Cross-coupling of amides by N–C bond activation
G Meng, S Shi, M Szostak - Synlett, 2016 - thieme-connect.com
In recent years, significant conceptual advances have taken place in the field of amide bond
cross-coupling. Mild and selective functionalization of amides by transition-metal catalysis …
cross-coupling. Mild and selective functionalization of amides by transition-metal catalysis …
Development of novel methodology using diazo compounds and metal catalysts
S Harada - Chemical and Pharmaceutical Bulletin, 2021 - jstage.jst.go.jp
The ability to control the reactions of highly active chemical species to enable
straightforward synthesis of valuable compounds such as bioactive natural products and …
straightforward synthesis of valuable compounds such as bioactive natural products and …
Enantioselective construction of acyclic quaternary carbon stereocenters: palladium-catalyzed decarboxylative allylic alkylation of fully substituted amide enolates
P Starkov, JT Moore, DC Duquette… - Journal of the …, 2017 - ACS Publications
We report a divergent and modular protocol for the preparation of acyclic molecular
frameworks containing newly created quaternary carbon stereocenters. Central to this …
frameworks containing newly created quaternary carbon stereocenters. Central to this …
Decarbonylative methylation of aromatic esters by a nickel catalyst
T Okita, K Muto, J Yamaguchi - Organic letters, 2018 - ACS Publications
A Ni-catalyzed decarbonylative methylation of aromatic esters was achieved using
methylaluminums as methylating agents. Dimethylaluminum chlorides uniquely worked as …
methylaluminums as methylating agents. Dimethylaluminum chlorides uniquely worked as …
Protocol for Palladium/N-Heterocyclic Carbene-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides by N–C (O) Activation
Amides are among the most important and ubiquitous functional groups in organic chemistry
and process development. In this Practical Synthetic Procedure, a protocol for the Suzuki …
and process development. In this Practical Synthetic Procedure, a protocol for the Suzuki …
Urea Insertion Reaction of Rhodium-Carbenoid
Y Hashimoto, M Kono, S Harada… - Chemical and …, 2018 - jstage.jst.go.jp
We developed the first carbenoid insertion reaction into the urea C− N bond. The urea
insertion reaction proceeded smoothly using Rh 2 (NHPiv) 4, a rhodium catalyst previously …
insertion reaction proceeded smoothly using Rh 2 (NHPiv) 4, a rhodium catalyst previously …
Thieme Chemistry Journals Awardees–Where Are They Now? Bis (2-pyridyl) amides as Readily Cleavable Amides Under Catalytic, Neutral, and Room-Temperature …
S Adachi, N Kumagai, M Shibasaki - Synlett, 2018 - thieme-connect.com
Mild solvolytic cleavage of bis (2-pyridyl) amide under neutral and room-temperature
conditions is described. The inherently stable amide was readily activated by catalytic …
conditions is described. The inherently stable amide was readily activated by catalytic …