Published 27 Jul 2020

Beilstein Arch. 2020, 202085. doi:10.3762/bxiv.2020.85.v1

Models of Necessity

  1. Timothy Clark and
  2. 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

  1. Imre Gyűjtő,
  2. Márta Porcs-Makkay,
  3. Ernák Ferenc Várda,
  4. Gyöngyvér Pusztai,
  5. Gábor Tóth,
  6. Gyula Simig and
  7. 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

  1. Lei Hao,
  2. Chao Jie Li,
  3. Lian Bo Zhao,
  4. Xi Xian Xie and
  5. 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

  1. Dalel El-Marrouki,
  2. Sabrina Touchet,
  3. Abderrahmen Abdelli,
  4. Hédi M'Rabet,
  5. Mohamed Lotfi Efrit and
  6. 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

Two-step continuous-flow synthesis of α-terpineol

  1. Beatriz L C de Carvalho,
  2. Anderson R Aguillon,
  3. Raquel A C Leão and
  4. 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

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

  1. Kazuyuki Sato,
  2. Akira Kawasaki,
  3. Yukiko Karuo,
  4. Atsushi Tarui,
  5. Kentaro Kawai and
  6. Masaaki Omote

Published 27 Mar 2020

Beilstein Arch. 2020, 202034. doi:10.3762/bxiv.2020.34.v1

Published 16 Mar 2020

Beilstein Arch. 2020, 202028. doi:10.3762/bxiv.2020.28.v1

Decarboxylative Bromination of Thiazole Core and Consecutive Cross-Coupling Reactions

  1. Emma Freiberger,
  2. Eric Täuscher,
  3. Uwe Ritter,
  4. Nadine Eckert and
  5. Helmar Görls

Published 13 Mar 2020

Beilstein Arch. 2020, 202027. doi:10.3762/bxiv.2020.27.v1

Design, synthesis and biological evaluation of novel 5-bromo derivatives of indole phytoalexins

  1. Mariana Budovská,
  2. Ivana Selešová,
  3. Viera Tischlerová,
  4. Radka Michalková and
  5. Ján Mojžiš

Published 05 Mar 2020

Beilstein Arch. 2020, 202023. doi:10.3762/bxiv.2020.23.v1

Synthesis of aryl 2-bromo-2-chloro-1,1-difluoroethyl ethers mediated by a reaction between phenols and halothane

  1. Yukiko Karuo,
  2. Ayaka Kametani,
  3. Atsushi Tarui,
  4. Kazuyuki Sato,
  5. Kentaro Kawai and
  6. Masaaki Omote

Published 19 Feb 2020

Beilstein Arch. 2020, 202021. doi:10.3762/bxiv.2020.21.v1

Published 17 Feb 2020

Beilstein Arch. 2020, 202020. doi:10.3762/bxiv.2020.20.v1

Published 12 Feb 2020

Beilstein Arch. 2020, 202017. doi:10.3762/bxiv.2020.17.v1

Synthesis and Properties of Tetrathiafulvalenes Bearing 6-Aryl-1,4-dithiafulvenes

  1. Aya Yoshimura,
  2. Hitoshi Kimura,
  3. Kohei Kagawa,
  4. Mayuka Yoshioka,
  5. Toshiki Itou,
  6. Dhananjayan Vasu,
  7. Takashi Shirahata,
  8. Hideki Yorimitsu and
  9. Yohji Misaki

Published 12 Feb 2020

Beilstein Arch. 2020, 202016. doi:10.3762/bxiv.2020.16.v1

Published 07 Feb 2020

Beilstein Arch. 2020, 202015. doi:10.3762/bxiv.2020.15.v1

Copper-Catalyzed Remote C–H Arylation of Polycyclic Aromatic Hydrocarbons (PAHs)

  1. Anping Luo,
  2. Min Zhang,
  3. Zhangyi Fu,
  4. Jingbo Lan,
  5. Di Wu and
  6. Jingsong You

Published 20 Jan 2020

Beilstein Arch. 2020, 202011. doi:10.3762/bxiv.2020.11.v1

Published 14 Jan 2020

Beilstein Arch. 2020, 20208. doi:10.3762/bxiv.2020.8.v1

Published 06 Jan 2020

Beilstein Arch. 2020, 20203. doi:10.3762/bxiv.2020.3.v1

Other Beilstein-Institut Open Science Activities

Logo
Logo
Logo
Symposia