33.1. 8.2 Alk-1-enyl Sulfides (Update 2024)
Buch
Herausgeber: Campagne, J.-M. ; Donohoe, T. J.; Drabowicz, J. ; Fuerstner, A. ; Jiang, X. ; Wang, M. ; Wirth, T.
Titel: Knowledge Updates 2024/3
Online ISBN: 9783132457089; Buch-DOI: 10.1055/b000000969
1st edition © 2024 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Knowledge Updates
Übergeordnete Publikation
Titel: Science of Synthesis
DOI: 10.1055/b-00000101
Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Typ: Mehrbändiges Werk
Abstract
Alk-1-enyl sulfides are an interesting class of compounds that are widely used in organic synthesis. There are a large variety of methods for their preparation, employing both substrates and reagents as the sulfur source. Most recent advances (in the period 2006–2022) reported for the synthesis of alk-1-enyl sulfides have involved the preparation of variously substituted derivatives of the title compounds. The substituents include halogens (fluorine and polyfluoroalkyls, chlorine, bromine, and iodine), the nitro group, and acyloxy, ester, carboxy, sulfonyl, and amino groups. The application of various sulfur sources and synthetic strategies to form alk-1-enyl sulfides, and finally the synthesis of cyclic alk-1-enyl sulfides and polyene alk-1-enyl sulfides are also reported.
Schlüsselwörter
alkenyl sulfides - polyenyl sulfides - alkenes - alkynes - sulfanylation of alkynes - perhalogenoalkenes - thiols - palladium catalysis - copper catalysis - gold catalysis - ruthenium catalysis - dithioesters - carbon disulfide - isothiocyanates - sulfonothioates - β-sulfinyl esters - thiirenium ions - electrochemical cross-coupling reactions-
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