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Beilstein J. Org. Chem. 2019, 15, 1321–1330, doi:10.3762/bjoc.15.131

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Iva Jušinski,
Davor Gracin and
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Anastasiya E. Sibiryakova,
Marat R. Baimuratov,
Eugene V. Golovin,
Victor B. Rybakov and
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Beilstein J. Org. Chem. 2019, 15, 1289–1297, doi:10.3762/bjoc.15.127

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Doebner-type pyrazolopyridine carboxylic acids in an Ugi four-component reaction

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Oleksandr V. Kolomiets,
Maryna M. Kornet,
Yana I. Sakhno,
Sergey M. Desenko,
Victoriya V. Dyakonenko,
Svetlana V. Shishkina,
Oleksandr A. Brazhko,
Vladimir I. Musatov,
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Supporting Information File 1: NMR spectra of azobenzene 5, UV–vis data and detailed procedures, details for conformational analysis and DFT computations.
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London dispersion as important factor for the stabilization of (Z)-azobenzenes in the presence of hydrogen bonding

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Dispersion interactions

Latest Articles

Anomeric sugar boronic acid analogues as potential agents for boron neutron capture therapy

Formation of an unexpected 3,3-diphenyl-3H-indazole through a facile intramolecular [2 + 3] cycloaddition of the diazo intermediate

Efficient resolution of racemic crown-shaped cyclotriveratrylene derivatives and isolation and characterization of the intermediate saddle isomer

Synthesis of dipolar molecular rotors as linkers for metal-organic frameworks

Host–guest interactions between p-sulfonatocalix[4]arene and p-sulfonatothiacalix[4]arene and group IA, IIA and f-block metal cations: a DFT/SMD study

Mechanochemical Friedel–Crafts acylations

Enantioselective Diels–Alder reaction of anthracene by chiral tritylium catalysis

Genomics-inspired discovery of massiliachelin, an agrochelin epimer from Massilia sp. NR 4-1

Synthesis of non-racemic 4-nitro-2-sulfonylbutan-1-ones via Ni(II)-catalyzed asymmetric Michael reaction of β-ketosulfones

Doebner-type pyrazolopyridine carboxylic acids in an Ugi four-component reaction

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