Results 191 to 200 of about 196,557 (349)
An iridium‐catalyzed linear‐selective sp3 C─H alkylation of N‐methylamides with alkenes is described. This method tolerates various N‐methylacetamide derivatives and has a broad alkene scope. Mechanistic studies were also conducted. Internal alkenes can also be used through in situ consecutive alkene isomerization.
Haluhi Takahashi, Takanori Shibata
wiley +1 more source
Frontiers in manganese catalysis: a sustainable platform for bond construction and heterocycle synthesis. [PDF]
Das AK +7 more
europepmc +1 more source
Selectivity in C-alkylation of dianions of protected 6-methyluridine [PDF]
Ngoc Hoa Nguyen +3 more
openalex +1 more source
Expedient Discovery of a Metallaphotoredox Cyanomethylation for Synthesizing α‐Aryl Nitriles
A metallaphotoredox cyanomethylation reaction has been developed for the synthesis of valuable α‐aryl nitrile intermediates. The methodology was successfully applied to diverse medicinally‐relevant substrates, providing an expedient route to anti‐cancer Senexin compounds, while also removing the need for toxic cyanide reagents. The mechanism was probed
Gemma C. Cook +6 more
wiley +1 more source
Routes to amino acid derivatives, rearrangements, condensations, and alkylations of schiff bases
Anne Wietze van der Werf
openalex +1 more source
Alkylation of N-Monosubstituted Diphenylphosphinamides
Yoshiko Kobayashi +2 more
openalex +2 more sources
Dearomative homocoupling of quinolines into 1,1',2,2',3,3',4,4'‐octahydro‐4,4'‐biquinoline (OHBQ) is reported. The photoexcited boron complex, in situ generated from quinoline, HB(pin), and KOtBu, enables the unprecedented homocoupling of tetrahydroquinolines that is challenging in the ground state, expanding the chemical diversity of OHBQ derivatives.
Mone Suzuki +2 more
wiley +1 more source
Site-specific ribozyme-mediated alkylation of DNA substrates. [PDF]
He Y +7 more
europepmc +1 more source
Potassium iodide catalysis in the alkylation of protected hydrazines; pp. 10–17
Anton Mastitski +3 more
openalex +1 more source
Monosubstituted N‐arylhydroxylamines represent a unique subclass of hydroxylamines that act as pivotal intermediates in redox transformations and as versatile platforms for further synthetic transformations. They serve as key building blocks in the synthesis of architecturally complex heterocycles and other valuable organic compounds.
Michael G. Kallitsakis +2 more
wiley +1 more source

