Results 91 to 100 of about 6,583 (223)

Clean and fast cross-coupling of aryl halides in one-pot

open access: yesBeilstein Journal of Organic Chemistry, 2014
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

Borylation of Thioethers

open access: yes, 2023
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  

Modular π‐Extended IF‐TTF Systems: Tuning Redox and Optical Properties in Donor–Acceptor and Donor–Donor Frameworks

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
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

Machine‐Learning‐Guided Discovery of Boron‐Free Narrowband Blue Thermally Activated Delayed Fluorescence Emitters

open access: yesAngewandte Chemie, Volume 138, Issue 39, 21 September 2026.
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

Solid-phase synthesis of biaryl bicyclic peptides containing a 3-aryltyrosine or a 4-arylphenylalanine moiety

open access: yesBeilstein Journal of Organic Chemistry, 2019
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

Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst

open access: yesNature Communications, 2020
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

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
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

Spirobifluorene fusion in multiple resonance frameworks enables efficient pure‐red OLEDs with narrowband emission and suppressed efficiency roll‐off

open access: yesFlexMat, EarlyView.
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

open access: yesBeilstein Journal of Organic Chemistry, 2017
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

Carbonyl lock enables multi‐resonant organoboron framework with substantially enhanced spin‐flip and reduced emission bandwidth

open access: yesFlexMat, EarlyView.
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

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