Synthesis, structural characterization, and optical properties of benzo[f]naphtho[2,3-b]phosphoindoles

Mio Matsumura,
Takahiro Teramoto,
Masato Kawakubo,
Masatoshi Kawahata,
Yuki Murata,
Kentaro Yamaguchi,
Masanobu Uchiyama and
Shuji Yasuike

Letter
Published 05 Mar 2021

Beilstein J. Org. Chem. 2021, 17, 671–677, doi:10.3762/bjoc.17.56

Full Text

[2 + 1] Cycloaddition reactions of fullerene C₆₀ based on diazo compounds

Yuliya N. Biglova

Review
Published 05 Mar 2021

Beilstein J. Org. Chem. 2021, 17, 630–670, doi:10.3762/bjoc.17.55

Full Text

Synthesis and properties of oligonucleotides modified with an N-methylguanidine-bridged nucleic acid (GuNA[Me]) bearing adenine, guanine, or 5-methylcytosine nucleobases

Naohiro Horie,
Takao Yamaguchi,
Shinji Kumagai and
Satoshi Obika

Full Research Paper
Published 04 Mar 2021

Beilstein J. Org. Chem. 2021, 17, 622–629, doi:10.3762/bjoc.17.54

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Valorisation of plastic waste via metal-catalysed depolymerisation

Francesca Liguori,
Carmen Moreno-Marrodán and
Pierluigi Barbaro

Review
Published 02 Mar 2021

Beilstein J. Org. Chem. 2021, 17, 589–621, doi:10.3762/bjoc.17.53

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

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

Full Research Paper
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

Full Research Paper
Published 26 Feb 2021

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

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

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
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
Published 23 Feb 2021

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

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Supporting Information File 1: DMSP demethylation pathway in Celeribacter spp. and copies of spectra.
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Identification of volatiles from six marine Celeribacter strains

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Chemical ecology

Latest Articles

Synthesis, structural characterization, and optical properties of benzo[f]naphtho[2,3-b]phosphoindoles

[2 + 1] Cycloaddition reactions of fullerene C₆₀ based on diazo compounds

Synthesis and properties of oligonucleotides modified with an N-methylguanidine-bridged nucleic acid (GuNA[Me]) bearing adenine, guanine, or 5-methylcytosine nucleobases

Valorisation of plastic waste via metal-catalysed depolymerisation

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

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