14.5. 3 3-Oxidopyrylium Salts and Their Thio and Benzo-Fused Analogues (Update 2020)
Buch
Herausgeber: Jiang, X.; Marschner, C.; Oestreich, M.; Wang, M.
Titel: Knowledge Updates 2020/3
Print ISBN: 9783132435643; Online ISBN: 9783132435667; Buch-DOI: 10.1055/b000000104
1st edition © 2020 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Knowledge Updates
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.; Nevado, C.; Trost, B. M.; You, S.
Typ: Mehrbändiges Werk
Abstract
This chapter is an update to the earlier Science of Synthesis contribution (Section 14.5) describing methods for the synthesis of 3-oxidopyrylium salts and their thio and benzo-fused analogues. It focuses on the literature published in the period 2004–2019.
Schlüsselwörter
3-oxidopyrylium salts - benzofurans - benzothiophenes - anthocyanidins - cyclization - condensation-
1 Tolkunov S. V., Tolkunov V. S., Dulenko V. I.. Chem. Heterocycl. Compd. (Engl. Transl.) 2004; 40: 481
-
2 Tolkunov S. V., Khyzhan A. I., Suikov S. Y., Dulenko V. I.. Chem. Heterocycl. Compd. (Engl. Transl.) 2005; 41: 379
-
9 Tennakone K., Kumara G. R. R. A., Kumarasinghe A. R., Wijayantha K. G. U., Sirimanne P. M.. Semicond. Sci. Technol 1995; 10: 1689
-
10 Calogero G., Sinopoli A., Citro I., Di Marco G., Petrov V., Diniz A. M., Parola A. J., Pina F.. Photochem. Photobiol. Sci 2013; 12: 883
- 17 Stark A., Seddon K. R., Kirk-Othmer Encyclopedia of Chemical Technology. Seidel A.. Wiley; Hoboken 2007. 26, pp 836–920.
-
21 Pernak J., Świerczyńska A., Kot M., Walkiewicz F., Maciejewski H.. Tetrahedron Lett 2011; 52: 4342
-
24 Hirsch D. R., Schiavone D. V., Berkowitz A. J., Morrison L. A., Masaoka T., Wilson J. A., Lomonosova E., Zhao H., Patel B. S., Datla S. H., Hoft S. G., Majidi S. J., Pal R. K., Gallicchio E., Tang L., Tavis J. E., Le Grice S. F. J., Beutler J. A., Murelli R. P.. Org. Biomol. Chem 2018; 16: 62