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

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Ying Han,
Jing Sun and
Chao-Guo Yan

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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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Ana A. Folgueiras-Amador,
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

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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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Published 02 Aug 2022

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

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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

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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

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Published 26 Jul 2022

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

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Coupling biocatalysis with high-energy flow reactions for the synthesis of carbamates and β-amino acid derivatives

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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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