Asymmetric synthesis with ynamides: unique reaction control, chemical diversity and applications
Ynamides are among the most powerful building blocks in organic synthesis and have
become invaluable starting materials for the construction of multifunctional compounds and …
become invaluable starting materials for the construction of multifunctional compounds and …
Ynamides in free radical reactions
C Mahe, K Cariou - Advanced Synthesis & Catalysis, 2020 - Wiley Online Library
In this review we present the transformations that have been developed with ynamides and
free radicals. These reactions involve carbon‐, heteroatom‐or even metalloid‐centered …
free radicals. These reactions involve carbon‐, heteroatom‐or even metalloid‐centered …
Ketenimines Generated from Ynamides: Versatile Building Blocks for Nitrogen‐Containing Scaffolds
RH Dodd, K Cariou - Chemistry–A European Journal, 2018 - Wiley Online Library
Using ynamides as readily available starting materials, a single step can generate highly
reactive ketenimines, which can then undergo a variety of transformations. The choice of the …
reactive ketenimines, which can then undergo a variety of transformations. The choice of the …
Carboxylation Reactions with Carbon Dioxide Using N‐Heterocyclic Carbene‐Copper Catalysts
L Zhang, Z Li, M Takimoto, Z Hou - The Chemical Record, 2020 - Wiley Online Library
The development of versatile catalyst systems and new transformations for the utilization of
carbon dioxide (CO2) is of great interest and significance. This Personal Account reviews …
carbon dioxide (CO2) is of great interest and significance. This Personal Account reviews …
Ligand-controlled regiodivergent palladium-catalyzed hydrogermylation of ynamides
V Debrauwer, A Turlik, L Rummler… - Journal of the …, 2020 - ACS Publications
Ynamides are fascinating small molecules with complementary reactivities under radical,
ionic, and metal-catalyzed conditions. We report herein synthetic and DFT investigations of …
ionic, and metal-catalyzed conditions. We report herein synthetic and DFT investigations of …
[HTML][HTML] The anionic chemistry of ynamides: A review
G Evano, B Michelet, C Zhang - Comptes Rendus Chimie, 2017 - Elsevier
Ynamides have recently evolved as remarkably reactive and versatile building blocks for
chemical synthesis. The development of efficient and robust methods for their preparation …
chemical synthesis. The development of efficient and robust methods for their preparation …
Photochemical Dual‐Catalytic Synthesis of Alkynyl Sulfides
J Santandrea, C Minozzi, C Cruché… - Angewandte Chemie …, 2017 - Wiley Online Library
A photochemical dual‐catalytic cross‐coupling to form alkynyl sulfides via C (sp)− S bond
formation is described. The cross‐coupling of thiols and bromoalkynes is promoted by a …
formation is described. The cross‐coupling of thiols and bromoalkynes is promoted by a …
Cross-dehydrogenative coupling reactions between C (sp)–H and X–H (X= N, P, S, Si, Sn) bonds: An environmentally benign access to heteroatom-substituted …
Form a green and sustainable chemistry point of view, cross-dehydrogenative coupling (or
oxidative cross-coupling) reactions have been recognized as environmentally sustainable …
oxidative cross-coupling) reactions have been recognized as environmentally sustainable …
Alkynyl triazenes as fluoroalkyne surrogates: regioselective access to 4-fluoro-2-pyridones by a Rh (III)-catalyzed C–H activation–Lossen rearrangement–Wallach …
Fluorinated pyridones are an important scaffold displaying relevant biological activities.
Efficient assembly strategies of pyridones are transition metal-catalyzed C–H annulations …
Efficient assembly strategies of pyridones are transition metal-catalyzed C–H annulations …
Palladium‐Catalyzed Silylcyanation of Ynamides: Regio‐and Stereoselective Access to Tetrasubstituted 3‐Silyl‐2‐Aminoacrylonitriles
P Hansjacob, FR Leroux, V Gandon… - Angewandte Chemie …, 2022 - Wiley Online Library
The palladium‐catalyzed silylcyanation of ynamides is described. This reaction is fully
regioselective, delivering tetrasubstituted 2‐aminoacrylonitriles derivatives exclusively …
regioselective, delivering tetrasubstituted 2‐aminoacrylonitriles derivatives exclusively …