Photoswitches beyond azobenzene: a beginner’s guide
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Beilstein J. Org. Chem. 2025, 21, 1808–1853, doi:10.3762/bjoc.21.143
Systematic pore lipophilization to enhance the efficiency of an amine-based MOF catalyst in the solvent-free Knoevenagel reaction
- Pricilla Matseketsa,
- Margret Kumbirayi Ruwimbo Pagare and
- Tendai Gadzikwa
Beilstein J. Org. Chem. 2025, 21, 1854–1863, doi:10.3762/bjoc.21.144
Chiral phosphoric acid-catalyzed asymmetric synthesis of helically chiral, planarly chiral and inherently chiral molecules
- Wei Liu and
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Beilstein J. Org. Chem. 2025, 21, 1864–1889, doi:10.3762/bjoc.21.145
Preparation of spirocyclic oxindoles by cyclisation of an oxime to a nitrone and dipolar cycloaddition
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Beilstein J. Org. Chem. 2025, 21, 1890–1896, doi:10.3762/bjoc.21.146
Stereoselective electrochemical intramolecular imino-pinacol reaction: a straightforward entry to enantiopure piperazines
- Margherita Gazzotti,
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- Valerio Chiroli,
- Laura Raimondi,
- Sergio Rossi and
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Beilstein J. Org. Chem. 2025, 21, 1897–1908, doi:10.3762/bjoc.21.147
Synthesis, biological and electrochemical evaluation of glycidyl esters of phosphorus acids as potential anticancer drugs
- Almaz A. Zagidullin,
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Beilstein J. Org. Chem. 2025, 21, 1909–1916, doi:10.3762/bjoc.21.148
Synthesis of N-doped chiral macrocycles by regioselective palladium-catalyzed arylation
- Shuhai Qiu and
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Beilstein J. Org. Chem. 2025, 21, 1917–1923, doi:10.3762/bjoc.21.149
Rhodium-catalysed connective synthesis of diverse reactive probes bearing S(VI) electrophilic warheads
- Scott Rice,
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- Megan H. Wright,
- Stephen P. Marsden,
- Terry K. Smith and
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Beilstein J. Org. Chem. 2025, 21, 1924–1931, doi:10.3762/bjoc.21.150
Enantioselective desymmetrization strategy of prochiral 1,3-diols in natural product synthesis
- Lihua Wei,
- Rui Yang,
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Beilstein J. Org. Chem. 2025, 21, 1932–1963, doi:10.3762/bjoc.21.151
Asymmetric total synthesis of tricyclic prostaglandin D2 metabolite methyl ester via oxidative radical cyclization
- Miao Xiao,
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- Qiaoli Shang,
- Lei Zhu and
- Jun Huang
Beilstein J. Org. Chem. 2025, 21, 1964–1972, doi:10.3762/bjoc.21.152
Photochemical reduction of acylimidazolium salts
- Michael Jakob,
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- Janos Wasternack,
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Beilstein J. Org. Chem. 2025, 21, 1973–1983, doi:10.3762/bjoc.21.153
Aryl iodane-induced cascade arylation–1,2-silyl shift–heterocyclization of propargylsilanes under copper catalysis
- Rasma Kroņkalne,
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- Armands Sebris,
- Anatoly Mishnev and
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Beilstein J. Org. Chem. 2025, 21, 1984–1994, doi:10.3762/bjoc.21.154
Measuring the stereogenic remoteness in non-central chirality: a stereocontrol connectivity index for asymmetric reactions
- Ivan Keng Wee On,
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- Sambhav Baid and
- Ye Zhu
Beilstein J. Org. Chem. 2025, 21, 1995–2006, doi:10.3762/bjoc.21.155
Understanding the origin of stereoselectivity in the photochemical denitrogenation of 2,3-diazabicyclo[2.2.1]heptene and its derivatives with non-adiabatic molecular dynamics
- Leticia A. Gomes and
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Beilstein J. Org. Chem. 2025, 21, 2007–2020, doi:10.3762/bjoc.21.156
α-Ketoglutaric acid in Ugi reactions and Ugi/aza-Wittig tandem reactions
- Vladyslav O. Honcharov,
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- Olena H. Shvets,
- Vyacheslav E. Saraev,
- Svitlana V. Shishkina,
- Tetyana V. Shcherbakova and
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Beilstein J. Org. Chem. 2025, 21, 2021–2029, doi:10.3762/bjoc.21.157
Switchable pathways of multicomponent heterocyclizations of 5-amino-1,2,4-triazoles with salicylaldehydes and pyruvic acid
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- Oleksander V. Buravov,
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- Anastasia Yu. Andryushchenko,
- Svitlana V. Shishkina and
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Beilstein J. Org. Chem. 2025, 21, 2030–2035, doi:10.3762/bjoc.21.158
Solar thermal fuels: azobenzene as a cyclic photon–heat transduction platform
- Jie Yan,
- Shaodong Sun,
- Minghao Wang and
- Si Wu
Beilstein J. Org. Chem. 2025, 21, 2036–2047, doi:10.3762/bjoc.21.159
Bioinspired total syntheses of natural products: a personal adventure
- Zhengyi Qin,
- Yuting Yang,
- Nuran Yan,
- Xinyu Liang,
- Zhiyu Zhang,
- Yaxuan Duan,
- Huilin Li and
- Xuegong She
Beilstein J. Org. Chem. 2025, 21, 2048–2061, doi:10.3762/bjoc.21.160
Discovery of cytotoxic indolo[1,2-c]quinazoline derivatives through scaffold-based design
- Daniil V. Khabarov,
- Valeria A. Litvinova,
- Lyubov G. Dezhenkova,
- Dmitry N. Kaluzhny,
- Alexander S. Tikhomirov and
- Andrey E. Shchekotikhin
Beilstein J. Org. Chem. 2025, 21, 2062–2071, doi:10.3762/bjoc.21.161
Further elaboration of the stereodivergent approach to chaetominine-type alkaloids: synthesis of the reported structures of aspera chaetominines A and B and revised structure of aspera chaetominine B
- Jin-Fang Lü,
- Jiang-Feng Wu,
- Jian-Liang Ye and
- Pei-Qiang Huang
Beilstein J. Org. Chem. 2025, 21, 2072–2081, doi:10.3762/bjoc.21.162
Multicomponent reactions IV
- Thomas J. J. Müller and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2025, 21, 2082–2084, doi:10.3762/bjoc.21.163
The application of desymmetric enantioselective reduction of cyclic 1,3-dicarbonyl compounds in the total synthesis of terpenoid and alkaloid natural products
- Dong-Xing Tan and
- Fu-She Han
Beilstein J. Org. Chem. 2025, 21, 2085–2102, doi:10.3762/bjoc.21.164
