22.1. 4.3 Dithiocarboxylic Acid Esters (Update 2024)
Book
Editors: Campagne, J.-M. ; Donohoe, T. J.; Fürstner, A. ; Jiang, X. ; Wang, M.
Title: Knowledge Updates 2024/1
Online ISBN: 9783132457058; Book DOI: 10.1055/b000000967
1st edition © 2024 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Laboratory Techniques, Stoichiometry;Organometallic Chemistry
Science of Synthesis Knowledge Updates
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: 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.
Type: Multivolume Edition
Abstract
Sulfur-containing functional groups feature widely in a broad spectrum of important compounds, including natural products, pharmaceuticals, and materials. Methods for the synthesis of dithiocarboxylic acid esters have been well-summarized and reviewed in Science of Synthesis in 2005; this update is focused on the most significant advances that have been reported since then.
Key words
dithiocarboxylic acid esters - thioacyl halides - thiocarboxylic acids - thiocarboxylic acid esters - carbon disulfide - Lawesson’s reagent - elemental sulfur - ynamides - Negishi cross coupling- 2 Petrova OV, Sagitova EF, Ushakov IA, Sobenina LN, Mikhaleva AI, Trofimov BA. J. Sulfur Chem. 2015; 36: 145
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- 4 Trofimov BA, Nedolya NA, Tarasova OA, Sobenina LN, Petrova OV, Sagitova EF, Albanov AI. J. Sulfur Chem. 2015; 36: 630
- 8 Malkov AV, Stewart-Liddon AJP, McGeoch GD, Ramírez-López P, Kočovský P. Org. Biomol. Chem. 2012; 10: 4864