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Bram Ryckaert,
Ellen Demeyere,
Frederick Degroote,
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Beilstein J. Org. Chem. 2023, 19, 115–132, doi:10.3762/bjoc.19.12

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Jonathan M. White,
Daniel J. G. Johnson,
Vicky M. Avery and
Rohan A. Davis

Full Research Paper
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Beilstein J. Org. Chem. 2023, 19, 107–114, doi:10.3762/bjoc.19.11

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

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Yi-Fei Li,
Jun Xuan and
Xiao-Qiang Hu

Letter
Published 30 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 100–106, doi:10.3762/bjoc.19.10

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

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Jas S. Ward,
Kari Rissanen,
Carsten Bolm and
Mohamed Ramadan El Sayed Aly

Full Research Paper
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Beilstein J. Org. Chem. 2023, 19, 91–99, doi:10.3762/bjoc.19.9

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Organophosphorus chemistry: from model to application

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Editorial
Published 25 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 89–90, doi:10.3762/bjoc.19.8

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Preparation of β-cyclodextrin/polysaccharide foams using saponin

Max Petitjean and
José Ramón Isasi

Full Research Paper
Published 24 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 78–88, doi:10.3762/bjoc.19.7

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

Bilge Banu Yagci,
Selin Ezgi Donmez,
Onur Şahin and
Yunus Emre Türkmen

Full Research Paper
Published 17 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 66–77, doi:10.3762/bjoc.19.6

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

Dan Liu,
Yue Zhao and
Frederic W. Patureau

Letter
Published 16 Jan 2023

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

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

William H. Hersh and
Tsz-Yeung Chan

Full Research Paper
Published 10 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 36–56, doi:10.3762/bjoc.19.4

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Modern flow chemistry – prospect and advantage

Philipp Heretsch

Editorial
Published 06 Jan 2023

Beilstein J. Org. Chem. 2023, 19, 33–35, doi:10.3762/bjoc.19.3

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Supporting Information File 1: Experimental procedures, spectroscopical data, X-ray analysis of 30, and NMR spectra plots.
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Synthesis of eunicellane-type bicycles embedding a 1,3-cyclohexadiene moiety

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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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