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Dileep Kumar Singh

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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

Dominic R. Willcox and
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Review
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Andreas Boelke and
Boris J. Nachtsheim

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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

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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
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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

Full Research Paper
Published 02 Mar 2023

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

Solomiia Borova and
Robert Luxenhofer

Full Research Paper
Published 28 Feb 2023

Beilstein J. Org. Chem. 2023, 19, 217–230, doi:10.3762/bjoc.19.21

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Friedel–Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs)

Swantje Lerch,
Stefan Fritsch and
Thomas Strassner

Full Research Paper
Published 23 Feb 2023

Beilstein J. Org. Chem. 2023, 19, 212–216, doi:10.3762/bjoc.19.20

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Supporting Information File 1: Experimental procedures and characterisation data of synthesised, previously unknown compounds.
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Regio- and stereoselective oxidation of unactivated C–H bonds with Rhodococcus rhodochrous

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Latest Articles

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

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

Friedel–Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs)

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