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Yin Chen,
Jinqiu Ren,
Ruimin Yang,
Jie Li,
Sheng-Xiong Huang and
Yijun Yan

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Beilstein J. Org. Chem. 2022, 18, 1009–1016, doi:10.3762/bjoc.18.101

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Automated grindstone chemistry: a simple and facile way for PEG-assisted stoichiometry-controlled halogenation of phenols and anilines using N-halosuccinimides

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Jing Sun and
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Beilstein J. Org. Chem. 2022, 18, 991–998, doi:10.3762/bjoc.18.99

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First example of organocatalysis by cathodic N-heterocyclic carbene generation and accumulation using a divided electrochemical flow cell

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Richard C. D. Brown and
Marta Feroci

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Beilstein J. Org. Chem. 2022, 18, 979–990, doi:10.3762/bjoc.18.98

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Understanding the competing pathways leading to hydropyrene and isoelisabethatriene

Shani Zev,
Marion Ringel,
Ronja Driller,
Bernhard Loll,
Thomas Brück and
Dan T. Major

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Beilstein J. Org. Chem. 2022, 18, 972–978, doi:10.3762/bjoc.18.97

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Electrochemical and spectroscopic properties of twisted dibenzo[g,p]chrysene derivatives

Tomoya Imai,
Ryuhei Akasaka,
Naruhiro Yoshida,
Toru Amaya and
Tetsuo Iwasawa

Full Research Paper
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Beilstein J. Org. Chem. 2022, 18, 963–971, doi:10.3762/bjoc.18.96

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Electroreductive coupling of 2-acylbenzoates with α,β-unsaturated carbonyl compounds: density functional theory study on product selectivity

Naoki Kise and
Toshihiko Sakurai

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Beilstein J. Org. Chem. 2022, 18, 956–962, doi:10.3762/bjoc.18.95

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Introducing a new 7-ring fused diindenone-dithieno[3,2-b:2',3'-d]thiophene unit as a promising component for organic semiconductor materials

Valentin H. K. Fell,
Joseph Cameron,
Alexander L. Kanibolotsky,
Eman J. Hussien and
Peter J. Skabara

Full Research Paper
Published 01 Aug 2022

Beilstein J. Org. Chem. 2022, 18, 944–955, doi:10.3762/bjoc.18.94

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On Reuben G. Jones synthesis of 2-hydroxypyrazines

Pierre Legrand and
Yves L. Janin

Full Research Paper
Published 29 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 935–943, doi:10.3762/bjoc.18.93

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Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

Nisha Devi and
Virender Singh

Full Research Paper
Published 26 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 926–934, doi:10.3762/bjoc.18.92

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Supporting Information File 1: Experimental procedures, characterization data, copies of all ¹H, ¹³C, and ¹⁹F NMR spectra of all new compounds.
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Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine

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Organo-fluorine chemistry III

Latest Articles

Isolation and biosynthesis of daturamycins from Streptomyces sp. KIB-H1544

Automated grindstone chemistry: a simple and facile way for PEG-assisted stoichiometry-controlled halogenation of phenols and anilines using N-halosuccinimides

Molecular diversity of the base-promoted reaction of phenacylmalononitriles with dialkyl but-2-ynedioates

First example of organocatalysis by cathodic N-heterocyclic carbene generation and accumulation using a divided electrochemical flow cell

Understanding the competing pathways leading to hydropyrene and isoelisabethatriene

Electrochemical and spectroscopic properties of twisted dibenzo[g,p]chrysene derivatives

Electroreductive coupling of 2-acylbenzoates with α,β-unsaturated carbonyl compounds: density functional theory study on product selectivity

Introducing a new 7-ring fused diindenone-dithieno[3,2-b:2',3'-d]thiophene unit as a promising component for organic semiconductor materials

On Reuben G. Jones synthesis of 2-hydroxypyrazines

Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

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