A simple and easy to perform synthetic route to functionalized thienyl bicyclo[3.2.1]octadienes

Dragana Vuk,
Irena Škorić,
Valentina Milašinović,
Krešimir Molčanov and
Željko Marinić

Full Research Paper
Published 22 May 2020

Beilstein J. Org. Chem. 2020, 16, 1092–1099, doi:10.3762/bjoc.16.96

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Palladium-catalyzed regio- and stereoselective synthesis of aryl and 3-indolyl-substituted 4-methylene-3,4-dihydroisoquinolin-1(2H)-ones

Valeria Nori,
Antonio Arcadi,
Armando Carlone,
Fabio Marinelli and
Marco Chiarini

Full Research Paper
Published 20 May 2020

Beilstein J. Org. Chem. 2020, 16, 1084–1091, doi:10.3762/bjoc.16.95

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Synthesis and anticancer activity of bis(2-arylimidazo[1,2-a]pyridin-3-yl) selenides and diselenides: the copper-catalyzed tandem C–H selenation of 2-arylimidazo[1,2-a]pyridine with selenium

Mio Matsumura,
Tsutomu Takahashi,
Hikari Yamauchi,
Shunsuke Sakuma,
Yukako Hayashi,
Tadashi Hyodo,
Tohru Obata,
Kentaro Yamaguchi,
Yasuyuki Fujiwara and
Shuji Yasuike

Full Research Paper
Published 20 May 2020

Beilstein J. Org. Chem. 2020, 16, 1075–1083, doi:10.3762/bjoc.16.94

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Synthesis of novel multifunctional carbazole-based molecules and their thermal, electrochemical and optical properties

Nuray Altinolcek,
Ahmet Battal,
Mustafa Tavasli,
William J. Peveler,
Holly A. Yu and
Peter J. Skabara

Full Research Paper
Published 19 May 2020

Beilstein J. Org. Chem. 2020, 16, 1066–1074, doi:10.3762/bjoc.16.93

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Copper-based fluorinated reagents for the synthesis of CF₂R-containing molecules (R ≠ F)

Louise Ruyet and
Tatiana Besset

Review
Published 18 May 2020

Beilstein J. Org. Chem. 2020, 16, 1051–1065, doi:10.3762/bjoc.16.92

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Fluorinated phenylalanines: synthesis and pharmaceutical applications

Laila F. Awad and
Mohammed Salah Ayoup

Review
Published 15 May 2020

Beilstein J. Org. Chem. 2020, 16, 1022–1050, doi:10.3762/bjoc.16.91

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Copper-catalysed alkylation of heterocyclic acceptors with organometallic reagents

Yafei Guo and
Syuzanna R. Harutyunyan

Review
Published 14 May 2020

Beilstein J. Org. Chem. 2020, 16, 1006–1021, doi:10.3762/bjoc.16.90

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Suzuki–Miyaura cross coupling is not an informative reaction to demonstrate the performance of new solvents

James Sherwood

Letter
Published 13 May 2020

Beilstein J. Org. Chem. 2020, 16, 1001–1005, doi:10.3762/bjoc.16.89

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Aryl-substituted acridanes as hosts for TADF-based OLEDs

Naveen Masimukku,
Dalius Gudeika,
Oleksandr Bezvikonnyi,
Ihor Syvorotka,
Rasa Keruckiene,
Dmytro Volyniuk and
Juozas V. Grazulevicius

Full Research Paper
Published 13 May 2020

Beilstein J. Org. Chem. 2020, 16, 989–1000, doi:10.3762/bjoc.16.88

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Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis

Quentin Lefebvre,
Christophe Salomé and
Thomas C. Fessard

Full Research Paper
Published 12 May 2020

Beilstein J. Org. Chem. 2020, 16, 982–988, doi:10.3762/bjoc.16.87

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meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties

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Molecular switches and cages

Latest Articles

A simple and easy to perform synthetic route to functionalized thienyl bicyclo[3.2.1]octadienes

Palladium-catalyzed regio- and stereoselective synthesis of aryl and 3-indolyl-substituted 4-methylene-3,4-dihydroisoquinolin-1(2H)-ones

Synthesis and anticancer activity of bis(2-arylimidazo[1,2-a]pyridin-3-yl) selenides and diselenides: the copper-catalyzed tandem C–H selenation of 2-arylimidazo[1,2-a]pyridine with selenium

Synthesis of novel multifunctional carbazole-based molecules and their thermal, electrochemical and optical properties

Copper-based fluorinated reagents for the synthesis of CF₂R-containing molecules (R ≠ F)

Fluorinated phenylalanines: synthesis and pharmaceutical applications

Copper-catalysed alkylation of heterocyclic acceptors with organometallic reagents

Suzuki–Miyaura cross coupling is not an informative reaction to demonstrate the performance of new solvents

Aryl-substituted acridanes as hosts for TADF-based OLEDs

Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis

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