New Approaches to Synthetic Organic Chemistry
The "New Approaches to Synthetic Organic Chemistry" Special Issue has continued to challenge and expand our scientific knowledge of the surrounding world, exploring the frontiers between at least two of its dynamic interfaces: human life and the environment. Subject to all evolutionary facets of org...
Sparad:
| Materialtyp: | Online |
|---|---|
| Språk: | engelska |
| Utgiven: |
MDPI - Multidisciplinary Digital Publishing Institute
2023
|
| Ämnen: | |
| Länkar: | ONIX_20231130_9783036590202_25 |
| Taggar: |
Inga taggar, Lägg till första taggen!
|
| _version_ | 1869526093940129792 |
|---|---|
| collection | Directory of Open Access Books |
| description | The "New Approaches to Synthetic Organic Chemistry" Special Issue has continued to challenge and expand our scientific knowledge of the surrounding world, exploring the frontiers between at least two of its dynamic interfaces: human life and the environment. Subject to all evolutionary facets of organic chemistry, its perpetual developments reimagined within the current organic synthesis (strategies, methodologies, reaction mechanisms, reagents, catalysts, chemical and instrumental auxiliaries) nevertheless obey two crucial common denominators, "selectivity" vs. “specificity” (these terms being, equally, preceded by typical prefixes, either chemo-, regio- or stereo-), as mandatory criteria. The present Special Issue gathered research articles, communications, and review papers, disclosing the most recent advances in organic synthesis, i.e., those related to its near future defined as “atomic precision” in chemical reactions. The sustainability of these efforts, which denotes an intrinsic chemical diversity, is expected to highlight, to the interested readers, their innovative applications in human life and the environment. |
| format | Online |
| id | doab-20.500.12854ir-128573 |
| 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-1285732024-03-28T03:33:06Z New Approaches to Synthetic Organic Chemistry Darabantu, Mircea Rinderspacher, Alison Proni, Gloria 3-(1,3-diarylallylidene)oxindole knoevenagel condensation allylic oxidation wittig reaction aldol reaction non-palladium-catalyzed glycals 2-OH thioglycosides glycosyl donors glycosylation one-pot reaction cyclopropenes cyclopropanes nucleophilic addition metal-templated reactions flavonoids 1,3-dithiolium salts dithiocarbamates homophthalic anhydride imine Castagnoli–Cushman reaction tetrahydroisoquinolone lactam all-carbon quaternary atom gold(I)-catalyzed arylalkyne benzene derivatives cyclopentene derivatives furan and pyran derivatives copper catalysis asymmetric reaction desymmetrization glycerol polycyclic aromatic hydrocarbon double hetero[7]helicene short-step synthesis electrochemical cross-coupling nucleus-independent chemical shift acylethynylpyrroles alkynones terminal alkynes deacylation retro-Favorsky reaction asymmetric organocatalysis quaternary ammonium salts phase-transfer catalysts (PTCs) camphor camphor-derived diamines β-keto esters enantioselective α-fluorination electrophilic α-chlorination asymmetric Michael addition α-nitroketones alkenes alkynes 1,3-dipolar cycloaddition p-TsOH isoxazolines nitroacrylates organocatalysis stereoselective synthesis reduction chiral nitro derivatives 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 The "New Approaches to Synthetic Organic Chemistry" Special Issue has continued to challenge and expand our scientific knowledge of the surrounding world, exploring the frontiers between at least two of its dynamic interfaces: human life and the environment. Subject to all evolutionary facets of organic chemistry, its perpetual developments reimagined within the current organic synthesis (strategies, methodologies, reaction mechanisms, reagents, catalysts, chemical and instrumental auxiliaries) nevertheless obey two crucial common denominators, "selectivity" vs. “specificity” (these terms being, equally, preceded by typical prefixes, either chemo-, regio- or stereo-), as mandatory criteria. The present Special Issue gathered research articles, communications, and review papers, disclosing the most recent advances in organic synthesis, i.e., those related to its near future defined as “atomic precision” in chemical reactions. The sustainability of these efforts, which denotes an intrinsic chemical diversity, is expected to highlight, to the interested readers, their innovative applications in human life and the environment. 2023-11-30T20:32:46Z 2023-11-30T20:32:46Z 2023 book ONIX_20231130_9783036590202_25 9783036590202 9783036590219 https://directory.doabooks.org/handle/20.500.12854/128573 eng application/octet-stream Attribution 4.0 International https://mdpi.com/books/pdfview/book/8025 https://mdpi.com/books/pdfview/book/8025 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-9021-9 10.3390/books978-3-0365-9021-9 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036590202 9783036590219 182 Basel open access |
| spellingShingle | 3-(1,3-diarylallylidene)oxindole knoevenagel condensation allylic oxidation wittig reaction aldol reaction non-palladium-catalyzed glycals 2-OH thioglycosides glycosyl donors glycosylation one-pot reaction cyclopropenes cyclopropanes nucleophilic addition metal-templated reactions flavonoids 1,3-dithiolium salts dithiocarbamates homophthalic anhydride imine Castagnoli–Cushman reaction tetrahydroisoquinolone lactam all-carbon quaternary atom gold(I)-catalyzed arylalkyne benzene derivatives cyclopentene derivatives furan and pyran derivatives copper catalysis asymmetric reaction desymmetrization glycerol polycyclic aromatic hydrocarbon double hetero[7]helicene short-step synthesis electrochemical cross-coupling nucleus-independent chemical shift acylethynylpyrroles alkynones terminal alkynes deacylation retro-Favorsky reaction asymmetric organocatalysis quaternary ammonium salts phase-transfer catalysts (PTCs) camphor camphor-derived diamines β-keto esters enantioselective α-fluorination electrophilic α-chlorination asymmetric Michael addition α-nitroketones alkenes alkynes 1,3-dipolar cycloaddition p-TsOH isoxazolines nitroacrylates organocatalysis stereoselective synthesis reduction chiral nitro derivatives 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 New Approaches to Synthetic Organic Chemistry |
| title | New Approaches to Synthetic Organic Chemistry |
| title_full | New Approaches to Synthetic Organic Chemistry |
| title_fullStr | New Approaches to Synthetic Organic Chemistry |
| title_full_unstemmed | New Approaches to Synthetic Organic Chemistry |
| title_short | New Approaches to Synthetic Organic Chemistry |
| title_sort | new approaches to synthetic organic chemistry |
| topic | 3-(1,3-diarylallylidene)oxindole knoevenagel condensation allylic oxidation wittig reaction aldol reaction non-palladium-catalyzed glycals 2-OH thioglycosides glycosyl donors glycosylation one-pot reaction cyclopropenes cyclopropanes nucleophilic addition metal-templated reactions flavonoids 1,3-dithiolium salts dithiocarbamates homophthalic anhydride imine Castagnoli–Cushman reaction tetrahydroisoquinolone lactam all-carbon quaternary atom gold(I)-catalyzed arylalkyne benzene derivatives cyclopentene derivatives furan and pyran derivatives copper catalysis asymmetric reaction desymmetrization glycerol polycyclic aromatic hydrocarbon double hetero[7]helicene short-step synthesis electrochemical cross-coupling nucleus-independent chemical shift acylethynylpyrroles alkynones terminal alkynes deacylation retro-Favorsky reaction asymmetric organocatalysis quaternary ammonium salts phase-transfer catalysts (PTCs) camphor camphor-derived diamines β-keto esters enantioselective α-fluorination electrophilic α-chlorination asymmetric Michael addition α-nitroketones alkenes alkynes 1,3-dipolar cycloaddition p-TsOH isoxazolines nitroacrylates organocatalysis stereoselective synthesis reduction chiral nitro derivatives 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 | 3-(1,3-diarylallylidene)oxindole knoevenagel condensation allylic oxidation wittig reaction aldol reaction non-palladium-catalyzed glycals 2-OH thioglycosides glycosyl donors glycosylation one-pot reaction cyclopropenes cyclopropanes nucleophilic addition metal-templated reactions flavonoids 1,3-dithiolium salts dithiocarbamates homophthalic anhydride imine Castagnoli–Cushman reaction tetrahydroisoquinolone lactam all-carbon quaternary atom gold(I)-catalyzed arylalkyne benzene derivatives cyclopentene derivatives furan and pyran derivatives copper catalysis asymmetric reaction desymmetrization glycerol polycyclic aromatic hydrocarbon double hetero[7]helicene short-step synthesis electrochemical cross-coupling nucleus-independent chemical shift acylethynylpyrroles alkynones terminal alkynes deacylation retro-Favorsky reaction asymmetric organocatalysis quaternary ammonium salts phase-transfer catalysts (PTCs) camphor camphor-derived diamines β-keto esters enantioselective α-fluorination electrophilic α-chlorination asymmetric Michael addition α-nitroketones alkenes alkynes 1,3-dipolar cycloaddition p-TsOH isoxazolines nitroacrylates organocatalysis stereoselective synthesis reduction chiral nitro derivatives 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_20231130_9783036590202_25 |