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 fac...
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Format: | Electronic Book Chapter |
Language: | English |
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Basel
MDPI - Multidisciplinary Digital Publishing Institute
2023
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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100 | 1 | |a Darabantu, Mircea |4 edt | |
700 | 1 | |a Rinderspacher, Alison |4 edt | |
700 | 1 | |a Proni, Gloria |4 edt | |
700 | 1 | |a Darabantu, Mircea |4 oth | |
700 | 1 | |a Rinderspacher, Alison |4 oth | |
700 | 1 | |a Proni, Gloria |4 oth | |
245 | 1 | 0 | |a New Approaches to Synthetic Organic Chemistry |
260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2023 | ||
300 | |a 1 electronic resource (182 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a 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. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Research & information: general |2 bicssc | |
650 | 7 | |a Chemistry |2 bicssc | |
650 | 7 | |a Organic chemistry |2 bicssc | |
653 | |a 3-(1,3-diarylallylidene)oxindole | ||
653 | |a knoevenagel condensation | ||
653 | |a allylic oxidation | ||
653 | |a wittig reaction | ||
653 | |a aldol reaction | ||
653 | |a non-palladium-catalyzed | ||
653 | |a glycals | ||
653 | |a 2-OH thioglycosides | ||
653 | |a glycosyl donors | ||
653 | |a glycosylation | ||
653 | |a one-pot reaction | ||
653 | |a cyclopropenes | ||
653 | |a cyclopropanes | ||
653 | |a nucleophilic addition | ||
653 | |a metal-templated reactions | ||
653 | |a flavonoids | ||
653 | |a 1,3-dithiolium salts | ||
653 | |a dithiocarbamates | ||
653 | |a homophthalic anhydride | ||
653 | |a imine | ||
653 | |a Castagnoli-Cushman reaction | ||
653 | |a tetrahydroisoquinolone | ||
653 | |a lactam | ||
653 | |a all-carbon quaternary atom | ||
653 | |a gold(I)-catalyzed | ||
653 | |a arylalkyne | ||
653 | |a benzene derivatives | ||
653 | |a cyclopentene derivatives | ||
653 | |a furan and pyran derivatives | ||
653 | |a copper catalysis | ||
653 | |a asymmetric reaction | ||
653 | |a desymmetrization | ||
653 | |a glycerol | ||
653 | |a polycyclic aromatic hydrocarbon | ||
653 | |a double hetero[7]helicene | ||
653 | |a short-step synthesis | ||
653 | |a electrochemical cross-coupling | ||
653 | |a nucleus-independent chemical shift | ||
653 | |a acylethynylpyrroles | ||
653 | |a alkynones | ||
653 | |a terminal alkynes | ||
653 | |a deacylation | ||
653 | |a retro-Favorsky reaction | ||
653 | |a asymmetric organocatalysis | ||
653 | |a quaternary ammonium salts | ||
653 | |a phase-transfer catalysts (PTCs) | ||
653 | |a camphor | ||
653 | |a camphor-derived diamines | ||
653 | |a β-keto esters | ||
653 | |a enantioselective α-fluorination | ||
653 | |a electrophilic α-chlorination | ||
653 | |a asymmetric Michael addition | ||
653 | |a α-nitroketones | ||
653 | |a alkenes | ||
653 | |a alkynes | ||
653 | |a 1,3-dipolar cycloaddition | ||
653 | |a p-TsOH | ||
653 | |a isoxazolines | ||
653 | |a nitroacrylates | ||
653 | |a organocatalysis | ||
653 | |a stereoselective synthesis | ||
653 | |a reduction | ||
653 | |a chiral nitro derivatives | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/8025 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/128573 |7 0 |z DOAB: description of the publication |