Synthesis and characterization of S,N-heterotetracenes

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Florian Henne,
Christoph Wetzel,
Elena Mena-Osteritz and
Peter Bäuerle

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Beilstein J. Org. Chem. 2020, 16, 2636–2644, doi:10.3762/bjoc.16.214

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Activation of pentafluoropropane isomers at a nanoscopic aluminum chlorofluoride: hydrodefluorination versus dehydrofluorination

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Thomas Braun,
Mike Ahrens and
Erhard Kemnitz

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Beilstein J. Org. Chem. 2020, 16, 2623–2635, doi:10.3762/bjoc.16.213

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Anion exchange resins in phosphate form as versatile carriers for the reactions catalyzed by nucleoside phosphorylases

Julia N. Artsemyeva,
Ekaterina A. Remeeva,
Tatiana N. Buravskaya,
Irina D. Konstantinova,
Roman S. Esipov,
Anatoly I. Miroshnikov,
Natalia M. Litvinko and
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Beilstein J. Org. Chem. 2020, 16, 2607–2622, doi:10.3762/bjoc.16.212

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Sébastien Saitzek,
Eric Monflier and
Frédéric Hapiot

Full Research Paper
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Beilstein J. Org. Chem. 2020, 16, 2598–2606, doi:10.3762/bjoc.16.211

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Synthesis of 4-substituted azopyridine-functionalized Ni(II)-porphyrins as molecular spin switches

Jannis Ludwig,
Tobias Moje,
Fynn Röhricht and
Rainer Herges

Full Research Paper
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Beilstein J. Org. Chem. 2020, 16, 2589–2597, doi:10.3762/bjoc.16.210

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Thermodynamic and electrochemical study of tailor-made crown ethers for redox-switchable (pseudo)rotaxanes

Henrik Hupatz,
Marius Gaedke,
Hendrik V. Schröder,
Julia Beerhues,
Arto Valkonen,
Fabian Klautzsch,
Sebastian Müller,
Felix Witte,
Kari Rissanen,
Biprajit Sarkar and
Christoph A. Schalley

Full Research Paper
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Beilstein J. Org. Chem. 2020, 16, 2576–2588, doi:10.3762/bjoc.16.209

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Synthesis of novel fluorinated building blocks via halofluorination and related reactions

Attila Márió Remete,
Tamás T. Novák,
Melinda Nonn,
Matti Haukka,
Ferenc Fülöp and
Loránd Kiss

Full Research Paper
Published 16 Oct 2020

Beilstein J. Org. Chem. 2020, 16, 2562–2575, doi:10.3762/bjoc.16.208

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Water-soluble host–guest complexes between fullerenes and a sugar-functionalized tribenzotriquinacene assembling to microspheres

Si-Yuan Liu,
Xin-Rui Wang,
Man-Ping Li,
Wen-Rong Xu and
Dietmar Kuck

Full Research Paper
Published 14 Oct 2020

Beilstein J. Org. Chem. 2020, 16, 2551–2561, doi:10.3762/bjoc.16.207

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Comparative ligand structural analytics illustrated on variably glycosylated MUC1 antigen–antibody binding

Christopher B. Barnett,
Tharindu Senapathi and
Kevin J. Naidoo

Full Research Paper
Published 13 Oct 2020

Beilstein J. Org. Chem. 2020, 16, 2540–2550, doi:10.3762/bjoc.16.206

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A new method for the synthesis of diamantane by hydroisomerization of binor-S on treatment with sulfuric acid

Rishat I. Aminov and
Ravil I. Khusnutdinov

Full Research Paper
Published 12 Oct 2020

Beilstein J. Org. Chem. 2020, 16, 2534–2539, doi:10.3762/bjoc.16.205

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Supporting Information File 1: Synthetic procedures, characterization data, SFC and HPLC conditions and copies of ¹H and ¹³C NMR spectra of new compounds.
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Hierarchically assembled helicates as reaction platform – from stoichiometric Diels–Alder reactions to enamine catalysis

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Molecular recognition

Latest Articles

Synthesis and characterization of S,N-heterotetracenes

Activation of pentafluoropropane isomers at a nanoscopic aluminum chlorofluoride: hydrodefluorination versus dehydrofluorination

Anion exchange resins in phosphate form as versatile carriers for the reactions catalyzed by nucleoside phosphorylases

Particle size effect in the mechanically assisted synthesis of β-cyclodextrin mesitylene sulfonate

Synthesis of 4-substituted azopyridine-functionalized Ni(II)-porphyrins as molecular spin switches

Thermodynamic and electrochemical study of tailor-made crown ethers for redox-switchable (pseudo)rotaxanes

Synthesis of novel fluorinated building blocks via halofluorination and related reactions

Water-soluble host–guest complexes between fullerenes and a sugar-functionalized tribenzotriquinacene assembling to microspheres

Comparative ligand structural analytics illustrated on variably glycosylated MUC1 antigen–antibody binding

A new method for the synthesis of diamantane by hydroisomerization of binor-S on treatment with sulfuric acid

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