Triplet Energy Transfer-Driven Intermolecular [2+2] Photocycloaddition of Acyclic Imines and Indoles: Facile Access to Azetidine-Fused Indolines. [PDF]
Yang G, Han Z, Zhang H, Cui X.
europepmc +1 more source
A metal‐ and oxidant‐free electrochemical multicomponent di‐functionalization strategy that rapidly converts 1,1‐disubstituted alkenes into α‐tertiary primary amines with simultaneous installation of bio‐relevant sulfur or selenium motifs was devised for late‐stage functionalization. ABSTRACT Quaternary carbon centers, especially those bearing nitrogen,
Adrija Ghosh +4 more
wiley +1 more source
The Staudinger reaction: a versatile synthetic tool for the construction of β-lactams, heterocycles, and functional organic molecules. [PDF]
Mughal EU +8 more
europepmc +1 more source
Nitrogen Radical Photocatalysed Reduction of Nitrous Oxide
This work offers the first example of reduction of the potent greenhouse gas N2O to the benign products N2 and O(Bpin)2 using a nitrogen‐based catalyst. The active catalyst is shown to be a nitrogen‐based radical which operates under photocatalytic conditions.
Reece Lister‐Roberts +2 more
wiley +1 more source
High-entropy photocatalyst enabling collaborative cascade C-N coupling for converting benzyl alcohol to imine. [PDF]
Yang N +6 more
europepmc +1 more source
The first nitrile reductive couplings beyond stoichiometric metals or metalloids are described. Using a ruthenium catalyst derived from RuHCl(CO)(PPh3)3 and Cy‐BIPHEP, 2‐propanol‐mediated reductive coupling of phenyl acrylate with aromatic or aliphatic nitriles delivers α,β‐unsaturated β‐amino esters.
Sebastian Höthker +3 more
wiley +1 more source
Cobalt-catalyzed asymmetric three-component reductive addition of alkynes with alkyl halides and imines. [PDF]
Hou L, Wu W, Wang Z, Wu X, Qu J, Chen Y.
europepmc +1 more source
Oxidative Coupling of Alcohols and Amines Using Functionalized Cu(II) 2‑Quinoxolinol Salen Catalysts. [PDF]
Huo X +5 more
europepmc +1 more source
Unified Synthesis of Unconventional α‐Polyhalogenated Amines Through Hydroaminoalkylation
A unified, redox‐neutral method that transforms alkenes and alkynes into α‐polyhalomethyl amines using stable hemiaminal reagents is reported. This approach enables access to CF3, CF2H, CF2Cl, and CFClH motifs, expanding halogenated amine space with broad substrate scope, functional group tolerance, and applicability to late‐stage modification of drug ...
Angela K. Hofmeister +9 more
wiley +1 more source
Design, Synthesis, and Biological Evaluation of Trifluoromethylated 1,2,4-Triazin-6-ones with Selective Antimycotic Activity and Hormesis Effects. [PDF]
Kowalczyk A +6 more
europepmc +1 more source

