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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Other Authors: Darabantu, Mircea (Editor), Rinderspacher, Alison (Editor), Proni, Gloria (Editor)
Format: Electronic Book Chapter
Language:English
Published: 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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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. 
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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 
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