Results 181 to 190 of about 607,889 (218)
Chalcogen‐based compounds are explored as versatile tools to enhance the stability and performance of halide perovskites. Their roles in defect passivation, ion migration suppression, and interface engineering are analyzed, along with impacts on device efficiency.
Atanu Jana +4 more
wiley +1 more source
Surface‐localized Ag domains on PdCu nanowires enhance *OH adsorption while preserving contiguous PdCu ensembles, enabling rapid removal of poisoning intermediates and facilitating C–C bond cleavage during alkaline ethanol oxidation. The optimized Pd1Cu1@Ag0.25 catalyst combines high mass activity with enhanced C1 selectivity, highlighting spatially ...
Mengting Chen +10 more
wiley +1 more source
Oxidative Generation and Reactivity of the Cyclopropyl Radical From a Martin Silicate
A photoredox strategy employing Martin silicates enables the oxidative generation and controlled capture of cyclopropyl radicals, including the naked one, long considered challenging intermediates. The method affords functionalized cyclopropanes through both Giese‐type additions and dual nickel/photoredox C(sp3)−C(sp2) cross‐couplings.
Amal Lakhal +3 more
wiley +1 more source
ATRP depolymerization of lignin-derived polymethacrylates.
Mountaki SA +4 more
europepmc +1 more source
Alcohol/Water-Relay Sulfurative Oxygenation of Vinyl Bromides Enabled by Photoinduced EDA Complexes. [PDF]
Karmakar I +4 more
europepmc +1 more source
Synthesis of Oligonucleotide Conjugates Employing a Diselenide Linker
ABSTRACT In this study, we report the synthesis of an alkylene linker containing a terminal 2‐cyanoethyl protected selenium functionality for coupling at the 5'‐end of an oligonucleotide by solid phase synthesis for the preparation of oligonucleotide conjugates.
Shivam Tikoo +2 more
wiley +1 more source
Stereochemical Control in the Matteson Reaction
The Matteson homologation is a highly versatile method for the stereoselective insertion of carbenoids into boronic esters. Through iterative application of the process, complex chiral molecules can be synthesized. The stereoselectivity of the reaction is determined by a chiral diol incorporated in the boronic ester.
Hae Mo Lee, Christoph Hirschhäuser
wiley +1 more source
Vicinal disubstitution of alkyl C-X synthons via alkene radical cation generation. [PDF]
Zhang Y +11 more
europepmc +1 more source
A library of 21 tetrakis(phenothiazinyl)‐substituted silanes with broadly variable substituent decoration, which are fully reversible multistage redox systems with intense tunable emission from deep blue to yellow–green (441–533 nm), was rapidly synthesized by bromine–lithium exchange/borylation–Suzuki coupling of tetrakis(4‐bromophenyl)silane or by ...
Thomas P. M. Merke +4 more
wiley +1 more source
Decarbonylation Enables Chemodivergent Access to Guaiazulene-3-Oxalic and -Carboxylic Acid Derivatives. [PDF]
Audi E +8 more
europepmc +1 more source

