Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 2008, 73, 1814-1824
https://doi.org/10.1135/cccc20081814

Use of Cyclic α,β-Unsaturated Trifluoromethyl Sulfones in Diels-Alder Reactions and Michael Additions

Thierry Billarda,*, Bernard R. Langloisa, Michael Essersb and Günter Haufeb,*

a ICBMS, Institut de Chimie et Biochimie Moléculaires et Supramoléculaires, Equipe SERCOF, 43 boulevard du 11 novembre 1918, Villeurbanne, F-69622, France; CNRS, UMR5246, Villeurbanne, F-69622, France; Université de Lyon, Lyon, F-69622, France; Université Lyon 1, Lyon, F-69622, France; INSA-Lyon, Villeurbanne, F-69622, France; CPE Lyon, Villeurbanne, F-69616, France
b Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Correnstrasse 40, D-48149 Münster, Germany

Crossref Cited-by Linking

  • Huang Xin, Besset Tatiana, Jubault Philippe, Couve‐Bonnaire Samuel: Fluorinated Substrates as Michael Acceptors Towards Fine Chemicals. Adv Synth Catal 2023, 365, 2467. <https://doi.org/10.1002/adsc.202300565>
  • Essers Michael, Haufe Günter: Synthesis of Diastereomeric 8‐Fluoro‐ABC‐Steroid Building Blocks. Eur J Org Chem 2023, 26. <https://doi.org/10.1002/ejoc.202300206>
  • Haufe Günter: Selective Synthesis of Monofluorinated Compounds Applying Amine/HF Reagents. The Chemical Record 2023, 23. <https://doi.org/10.1002/tcr.202300140>
  • Sokolenko Liubov V., Rusanov Eduard B., Yagupolskii Yurii L.: CF3S(O)n-Containing olefins in cyclopropanation reactions. Journal of Fluorine Chemistry 2021, 248, 109802. <https://doi.org/10.1016/j.jfluchem.2021.109802>
  • Kondratov Ivan S., Tolmachova Nataliya A., Haufe Günter: Diels–Alder Reaction in the Synthesis of Fluorinated (Hetero)Aromatic Compounds. Eur J Org Chem 2018, 2018, 3618. <https://doi.org/10.1002/ejoc.201800327>
  • Ramb Daniel C., Lerchen Andreas, Kischkewitz Marvin, Beutel Bernd, Fustero Santos, Haufe Günter: Addition of Nucleophiles to Fluorinated Michael Acceptors. Eur J Org Chem 2016, 2016, 1751. <https://doi.org/10.1002/ejoc.201600088>
  • Xu Xiu-Hua, Matsuzaki Kohei, Shibata Norio: Synthetic Methods for Compounds Having CF3–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions. Chem. Rev. 2015, 115, 731. <https://doi.org/10.1021/cr500193b>
  • Kondratov Ivan S., Tolmachova Nataliya A., Dolovanyuk Violetta G., Gerus Igor I., Bergander Klaus, Daniliuc Constantin‐Gabriel, Haufe Günter: Diels–Alder Reaction of Ethyl 3‐Benzamido‐2‐oxo‐6‐(trifluoromethyl)‐2H‐pyran‐5‐carboxylate with Alkoxyalkenes as an Effective Approach to Trifluoromethyl‐Containing 3‐Aminobenzoic Acid Derivatives. Eur J Org Chem 2014, 2014, 2443. <https://doi.org/10.1002/ejoc.201301485>
  • Xu Xiu‐Hua, Taniguchi Misaki, Wang Xin, Tokunaga Etsuko, Ozawa Tomohiro, Masuda Hideki, Shibata Norio: Stereoselective Synthesis of Vinyl Triflones and Heteroaryl Triflones through Anionic O→Cvinyl and N→Cvinyl Trifluoromethanesulfonyl Migration Reactions. Angewandte Chemie 2013, 125, 12860. <https://doi.org/10.1002/ange.201307535>
  • Xu Xiu‐Hua, Taniguchi Misaki, Wang Xin, Tokunaga Etsuko, Ozawa Tomohiro, Masuda Hideki, Shibata Norio: Stereoselective Synthesis of Vinyl Triflones and Heteroaryl Triflones through Anionic O→Cvinyl and N→Cvinyl Trifluoromethanesulfonyl Migration Reactions. Angew Chem Int Ed 2013, 52, 12628. <https://doi.org/10.1002/anie.201307535>
  • Billard Thierry, Langlois Bernard R., Essers Michael, Haufe Guenter: ChemInform Abstract: Use of Cyclic α,β‐Unsaturated Trifluoromethyl Sulfones in Diels—Alder Reactions and Michael Additions. ChemInform 2009, 40. <https://doi.org/10.1002/chin.200921026>