Ynamides: a modern functional group for the new millennium
Alkynes represent one of the most important and versatile building blocks in organic
synthesis. Heteroatom-substituted alkynes, which can be considered as subgroups of …
synthesis. Heteroatom-substituted alkynes, which can be considered as subgroups of …
Ynamides: versatile tools in organic synthesis
Ynamides display an exceptionally fine balance between stability and reactivity. They also
offer unique and multiple opportunities for the inclusion of nitrogen‐based functionalities into …
offer unique and multiple opportunities for the inclusion of nitrogen‐based functionalities into …
Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide
Dialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions
and have been applied in a range of contexts. This perspective attempts to aid the reader in …
and have been applied in a range of contexts. This perspective attempts to aid the reader in …
MOF catalysis in relation to their homogeneous counterparts and conventional solid catalysts
Metal–organic frameworks have recently attracted attention as heterogeneous catalysts due
to their high content of metal centres and large surface area and pore volume, along with …
to their high content of metal centres and large surface area and pore volume, along with …
Cu-catalyzed oxidative amidation of propiolic acids under air via decarboxylative coupling
W Jia, N Jiao - Organic Letters, 2010 - ACS Publications
Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling |
Organic Letters Recently Viewedclose modal ACS ACS Publications C&EN CAS Find my …
Organic Letters Recently Viewedclose modal ACS ACS Publications C&EN CAS Find my …
Gold-catalyzed synthesis of benzil derivatives and α-keto imides via oxidation of alkynes
CF Xu, M Xu, YX Jia, CY Li - Organic Letters, 2011 - ACS Publications
An efficient process based on the gold-catalyzed redox reaction has been developed to
oxidize 1, 2-diarylacetylene or ynamide to 1, 2-diaryldiketone or α-keto imide respectively …
oxidize 1, 2-diarylacetylene or ynamide to 1, 2-diaryldiketone or α-keto imide respectively …
General amination reactions for the synthesis of ynamides
The development of general syntheses of ynamides and related compounds based on
various amination strategies are described in this short review. Reactions are classified …
various amination strategies are described in this short review. Reactions are classified …
Highly regioselective Au (I)-catalyzed hydroamination of ynamides and propiolic acid derivatives with anilines
S Kramer, K Dooleweerdt, AT Lindhardt… - Organic …, 2009 - ACS Publications
A highly regioselective hydroamination of unsymmetrical electron-poor and electron-rich
alkynes with anilines catalyzed by Au (I) under mild conditions is reported. In addition …
alkynes with anilines catalyzed by Au (I) under mild conditions is reported. In addition …
A robust and modular synthesis of ynamides
A flexible, modular ynamide synthesis is reported that uses trichloroethene as an
inexpensive two carbon synthon. A wide range of amides and electrophiles can be …
inexpensive two carbon synthon. A wide range of amides and electrophiles can be …
Sequential and One-Pot Reactions of Phenols with Bromoalkynes for the Synthesis of (Z)-2-Bromovinyl Phenyl Ethers and Benzo[b]furans
S Wang, P Li, L Yu, L Wang - Organic Letters, 2011 - ACS Publications
Benzo [b] furans were prepared in one pot based on the addition/palladium-catalyzed C–H
bond functionalization of phenols with bromoalkynes. The addition reactions of phenols to …
bond functionalization of phenols with bromoalkynes. The addition reactions of phenols to …