Results 171 to 180 of about 29,422 (294)

Activation of Aryl Halides by Triplet–Triplet Annihilation Upconversion Enabling Coupling Processes Under an Open‐to‐Air Environment

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Triplet–triplet annihilation upconversion (TTA‐UC) performed inside supramolecular viscoelastic gels enables efficient CC and C–heteroatom coupling reactions under green LED irradiation in open‐air conditions. The gel network restricts oxygen diffusion, preserves triplet states, and allows aryl halide activation through upconverted excited states ...
Daniel Álvarez‐Gutiérrez   +4 more
wiley   +1 more source

Photochemical C4-Selective C-H Amination of Quinolines via <i>N</i>-Shift of Heteroaryl Azides. [PDF]

open access: yesOrg Lett
Dimasi A   +5 more
europepmc   +1 more source

A Short Total Synthesis of the Daucane Sesquiterpenoid Ferutinin

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Only nine steps were required to access the bioactive daucane sesquiterpene ester ferutinin (1) from 3‐methyl‐2‐cyclopentenone (3) and allyl p‐tolyl sulfoxide. A one‐pot 1,4‐addition/aldol sequence was used to rapidly provide diene 2 (TBS = tert‐butyldimethylsilyl), ring‐closing metathesis of which followed by alkylation and acylation gave rise to the ...
Christiane Osthaar   +3 more
wiley   +1 more source

Electrochemical Three‐Component Synthesis of Heteroaryl Sulfonates

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
An electrochemical, metal‐free three‐component strategy for direct C(sp2)─H sulfonation of electron‐rich heteroarenes using SO2 and alcohols is described. Utilizing inexpensive graphite electrodes and practical SO2 stock solutions under mild conditions, this method provides straightforward access to heteroaryl sulfonates from simple building blocks ...
Po‐Chung Chien   +2 more
wiley   +1 more source

One‐Pot Gold(I)‐Catalyzed Rautenstrauch Rearrangement/Nitrosocarbonyl Hetero‐Diels–Alder Reaction Sequence for the Synthesis of α‐Hydroxylated Cyclopentenones

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
The regio‐ and stereoselective synthesis of ring‐fused α‐hydroxy‐2‐cyclopentenones is achieved by a one‐pot gold(I)‐catalyzed Rautenstrauch rearrangement/nitrosocarbonyl hetero‐Diels–Alder reaction/ring opening sequence carried out on suitable propargyl esters followed by selective NO bond cleavage.
Dina Scarpi   +3 more
wiley   +1 more source

Total Synthesis of Sacrolide A and Cytotoxic Evaluation

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Isolated from the edible cyanobacterium Aphanothece sacrum, sacrolide A is a highly potent antimicrobial and cytotoxic metabolite. Its total synthesis via a convergent strategy enabled accurate assessment of its effects on liver and colon cells, offering new insights into its bioactivity and potential health risks.
Priyanka Kataria   +7 more
wiley   +1 more source

Narrowband Macrocycles: A New Paradigm for High‐Color‐Purity Organic Light‐Emitting Diodes

open access: yesFlexTech, EarlyView.
This graphical abstract illustrates two key strategies for constructing macrocyclic multi‐resonance (MR) emitters for high‐performance OLEDs: (1) the covalent assembly of MR moieties onto macrocyclic scaffolds, and (2) the local multi‐resonance strategy within the macrocyclic backbone.
Zhongbo Xiang   +3 more
wiley   +1 more source

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