Results 91 to 100 of about 6,583 (223)
Clean and fast cross-coupling of aryl halides in one-pot
Unsymmetrically coupled biaryls are synthesized in high yield starting from different aryl bromides and bis(pinacolato)diboron by carrying out the Miyaura borylation reaction followed by the Suzuki–Miyaura reaction in the same reaction pot over 1–2 mol %
Valerica Pandarus +4 more
doaj +1 more source
Late-stage functionalization of natural products and pharmaceuticals use CH functionalization to diversify the complex motif late in the synthesis accessing a large number of complex derivatives in a single step.
Bray, Jean +3 more
core
Donor–acceptor and donor–donor systems incorporating an indeno[1,2‐b]fluorene‐extended tetrathiafulvalene (IF‐TTF) donor motif were prepared by Suzuki coupling reactions. The compounds were studied for their optical and redox properties. The compounds showed multiredox behavior with several accessible redox states. A series of π‐extended donor–acceptor
Cecilie Rindom +1 more
wiley +1 more source
A data‐driven discovery engine—exhaustive enumeration of carbazole‐containing polycyclic aromatic hydrocarbons (Cz‐PAHs) followed by machine learning—identifies boron‐free, narrowband blue thermally activated delayed fluorescence emitters for organic light‐emitting diodes (OLEDs).
Masaya Hagai +6 more
wiley +2 more sources
A methodology for the solid-phase synthesis of biaryl bicyclic peptides containing a Phe-Phe, a Phe-Tyr or a Tyr-Tyr motif has been devised. This approach comprises two key steps.
Iteng Ng-Choi +3 more
doaj +1 more source
Combining the Heck reaction with other transformations provides a powerful strategy to access diverse, complex compounds. Here, the authors report a weak coordination dominated Pd(0)-catalyzed quadruple C-H activation followed by hydro-functionalization,
Bo-Cheng Tang +7 more
doaj +1 more source
Nucleophilic Reactions of Cyclobutenones and the Related 4,4‐Dichlorocyclobutenone Derivatives
Cyclobutenone derivates and their 4,4‐dichloro counterparts have an uninterrupted attention as useful synthons in the synthesis of complex organic molecules. Their nucleophilic reactions remain underexplored. This review brings attention to these reactions, whose outcome is not straightforward.
Sarah J. Wright +2 more
wiley +1 more source
An orthogonal spirobifluorene‐fusion strategy is introduced for B/N/O‐alternated MR frameworks, enabling improved kRISC (5.46 × 103 s−1), high ΦPL (97%), and narrow‐band pure‐red emission. Vacuum‐evaporated OLEDs incorporating this emitter achieve an EQEmax >40% (FWHM = 36 nm) and exhibit exceptionally low efficiency roll‐off at high luminance ...
Yan‐Yun Jing +7 more
wiley +1 more source
Mechanochemical borylation of aryldiazonium salts; merging light and ball milling
Merging of photo- and mechanochemical activation permitted studying the role of eosin Y in the borylation of aryldiazonium salts in a ball mill. Simultaneous neat grinding/irradiation of the reactants and the photocatalyst led to the formation of ...
José G. Hernández
doaj +1 more source
Integrating carbonyl lock onto multi‐resonant organoboron emitters is found to go beyond conventional bridge unit. It can not only suppress the molecular relaxation as conventional bridge, but also substantially affect electronic engineering via carbonyl integration, activating multiple up‐conversion channels, thus leading to an accelerated spin‐flip ...
Tingfeng Chen +7 more
wiley +1 more source

