Maiti, D. : 2023 Science of Synthesis, 2023/4: Cross-Dehydrogenative Coupling DOI: 10.1055/sos-SD-240-00023
Cross-Dehydrogenative Coupling

6 (Het)Arene/Alkene Cross-Dehydrogenative Coupling for C(sp2)—C(sp2) Bond Formation

Weitere Informationen

Buch

Herausgeber: Maiti, D.

Autoren: Adak, L. ; Ali, W.; Aravindan, N.; Arun, V. ; Baidya, M. ; Besset, T. ; Brocksom, T. J. ; Chen, T. ; Chowdhury, D.; de Oliveira, K. T. ; De Sarkar, S. ; Escudero, J. ; Faisca Phillips, A. M. ; Fukuta, T.; Ghosh, S. ; Ghosh, T.; Guedes da Silva, M. F. C. ; Guin, S.; Han, L.-B. ; Huang, C.-Y. ; Iwasaki, T. ; Jeganmohan, M. ; Jha, N. ; Kakiuchi, F. ; Kambe, N.; Kanai, M. ; Kang, H. ; Kapur, M. ; Khandelia, T. ; Kochi, T. ; Koner, M.; Li, C.; Li, C.-J. ; Li, X. ; Logeswaran, R.; Maes, B. U. W. ; Maiti, D. ; Martins, G. M. ; Miyabe, H. ; Patel, B. K. ; Pombeiro, A. J. L. ; Ranu, B. C. ; Saha, S. K. ; Sambiagio, C. ; Silva, R. C. ; Song, Q. ; Zimmer, G. C.

Titel: Cross-Dehydrogenative Coupling

Print ISBN: 9783132455245; Online ISBN: 9783132455269; Buch-DOI: 10.1055/b000000640

Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie

Science of Synthesis Reference Libraries



Übergeordnete Publikation

Titel: Science of Synthesis

DOI: 10.1055/b-00000101

Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Typ: Mehrbändiges Werk

 


Abstract

The formation of C(sp2)—C(sp2) bonds via the coupling of an aromatic or heteroaromatic species and an alkene is of crucial importance in organic synthesis. While this responsibility has fallen mostly on the Mizoroki–Heck coupling since its discovery half a century ago, the cross-dehydrogenative counterpart, occurring from unfunctionalized reactants, has clear potential advantages in terms of synthetic flexibility and greenness. As cross-dehydrogenative couplings have attracted considerable interest in the recent past, this transformation has been developed from a very limited approach to a much more versatile method. This chapter offers an overview of the different strategies used to functionalize different classes of (hetero)aromatic species, pointing out the strengths and weaknesses of each method.

 
  • 1 Moritani I, Fujiwara Y. Tetrahedron Lett. 1967; 1119
  • 2 Fujiwara Y, Moritani I, Matsuda M, Teranishi S. Tetrahedron Lett. 1968; 3863
  • 8 Shue RS. J. Chem. Soc., Chem. Commun. 1971; 1510
  • 17 Chen H, Farizyan M, van Gemmeren M. Eur. J. Org. Chem. 2020; 6318
  • 45 Álvarez-Casao Y, Fernández-Ibáñez MÁ. Eur. J. Org. Chem. 2019; 1842
  • 49 Sambiagio C, Schönbauer D, Blieck R, Dao-Huy T, Pototschnig G, Schaaf P, Wiesinger T, Zia MF, Wencel-Delord J, Besset T, Maes BUW, Schnürch M. Chem. Soc. Rev. 2018; 47: 6603
  • 52 Capito E, Brown JM, Ricci A. Chem. Commun. (Cambridge) 2005; 1854