Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent

Tatsuhiro Uchikura,
Nanami Kamiyama,
Taisuke Ishikawa and
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Letter
Published 30 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2442–2447, doi:10.3762/bjoc.16.198

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Recent developments in enantioselective photocatalysis

Callum Prentice,
James Morrisson,
Andrew D. Smith and
Eli Zysman-Colman

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Beilstein J. Org. Chem. 2020, 16, 2363–2441, doi:10.3762/bjoc.16.197

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A proposed sustainability index for synthesis plans based on input provenance and output fate: application to academic and industrial synthesis plans for vanillin as a case study

John Andraos

Full Research Paper
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Beilstein J. Org. Chem. 2020, 16, 2346–2362, doi:10.3762/bjoc.16.196

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Leonard Himmel,
Oliver Linnenberg,
Elisabeth Isaak and
Markus Albrecht

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Beilstein J. Org. Chem. 2020, 16, 2338–2345, doi:10.3762/bjoc.16.195

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Host–guest interaction of cucurbit[8]uril with oroxin A and its effect on the properties of oroxin A

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Jun Xie,
Guangyan Luo,
Zhu Tao and
Qianjun Zhang

Full Research Paper
Published 22 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2332–2337, doi:10.3762/bjoc.16.194

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Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol

Ekaterina E. Stepanova,
Maksim V. Dmitriev and
Andrey N. Maslivets

Full Research Paper
Published 21 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2322–2331, doi:10.3762/bjoc.16.193

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Design and synthesis of a bis-macrocyclic host and guests as building blocks for small molecular knots

Elizabeth A. Margolis,
Rebecca J. Keyes,
Stephen D. Lockey IV and
Edward E. Fenlon

Full Research Paper
Published 18 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2314–2321, doi:10.3762/bjoc.16.192

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Chan–Evans–Lam N1-(het)arylation and N1-alkеnylation of 4-fluoroalkylpyrimidin-2(1H)-ones

Viktor M. Tkachuk,
Oleh O. Lukianov,
Mykhailo V. Vovk,
Isabelle Gillaizeau and
Volodymyr A. Sukach

Full Research Paper
Published 17 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2304–2313, doi:10.3762/bjoc.16.191

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Formation of an exceptionally stable ketene during phototransformations of bicyclo[2.2.2]oct-5-en-2-ones having mixed chromophores

Asitanga Ghosh

Full Research Paper
Published 15 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2297–2303, doi:10.3762/bjoc.16.190

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Styryl-based new organic chromophores bearing free amino and azomethine groups: synthesis, photophysical, NLO, and thermal properties

Anka Utama Putra,
Deniz Çakmaz,
Nurgül Seferoğlu,
Alberto Barsella and
Zeynel Seferoğlu

Full Research Paper
Published 14 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2282–2296, doi:10.3762/bjoc.16.189

Full Text

Supporting Information File 1: Experimental procedures, product characterization data (mp, NMR, IR, HRMS, [α]_D, HPLC), and spectra (¹H, ¹³C, and ¹⁹F NMR, HPLC).
Format: PDF	Size: 4.2 MB	Download
Supporting Information File 2: Crystallographic details for 12.
Format: CIF	Size: 390.3 KB	Download

Article Citation
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Cited References
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NHC-catalyzed enantioselective synthesis of β-trifluoromethyl-β-hydroxyamides

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Article is part of the issue

Organo-fluorine chemistry V

Latest Articles

Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent

Recent developments in enantioselective photocatalysis

A proposed sustainability index for synthesis plans based on input provenance and output fate: application to academic and industrial synthesis plans for vanillin as a case study

Hierarchically assembled helicates as reaction platform – from stoichiometric Diels–Alder reactions to enamine catalysis

Host–guest interaction of cucurbit[8]uril with oroxin A and its effect on the properties of oroxin A

Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol

Design and synthesis of a bis-macrocyclic host and guests as building blocks for small molecular knots

Chan–Evans–Lam N1-(het)arylation and N1-alkеnylation of 4-fluoroalkylpyrimidin-2(1H)-ones

Formation of an exceptionally stable ketene during phototransformations of bicyclo[2.2.2]oct-5-en-2-ones having mixed chromophores

Styryl-based new organic chromophores bearing free amino and azomethine groups: synthesis, photophysical, NLO, and thermal properties

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