Hydrazides in the reaction with hydroxypyrrolines: less nucleophilicity – more diversity
- Dmitrii A. Shabalin,
- Evgeniya E. Ivanova,
- Igor A. Ushakov,
- Elena Yu. Schmidt and
- Boris A. Trofimov
Beilstein J. Org. Chem. 2021, 17, 319–324, doi:10.3762/bjoc.17.29
Regioselective chemoenzymatic syntheses of ferulate conjugates as chromogenic substrates for feruloyl esterases
- Olga Gherbovet,
- Fernando Ferreira,
- Apolline Clément,
- Mélanie Ragon,
- Julien Durand,
- Sophie Bozonnet,
- Michael J. O'Donohue and
- Régis Fauré
Beilstein J. Org. Chem. 2021, 17, 325–333, doi:10.3762/bjoc.17.30
Synthesis of legonmycins A and B, C(7a)-hydroxylated bacterial pyrrolizidines
- Wilfred J. M. Lewis,
- David M. Shaw and
- Jeremy Robertson
Beilstein J. Org. Chem. 2021, 17, 334–342, doi:10.3762/bjoc.17.31
CF3-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
- Anthony J. Fernandes,
- Armen Panossian,
- Bastien Michelet,
- Agnès Martin-Mingot,
- Frédéric R. Leroux and
- Sébastien Thibaudeau
Beilstein J. Org. Chem. 2021, 17, 343–378, doi:10.3762/bjoc.17.32
Coupling biocatalysis with high-energy flow reactions for the synthesis of carbamates and β-amino acid derivatives
- Alexander Leslie,
- Thomas S. Moody,
- Megan Smyth,
- Scott Wharry and
- Marcus Baumann
Beilstein J. Org. Chem. 2021, 17, 379–384, doi:10.3762/bjoc.17.33
Mesoionic tetrazolium-5-aminides: Synthesis, molecular and crystal structures, UV–vis spectra, and DFT calculations
- Vladislav A. Budevich,
- Sergei V. Voitekhovich,
- Alexander V. Zuraev,
- Vadim E. Matulis,
- Vitaly E. Matulis,
- Alexander S. Lyakhov,
- Ludmila S. Ivashkevich and
- Oleg A. Ivashkevich
Beilstein J. Org. Chem. 2021, 17, 385–395, doi:10.3762/bjoc.17.34
Helicene synthesis by Brønsted acid-catalyzed cycloaromatization in HFIP [(CF3)2CHOH]
- Takeshi Fujita,
- Noriaki Shoji,
- Nao Yoshikawa and
- Junji Ichikawa
Beilstein J. Org. Chem. 2021, 17, 396–403, doi:10.3762/bjoc.17.35
Unexpected rearrangements and a novel synthesis of 1,1-dichloro-1-alkenones from 1,1,1-trifluoroalkanones with aluminium trichloride
- Beatrice Lansbergen,
- Catherine S. Meister and
- Michael C. McLeod
Beilstein J. Org. Chem. 2021, 17, 404–409, doi:10.3762/bjoc.17.36
1,2,3-Triazoles as leaving groups: SNAr reactions of 2,6-bistriazolylpurines with O- and C-nucleophiles
- Dace Cīrule,
- Irina Novosjolova,
- Ērika Bizdēna and
- Māris Turks
Beilstein J. Org. Chem. 2021, 17, 410–419, doi:10.3762/bjoc.17.37
Identification of volatiles from six marine Celeribacter strains
- Anuj Kumar Chhalodia,
- Jan Rinkel,
- Dorota Konvalinkova,
- Jörn Petersen and
- Jeroen S. Dickschat
Beilstein J. Org. Chem. 2021, 17, 420–430, doi:10.3762/bjoc.17.38
Synthesis of trifluoromethyl ketones by nucleophilic trifluoromethylation of esters under a fluoroform/KHMDS/triglyme system
- Yamato Fujihira,
- Yumeng Liang,
- Makoto Ono,
- Kazuki Hirano,
- Takumi Kagawa and
- Norio Shibata
Beilstein J. Org. Chem. 2021, 17, 431–438, doi:10.3762/bjoc.17.39
Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement
- Vladimir Kubyshkin,
- Rebecca Davis and
- Nediljko Budisa
Beilstein J. Org. Chem. 2021, 17, 439–460, doi:10.3762/bjoc.17.40
Synthetic strategies of phosphonodepsipeptides
- Jiaxi Xu
Beilstein J. Org. Chem. 2021, 17, 461–484, doi:10.3762/bjoc.17.41
Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines
- Geetanjali S. Sontakke,
- Rahul K. Shukla and
- Chandra M. R. Volla
Beilstein J. Org. Chem. 2021, 17, 485–493, doi:10.3762/bjoc.17.42
The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst
- Deniz Tözendemir and
- Cihangir Tanyeli
Beilstein J. Org. Chem. 2021, 17, 494–503, doi:10.3762/bjoc.17.43
Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes
- Olga Bakhanovich,
- Viktor Khutorianskyi,
- Vladimir Motornov and
- Petr Beier
Beilstein J. Org. Chem. 2021, 17, 504–510, doi:10.3762/bjoc.17.44
Synthesis and physicochemical evaluation of fluorinated lipopeptide precursors of ligands for microbubble targeting
- Masayori Hagimori,
- Estefanía E. Mendoza-Ortega and
- Marie Pierre Krafft
Beilstein J. Org. Chem. 2021, 17, 511–518, doi:10.3762/bjoc.17.45
A new and efficient methodology for olefin epoxidation catalyzed by supported cobalt nanoparticles
- Lucía Rossi-Fernández,
- Viviana Dorn and
- Gabriel Radivoy
Beilstein J. Org. Chem. 2021, 17, 519–526, doi:10.3762/bjoc.17.46
Synthesis of (Z)-3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones using an Eschenmoser coupling reaction
- Lukáš Marek,
- Lukáš Kolman,
- Jiří Váňa,
- Jan Svoboda and
- Jiří Hanusek
Beilstein J. Org. Chem. 2021, 17, 527–539, doi:10.3762/bjoc.17.47
Menthyl esterification allows chiral resolution for the synthesis of artificial glutamate analogs
- Kenji Morokuma,
- Shuntaro Tsukamoto,
- Kyosuke Mori,
- Kei Miyako,
- Ryuichi Sakai,
- Raku Irie and
- Masato Oikawa
Beilstein J. Org. Chem. 2021, 17, 540–550, doi:10.3762/bjoc.17.48
Metal-free visible-light-enabled vicinal trifluoromethyl dithiolation of unactivated alkenes
- Xiaojuan Li,
- Qiang Zhang,
- Weigang Zhang,
- Jinzhu Ma,
- Yi Wang and
- Yi Pan
Beilstein J. Org. Chem. 2021, 17, 551–557, doi:10.3762/bjoc.17.49
Amino- and polyaminophthalazin-1(2H)-ones: synthesis, coordination properties, and biological activity
- Zbigniew Malinowski,
- Emilia Fornal,
- Agata Sumara,
- Renata Kontek,
- Karol Bukowski,
- Beata Pasternak,
- Dariusz Sroczyński,
- Joachim Kusz,
- Magdalena Małecka and
- Monika Nowak
Beilstein J. Org. Chem. 2021, 17, 558–568, doi:10.3762/bjoc.17.50
Breakdown of 3-(allylsulfonio)propanoates in bacteria from the Roseobacter group yields garlic oil constituents
- Anuj Kumar Chhalodia and
- Jeroen S. Dickschat
Beilstein J. Org. Chem. 2021, 17, 569–580, doi:10.3762/bjoc.17.51
Designed whole-cell-catalysis-assisted synthesis of 9,11-secosterols
- Marek Kõllo,
- Marje Kasari,
- Villu Kasari,
- Tõnis Pehk,
- Ivar Järving,
- Margus Lopp,
- Arvi Jõers and
- Tõnis Kanger
Beilstein J. Org. Chem. 2021, 17, 581–588, doi:10.3762/bjoc.17.52
Valorisation of plastic waste via metal-catalysed depolymerisation
- Francesca Liguori,
- Carmen Moreno-Marrodán and
- Pierluigi Barbaro
Beilstein J. Org. Chem. 2021, 17, 589–621, doi:10.3762/bjoc.17.53
