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
Published 22 Oct 2020
Beilstein Arch. 2020, 2020122. doi:10.3762/bxiv.2020.122.v1
Published 12 Oct 2020
Beilstein Arch. 2020, 2020118. doi:10.3762/bxiv.2020.118.v1

Metal-free synthesis of biarenes via photoextrusion in di(tri)arylphosphates

  • Hisham Qrareya,
  • Lorenzo Meazza,
  • Stefano Protti and
  • Maurizio Fagnoni
Published 28 Sep 2020
Beilstein Arch. 2020, 2020110. doi:10.3762/bxiv.2020.110.v1
Published 25 Aug 2020
Beilstein Arch. 2020, 202096. doi:10.3762/bxiv.2020.96.v1
Published 25 Aug 2020
Beilstein Arch. 2020, 202094. doi:10.3762/bxiv.2020.94.v1
Published 27 Jul 2020
Beilstein Arch. 2020, 202085. doi:10.3762/bxiv.2020.85.v1

Models of Necessity

  • Timothy Clark and
  • Martin G Hicks
Published 19 Jun 2020
Beilstein Arch. 2020, 202077. doi:10.3762/bxiv.2020.77.v1

Transformation of 2H-1,2,3-benzothiadiazine 1,1-dioxides variously substituted at the aromatic ring, via nucleophilic substitution and demethylation reactions

  • Imre Gyűjtő,
  • Márta Porcs-Makkay,
  • Ernák Ferenc Várda,
  • Gyöngyvér Pusztai,
  • Gábor Tóth,
  • Gyula Simig and
  • Balázs Volk
Published 16 Jun 2020
Beilstein Arch. 2020, 202073. doi:10.3762/bxiv.2020.73.v1
Published 10 Jun 2020
Beilstein Arch. 2020, 202071. doi:10.3762/bxiv.2020.71.v1
Published 22 May 2020
Beilstein Arch. 2020, 202063. doi:10.3762/bxiv.2020.63.v1

A Novel Sustainable Method to Prepare Glutaric Acid from Glucose

  • Lei Hao,
  • Chao Jie Li,
  • Lian Bo Zhao,
  • Xi Xian Xie and
  • Kui Lu
Published 19 May 2020
Beilstein Arch. 2020, 202062. doi:10.3762/bxiv.2020.62.v1
Published 08 May 2020
Beilstein Arch. 2020, 202060. doi:10.3762/bxiv.2020.60.v1
Published 05 May 2020
Beilstein Arch. 2020, 202057. doi:10.3762/bxiv.2020.57.v1

Tuneable access to indole, indolone and cinnoline derivatives from a common 1,4-diketone Michael acceptor

  • Dalel El-Marrouki,
  • Sabrina Touchet,
  • Abderrahmen Abdelli,
  • Hédi M'Rabet,
  • Mohamed Lotfi Efrit and
  • Philippe C. Gros
Published 27 Apr 2020
Beilstein Arch. 2020, 202056. doi:10.3762/bxiv.2020.56.v1
Published 27 Apr 2020
Beilstein Arch. 2020, 202055. doi:10.3762/bxiv.2020.55.v1
Published 21 Apr 2020
Beilstein Arch. 2020, 202053. doi:10.3762/bxiv.2020.53.v1
Published 20 Apr 2020
Beilstein Arch. 2020, 202052. doi:10.3762/bxiv.2020.52.v1

Microwave-assisted efficient one-pot synthesis of N2-(tetrazol-5-yl)-6-aryl/heteroaryl-2,3-dihydro-1,3,5-triazine-2,4-diamines

  • Moustafa Moustafa,
  • Ramadan Mekheimer,
  • Saleh Al-Mousawi,
  • Mohamed Abd-Elmonem,
  • Hesham El-Zorba,
  • Afaf Abdel Hameed,
  • Tahany Mohamed and
  • Kamal Usef Sadek
Published 16 Apr 2020
Beilstein Arch. 2020, 202051. doi:10.3762/bxiv.2020.51.v1
Published 14 Apr 2020
Beilstein Arch. 2020, 202049. doi:10.3762/bxiv.2020.49.v1
Published 06 Apr 2020
Beilstein Arch. 2020, 202043. doi:10.3762/bxiv.2020.43.v1

Two-step continuous-flow synthesis of α-terpineol

  • Beatriz L C de Carvalho,
  • Anderson R Aguillon,
  • Raquel A C Leão and
  • Rodrigo Octavio M. A. de Souza
Published 06 Apr 2020
Beilstein Arch. 2020, 202041. doi:10.3762/bxiv.2020.41.v1
Published 06 Apr 2020
Beilstein Arch. 2020, 202040. doi:10.3762/bxiv.2020.40.v1
Published 01 Apr 2020
Beilstein Arch. 2020, 202038. doi:10.3762/bxiv.2020.38.v1

Distinctive Reactivity of N-benzylidene-[1,1'-biphenyl]-2-amines under Photoredox Catalysis

  • Shrikant Tambe,
  • Kwan Hong Min,
  • Naeem Iqbal and
  • Eun Jin Cho
Published 30 Mar 2020
Beilstein Arch. 2020, 202035. doi:10.3762/bxiv.2020.35.v1

Synthesis of new fluorescent molecules having an aggregation-induced emission property derived from 4-fluoroisoxazoles

  • Kazuyuki Sato,
  • Akira Kawasaki,
  • Yukiko Karuo,
  • Atsushi Tarui,
  • Kentaro Kawai and
  • Masaaki Omote
Published 27 Mar 2020
Beilstein Arch. 2020, 202034. doi:10.3762/bxiv.2020.34.v1
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