Reprint

New Approaches to Synthetic Organic Chemistry

Edited by
October 2023
182 pages
  • ISBN978-3-0365-9020-2 (Hardback)
  • ISBN978-3-0365-9021-9 (PDF)

This book is a reprint of the Special Issue New Approaches to Synthetic Organic Chemistry that was published in

Chemistry & Materials Science
Medicine & Pharmacology
Summary

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
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
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