Modern Strategies for Heterocycle Synthesis
Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-couplin...
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| Jezik: | angleščina |
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MDPI - Multidisciplinary Digital Publishing Institute
2021
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| Online dostop: | ONIX_20210501_9783036503400_233 |
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| _version_ | 1869518183588691968 |
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| collection | Directory of Open Access Books |
| description | Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome. |
| format | Online |
| id | doab-20.500.12854ir-68487 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2021 |
| publishDateRange | 2021 |
| publishDateSort | 2021 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-684872024-03-30T23:22:15Z Modern Strategies for Heterocycle Synthesis Favi, Gianfranco amine nucleophiles alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2′:6′,3″-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure–activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach n/a thema EDItEUR::M Medicine and Nursing Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome. 2021-05-01T15:11:12Z 2021-05-01T15:11:12Z 2021 book ONIX_20210501_9783036503400_233 9783036503400 9783036503417 https://directory.doabooks.org/handle/20.500.12854/68487 eng application/octet-stream Attribution 4.0 International https://mdpi.com/books/pdfview/book/3507 https://mdpi.com/books/pdfview/book/3507 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-0341-7 10.3390/books978-3-0365-0341-7 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036503400 9783036503417 372 Basel, Switzerland open access |
| spellingShingle | amine nucleophiles alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2′:6′,3″-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure–activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach n/a thema EDItEUR::M Medicine and Nursing Modern Strategies for Heterocycle Synthesis |
| title | Modern Strategies for Heterocycle Synthesis |
| title_full | Modern Strategies for Heterocycle Synthesis |
| title_fullStr | Modern Strategies for Heterocycle Synthesis |
| title_full_unstemmed | Modern Strategies for Heterocycle Synthesis |
| title_short | Modern Strategies for Heterocycle Synthesis |
| title_sort | modern strategies for heterocycle synthesis |
| topic | amine nucleophiles alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2′:6′,3″-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure–activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach n/a thema EDItEUR::M Medicine and Nursing |
| topic_facet | amine nucleophiles alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2′:6′,3″-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure–activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach n/a thema EDItEUR::M Medicine and Nursing |
| url | ONIX_20210501_9783036503400_233 |