A new glance at the chemosphere of macroalgal–bacterial interactions: In situ profiling of metabolites in symbiosis by mass spectrometry
- Marine Vallet,
- Filip Kaftan,
- Veit Grabe,
- Fatemeh Ghaderiardakani,
- Simona Fenizia,
- Aleš Svatoš,
- Georg Pohnert and
- Thomas Wichard
Beilstein J. Org. Chem. 2021, 17, 1313–1322, doi:10.3762/bjoc.17.91
Photoinduced post-modification of graphitic carbon nitride-embedded hydrogels: synthesis of 'hydrophobic hydrogels' and pore substructuring
- Cansu Esen and
- Baris Kumru
Beilstein J. Org. Chem. 2021, 17, 1323–1334, doi:10.3762/bjoc.17.92
Icilio Guareschi and his amazing “1897 reaction”
- Gian Cesare Tron,
- Alberto Minassi,
- Giovanni Sorba,
- Mara Fausone and
- Giovanni Appendino
Beilstein J. Org. Chem. 2021, 17, 1335–1351, doi:10.3762/bjoc.17.93
Fritsch–Buttenberg–Wiechell rearrangement of magnesium alkylidene carbenoids leading to the formation of alkynes
- Tsutomu Kimura,
- Koto Sekiguchi,
- Akane Ando and
- Aki Imafuji
Beilstein J. Org. Chem. 2021, 17, 1352–1359, doi:10.3762/bjoc.17.94
Antiviral therapy in shrimp through plant virus VLP containing VP28 dsRNA against WSSV
- Santiago Ramos-Carreño,
- Ivone Giffard-Mena,
- Jose N. Zamudio-Ocadiz,
- Alfredo Nuñez-Rivera,
- Ricardo Valencia-Yañez,
- Jaime Ruiz-Garcia,
- Maria Teresa Viana and
- Ruben D. Cadena-Nava
Beilstein J. Org. Chem. 2021, 17, 1360–1373, doi:10.3762/bjoc.17.95
Design, synthesis and photophysical properties of novel star-shaped truxene-based heterocycles utilizing ring-closing metathesis, Clauson–Kaas, Van Leusen and Ullmann-type reactions as key tools
- Shakeel Alvi and
- Rashid Ali
Beilstein J. Org. Chem. 2021, 17, 1374–1384, doi:10.3762/bjoc.17.96
Analogs of the carotane antibiotic fulvoferruginin from submerged cultures of a Thai Marasmius sp.
- Birthe Sandargo,
- Leon Kaysan,
- Rémy B. Teponno,
- Christian Richter,
- Benjarong Thongbai,
- Frank Surup and
- Marc Stadler
Beilstein J. Org. Chem. 2021, 17, 1385–1391, doi:10.3762/bjoc.17.97
Double-headed nucleosides: Synthesis and applications
- Vineet Verma,
- Jyotirmoy Maity,
- Vipin K. Maikhuri,
- Ritika Sharma,
- Himal K. Ganguly and
- Ashok K. Prasad
Beilstein J. Org. Chem. 2021, 17, 1392–1439, doi:10.3762/bjoc.17.98
Total synthesis of ent-pavettamine
- Memory Zimuwandeyi,
- Manuel A. Fernandes,
- Amanda L. Rousseau and
- Moira L. Bode
Beilstein J. Org. Chem. 2021, 17, 1440–1446, doi:10.3762/bjoc.17.99
Organocatalytic asymmetric Michael/acyl transfer reaction between α-nitroketones and 4-arylidenepyrrolidine-2,3-diones
- Chandrakanta Parida and
- Subhas Chandra Pan
Beilstein J. Org. Chem. 2021, 17, 1447–1452, doi:10.3762/bjoc.17.100
Synthesis of 1-indolyl-3,5,8-substituted γ-carbolines: one-pot solvent-free protocol and biological evaluation
- Premansh Dudhe,
- Mena Asha Krishnan,
- Kratika Yadav,
- Diptendu Roy,
- Krishnan Venkatasubbaiah,
- Biswarup Pathak and
- Venkatesh Chelvam
Beilstein J. Org. Chem. 2021, 17, 1453–1463, doi:10.3762/bjoc.17.101
Iodine-catalyzed electrophilic substitution of indoles: Synthesis of (un)symmetrical diindolylmethanes with a quaternary carbon center
- Thanigaimalai Pillaiyar,
- Masoud Sedaghati,
- Andhika B. Mahardhika,
- Lukas L. Wendt and
- Christa E. Müller
Beilstein J. Org. Chem. 2021, 17, 1464–1475, doi:10.3762/bjoc.17.102
Co-crystallization of an organic solid and a tetraaryladamantane at room temperature
- Fabian Rami,
- Jan Nowak,
- Felix Krupp,
- Wolfgang Frey and
- Clemens Richert
Beilstein J. Org. Chem. 2021, 17, 1476–1480, doi:10.3762/bjoc.17.103
Cascade intramolecular Prins/Friedel–Crafts cyclization for the synthesis of 4-aryltetralin-2-ols and 5-aryltetrahydro-5H-benzo[7]annulen-7-ols
- Jie Zheng,
- Shuyu Meng and
- Quanrui Wang
Beilstein J. Org. Chem. 2021, 17, 1481–1489, doi:10.3762/bjoc.17.104
Free-radical cyclization approach to polyheterocycles containing pyrrole and pyridine rings
- Ivan P. Mosiagin,
- Olesya A. Tomashenko,
- Dar’ya V. Spiridonova,
- Mikhail S. Novikov,
- Sergey P. Tunik and
- Alexander F. Khlebnikov
Beilstein J. Org. Chem. 2021, 17, 1490–1498, doi:10.3762/bjoc.17.105
One-step synthesis of imidazoles from Asmic (anisylsulfanylmethyl isocyanide)
- Louis G. Mueller,
- Allen Chao,
- Embarek AlWedi and
- Fraser F. Fleming
Beilstein J. Org. Chem. 2021, 17, 1499–1502, doi:10.3762/bjoc.17.106
