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Marek Kõllo,
Marje Kasari,
Villu Kasari,
Tõnis Pehk,
Ivar Järving,
Margus Lopp,
Arvi Jõers and
Tõnis Kanger

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Published 01 Mar 2021

Beilstein J. Org. Chem. 2021, 17, 581–588, doi:10.3762/bjoc.17.52

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Breakdown of 3-(allylsulfonio)propanoates in bacteria from the Roseobacter group yields garlic oil constituents

Anuj Kumar Chhalodia and
Jeroen S. Dickschat

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Beilstein J. Org. Chem. 2021, 17, 569–580, doi:10.3762/bjoc.17.51

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

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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

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Published 24 Feb 2021

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
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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

Lucía Rossi-Fernández,
Viviana Dorn and
Gabriel Radivoy

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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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Supporting Information File 1: Copies of NMR spectra for compounds 2, 3, 6, 7, 8, 10a and 10b and 11.
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Cited References
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Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon–carbon bond forming reactions

Supporting Information

References

Article is part of the issue

Superstructures with cyclodextrins: Chemistry and applications II

Latest Articles

Designed whole-cell-catalysis-assisted synthesis of 9,11-secosterols

Breakdown of 3-(allylsulfonio)propanoates in bacteria from the Roseobacter group yields garlic oil constituents

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

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