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Cristina L. Mitroi,
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Review
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Beilstein J. Org. Chem. 2023, 19, 349–379, doi:10.3762/bjoc.19.29

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Beilstein J. Org. Chem. 2023, 19, 317–324, doi:10.3762/bjoc.19.27

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Recommendations for performing measurements of apparent equilibrium constants of enzyme-catalyzed reactions and for reporting the results of these measurements

Robert N. Goldberg,
Robert T. Giessmann,
Peter J. Halling,
Carsten Kettner and
Hans V. Westerhoff

Perspective
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Beilstein J. Org. Chem. 2023, 19, 303–316, doi:10.3762/bjoc.19.26

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Continuous flow synthesis of 6-monoamino-6-monodeoxy-β-cyclodextrin

János Máté Orosz,
Dóra Ujj,
Petr Kasal,
Gábor Benkovics and
Erika Bálint

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Juraj Kóňa,
Maroš Bella and
Monika Poláková

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Beilstein J. Org. Chem. 2023, 19, 282–293, doi:10.3762/bjoc.19.24

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Charlène Gadais,
Laurent Legentil and
François-Hugues Porée

Review
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Vaishali,
Rahul Jamra,
Naveen Banyal,
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Beilstein J. Org. Chem. 2023, 19, 231–244, doi:10.3762/bjoc.19.22

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Investigation of cationic ring-opening polymerization of 2-oxazolines in the “green” solvent dihydrolevoglucosenone

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Latest Articles

Combretastatins D series and analogues: from isolation, synthetic challenges and biological activities

Discrimination of β-cyclodextrin/hazelnut (Corylus avellana L.) oil/flavonoid glycoside and flavonolignan ternary complexes by Fourier-transform infrared spectroscopy coupled with principal component analysis

CuAAC-inspired synthesis of 1,2,3-triazole-bridged porphyrin conjugates: an overview

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Recommendations for performing measurements of apparent equilibrium constants of enzyme-catalyzed reactions and for reporting the results of these measurements

Continuous flow synthesis of 6-monoamino-6-monodeoxy-β-cyclodextrin

Synthesis, α-mannosidase inhibition studies and molecular modeling of 1,4-imino-ᴅ-lyxitols and their C-5-altered N-arylalkyl derivatives

Strategies to access the [5-8] bicyclic core encountered in the sesquiterpene, diterpene and sesterterpene series

An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides

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