzimidazole aza-Diels–Alder reaction Povarov reaction oxidation fluorescence aggregation-induced emission mechanochromic properties heterocycle natural product nicotinic acid fungicidal activity 4-pyrone DMF-DMA enamination cycloaddition merocyanine 1,6-conjugate addition solvatochromism fluorophore acetylcoumarin thiazoles VEGFR-2 polyfluoroflavones 1H-1,2,4-triazole imidazole regioselectivity azolyl-substituted flavones photoluminescence 4-pyridone oxazinone ring-opening aldehyde-lactol tautomerism ammonium acetate diazirine medicinal chemistry photoaffinity labeling metathesis carboaromatics 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines novel scaffold molecular dynamic studies proximity frequencies (PF) GABAA receptor subtype GABAA receptor ligands antibacterial anticancer antifibrotic antifungal antimicrobial antiviral appel salt 1,2,3-dithiazole disulfide bridge herbicidal chalcone heteroaromatic hybrid chalcone n/a thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PN Chemistry thema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistry |
| topic_facet | heteroaromatics C-H bond functionalization oxidative cyclization cross-coupling amination triazoles palladium carbene ligands heterocycles nitrogen-containing heterocycles synthesis antiviral agents viruses COVID-19 inhibition Mpro inhibitors drug design and synthesis structure-activity relationships (SAR) s-tetrazine 4H-1,2,4-triazole pinner reaction 1,2,3-triazole fused 1,2,3-triazole 1,2,3-triazolo[4,5-b]pyrazine 1,2,3-triazolo[4,5-c]pyridazine 1,2,3-triazolo[4,5-d]pyridazine 1,2,3-triazolo[1,5-a]pyrazine 1,2,3-triazolo[1,5-b]pyridazine triazolopyrazine triazolopyridazine practical applications spiro π-conjugated compound chiral compound thiophene furan pyrrole nucleophilic aromatic substitution circular dichroism circularly polarized luminescence pyridines 1,3,4-thiadiazoles 1,3-thiazoles hydrazonoyl halides molecular docking anticancer activity 1,3,4-oxadiazoles organic ligands substitution diisopropyl iminodiacetate pyrimidine benzimidazole aza-Diels–Alder reaction Povarov reaction oxidation fluorescence aggregation-induced emission mechanochromic properties heterocycle natural product nicotinic acid fungicidal activity 4-pyrone DMF-DMA enamination cycloaddition merocyanine 1,6-conjugate addition solvatochromism fluorophore acetylcoumarin thiazoles VEGFR-2 polyfluoroflavones 1H-1,2,4-triazole imidazole regioselectivity azolyl-substituted flavones photoluminescence 4-pyridone oxazinone ring-opening aldehyde-lactol tautomerism ammonium acetate diazirine medicinal chemistry photoaffinity labeling metathesis carboaromatics 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines novel scaffold molecular dynamic studies proximity frequencies (PF) GABAA receptor subtype GABAA receptor ligands antibacterial anticancer antifibrotic antifungal antimicrobial antiviral appel salt 1,2,3-dithiazole disulfide bridge herbicidal chalcone heteroaromatic hybrid chalcone n/a thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PN Chemistry thema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistry |
| url | ONIX_20230623_9783036575636_45 |