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Selin Ezgi Donmez,
Onur Şahin and
Yunus Emre Türkmen

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NaI/PPh₃-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles

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Yue Zhao and
Frederic W. Patureau

Letter
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Beilstein J. Org. Chem. 2023, 19, 57–65, doi:10.3762/bjoc.19.5

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Modern flow chemistry – prospect and advantage

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Editorial
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Supporting Information File 1: Experimental procedures for the synthesis of new compounds and spectral data of new compounds including ¹H NMR, ¹³C NMR, and HMQC spectra.
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Redox active dendronized polystyrenes equipped with peripheral triarylamines

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Electrosynthesis

Latest Articles

1,4-Dithianes: attractive C2-building blocks for the synthesis of complex molecular architectures

Synthesis and characterisation of new antimalarial fluorinated triazolopyrazine compounds

Practical synthesis of isocoumarins via Rh(III)-catalyzed C–H activation/annulation cascade

Revisiting the bromination of 3β-hydroxycholest-5-ene with CBr₄/PPh₃ and the subsequent azidolysis of the resulting bromide, disparity in stereochemical behavior

Organophosphorus chemistry: from model to application

Preparation of β-cyclodextrin/polysaccharide foams using saponin

Catalytic aza-Nazarov cyclization reactions to access α-methylene-γ-lactam heterocycles

NaI/PPh₃-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles

Improving the accuracy of ³¹P NMR chemical shift calculations by use of scaling methods

Modern flow chemistry – prospect and advantage

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