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Zbigniew Malinowski,
Emilia Fornal,
Agata Sumara,
Renata Kontek,
Karol Bukowski,
Beata Pasternak,
Dariusz Sroczyński,
Joachim Kusz,
Magdalena Małecka and
Monika Nowak

Full Research Paper
Published 25 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 558–568, doi:10.3762/bjoc.17.50

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Metal-free visible-light-enabled vicinal trifluoromethyl dithiolation of unactivated alkenes

Xiaojuan Li,
Qiang Zhang,
Weigang Zhang,
Jinzhu Ma,
Yi Wang and
Yi Pan

Full Research Paper
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Beilstein J. Org. Chem. 2021, 17, 551–557, doi:10.3762/bjoc.17.49

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Menthyl esterification allows chiral resolution for the synthesis of artificial glutamate analogs

Kenji Morokuma,
Shuntaro Tsukamoto,
Kyosuke Mori,
Kei Miyako,
Ryuichi Sakai,
Raku Irie and
Masato Oikawa

Full Research Paper
Published 24 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 540–550, doi:10.3762/bjoc.17.48

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Synthesis of (Z)-3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones using an Eschenmoser coupling reaction

Lukáš Marek,
Lukáš Kolman,
Jiří Váňa,
Jan Svoboda and
Jiří Hanusek

Full Research Paper
Published 23 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 527–539, doi:10.3762/bjoc.17.47

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A new and efficient methodology for olefin epoxidation catalyzed by supported cobalt nanoparticles

Lucía Rossi-Fernández,
Viviana Dorn and
Gabriel Radivoy

Full Research Paper
Published 22 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 519–526, doi:10.3762/bjoc.17.46

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Synthesis and physicochemical evaluation of fluorinated lipopeptide precursors of ligands for microbubble targeting

Masayori Hagimori,
Estefanía E. Mendoza-Ortega and
Marie Pierre Krafft

Full Research Paper
Published 19 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 511–518, doi:10.3762/bjoc.17.45

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Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes

Olga Bakhanovich,
Viktor Khutorianskyi,
Vladimir Motornov and
Petr Beier

Full Research Paper
Published 18 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 504–510, doi:10.3762/bjoc.17.44

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The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst

Deniz Tözendemir and
Cihangir Tanyeli

Full Research Paper
Published 18 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 494–503, doi:10.3762/bjoc.17.43

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Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines

Geetanjali S. Sontakke,
Rahul K. Shukla and
Chandra M. R. Volla

Letter
Published 17 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 485–493, doi:10.3762/bjoc.17.42

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Synthetic strategies of phosphonodepsipeptides

Jiaxi Xu

Review
Published 16 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 461–484, doi:10.3762/bjoc.17.41

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Supporting Information File 1: 1D and 2D NMR spectra of all new compounds. Table of bond lengths for VHF 2 (X-ray crystallographic data). Exponential fit of the decay over time of the VHF 7 absorbance at the longest-wavelength absorption maximum.
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On the bromination of the dihydroazulene/vinylheptafulvene photo-/thermoswitch

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Molecular switches and cages

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Amino- and polyaminophthalazin-1(2H)-ones: synthesis, coordination properties, and biological activity

Metal-free visible-light-enabled vicinal trifluoromethyl dithiolation of unactivated alkenes

Menthyl esterification allows chiral resolution for the synthesis of artificial glutamate analogs

Synthesis of (Z)-3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones using an Eschenmoser coupling reaction

A new and efficient methodology for olefin epoxidation catalyzed by supported cobalt nanoparticles

Synthesis and physicochemical evaluation of fluorinated lipopeptide precursors of ligands for microbubble targeting

Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes

The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst

Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines

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