Group 13 exchange and transborylation in catalysis

Dominic R. Willcox and
Stephen P. Thomas

Review
Published 21 Mar 2023

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

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Synthesis and reactivity of azole-based iodazinium salts

Thomas J. Kuczmera,
Annalena Dietz,
Andreas Boelke and
Boris J. Nachtsheim

Full Research Paper
Published 16 Mar 2023

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

Full Text

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
Published 09 Mar 2023

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

Full Text

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

Full Text

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

Full Text

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

Full Text

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

Full Text

An accelerated Rauhut–Currier dimerization enabled the synthesis of (±)-incarvilleatone and anticancer studies

Tharun K. Kotammagari,
Sweta Misra,
Sayantan Paul,
Sunita Kunte,
Rajesh G. Gonnade,
Manas K. Santra and
Asish K. Bhattacharya

Full Research Paper
Published 21 Feb 2023

Beilstein J. Org. Chem. 2023, 19, 204–211, doi:10.3762/bjoc.19.19

Full Text

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Polymer and small molecule mechanochemistry: closer than ever

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Mechanochemistry III

Latest Articles

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)

An accelerated Rauhut–Currier dimerization enabled the synthesis of (±)-incarvilleatone and anticancer studies

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