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Bram Ryckaert,
Ellen Demeyere,
Frederick Degroote,
Hilde Janssens and
Johan M. Winne

Review
Published 02 Feb 2023

Beilstein J. Org. Chem. 2023, 19, 115–132, doi:10.3762/bjoc.19.12

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Synthesis and characterisation of new antimalarial fluorinated triazolopyrazine compounds

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

Full Research Paper
Published 31 Jan 2023

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

Qian-Ci Gao,
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

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

Full Research Paper
Published 27 Jan 2023

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

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Organophosphorus chemistry: from model to application

György Keglevich

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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Cited References
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EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters

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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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