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

Jorge de Lima Neto and
Paulo Henrique Menezes

Review
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Beilstein J. Org. Chem. 2023, 19, 399–427, doi:10.3762/bjoc.19.31

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Gabriela Popescu,
Dina Gligor (Pane),
Cristina L. Mitroi,
Sorin M. Stanciu and
Daniel Ioan Hădărugă

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Beilstein J. Org. Chem. 2023, 19, 380–398, doi:10.3762/bjoc.19.30

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Dileep Kumar Singh

Review
Published 22 Mar 2023

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

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Group 13 exchange and transborylation in catalysis

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Review
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Beilstein J. Org. Chem. 2023, 19, 325–348, doi:10.3762/bjoc.19.28

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Annalena Dietz,
Andreas Boelke and
Boris J. Nachtsheim

Full Research Paper
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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
Published 15 Mar 2023

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

Full Research Paper
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Beilstein J. Org. Chem. 2023, 19, 294–302, doi:10.3762/bjoc.19.25

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

Martin Kalník,
Sergej Šesták,
Juraj Kóňa,
Maroš Bella and
Monika Poláková

Full Research Paper
Published 06 Mar 2023

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

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

Cécile Alleman,
Charlène Gadais,
Laurent Legentil and
François-Hugues Porée

Review
Published 03 Mar 2023

Beilstein J. Org. Chem. 2023, 19, 245–281, doi:10.3762/bjoc.19.23

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

Shubham Sharma,
Dharmender Singh,
Sunit Kumar,
Vaishali,
Rahul Jamra,
Naveen Banyal,
Deepika,
Chandi C. Malakar and
Virender Singh

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Beilstein J. Org. Chem. 2023, 19, 231–244, doi:10.3762/bjoc.19.22

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Supporting Information File 1: Analytic data and copies of ¹H, ¹³C, and ³¹P NMR spectra of compounds 3.
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Efficient synthesis of ethyl 2-(oxazolin-2-yl)alkanoates via ethoxycarbonylketene-induced electrophilic ring expansion of aziridines

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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

Group 13 exchange and transborylation in catalysis

Synthesis and reactivity of azole-based iodazinium salts

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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