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

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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

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Lukáš Kolman,
Jiří Váňa,
Jan Svoboda and
Jiří Hanusek

Full Research Paper
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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

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Viviana Dorn and
Gabriel Radivoy

Full Research Paper
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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
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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

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Published 16 Feb 2021

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

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Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement

Vladimir Kubyshkin,
Rebecca Davis and
Nediljko Budisa

Review
Published 15 Feb 2021

Beilstein J. Org. Chem. 2021, 17, 439–460, doi:10.3762/bjoc.17.40

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Supporting Information File 1: Additional experimental and analytical data.
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Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate

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Organo-fluorine chemistry V

Latest Articles

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

Synthetic strategies of phosphonodepsipeptides

Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement

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