PDF herunterladen
18.15. 8 Tetraheterosubstituted Methanes with a Carbon—Halogen Bond (Update 2018)
Buch
Herausgeber: Banert, K.; Clarke, P. A.; Drabowicz, J.; Oestreich, M.
Titel: Knowledge Updates 2018/4
Print ISBN: 9783132423251; Online ISBN: 9783132423282; Buch-DOI: 10.1055/b-006-161209
1st edition © 2019 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. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Typ: Mehrbändiges Werk
Abstract
In this chapter, recent methods for the preparation and elaboration of various substituted halomethanes are summarized. In addition to updates on classical methods, recently developed procedures employing new fluorinating agents, such as Togni’s reagents, are also presented. These methods are also put in the context of the synthesis of biologically active compounds.
Schlüsselwörter
trifluoromethylation - trifluoromethylsulfanylation - Togni’s reagents - Selectfluor - tetrahalomethanes - Umemoto’s reagent - Ruppert–Prakash reagent - PhenoFluor - trifluoromethylselanylation- 9 Kieltsch I, Eisenberger P, Togni A. Angew. Chem. 2007; 119: 768 Angew. Chem. Int. Ed. 2007; 46: 754
- 11 Koller R, Stanek K, Stolz D, Aardoom R, Niedermann K, Togni A. Angew. Chem. 2009; 121: 4396 Angew. Chem. Int. Ed. 2009; 48: 4332
- 17 Krishanmoorthy S, Schnell SD, Dang H, Fu F, Prakash GKS. J. Fluorine Chem. 2017; 203: 130
Reference Ris Wihthout Link
- 18 Verhoog S, Kee CW, Wang Y, Khotavivattana T, Wilson TC, Kersemans V, Smart S, Tredwell M, Davis BG, Gouverneur V. J. Am. Chem. Soc. 2018; 140: 1572
- 20 Carbonnel E, Besset T, Poisson T, Labar D, Pannecoucke X, Jubault P. Chem. Commun. (Cambridge) 2017; 53: 5706
- 27 Zheng J, Cheng R, Lin J.-H, Yu D.-H, Ma L, Jia L, Zhang L, Wang L, Xiao J.-C, Liang SH. Angew. Chem. 2017; 129: 3244 Angew. Chem. Int. Ed. 2017; 56: 3196
- 30 Danoun G, Bayarmagnai B, Gruenberg MF, Goossen LJ. Chem. Sci. 2014; 5: 1312
Reference Ris Wihthout Link
- 36 Park C.-M, Bruncko M, Adickes J, Bauch J, Ding H, Kunzer A, Marsh KC, Nimmer P, Shoemaker AR, Song X, Tahir SK, Tse C, Wang X, Wendt MD, Yang X, Zhang H, Fesik SW, Rosenberg SH, Elmore SW. J. Med. Chem. 2008; 51: 6902
- 38 Dubbaka SR, Atthunuri AR, Prakash KC, Rangabashyam P, Gadde S, Kothandaraman R. Synthesis 2016; 48: 1246
- 40 Chen C, Xie Y, Chu L, Wang R.-W, Zhang X, Qing F.-L. Angew. Chem. 2012; 124: 2542 Angew. Chem. Int. Ed. 2012; 51: 2492
- 42 Gutmann B, Obermayer D, Reichart B, Prekodravac B, Irfan M, Kremsner JM, Kappe CO. Chem.–Eur. J. 2010; 16: 12 182
- 44 Khotavivattana T, Verhoog S, Tredwell M, Pfeifer L, Calderwood S, Wheelhouse K, Collier TL, Gouverneur V. Angew. Chem. 2015; 127: 10 129 Angew. Chem. Int. Ed. 2015; 54: 9991
- 49 Lishchynskyi A, Novikov MA, Martin E, Escudero-Adán EC, Novák P, Grushin VV. J. Org. Chem. 2013; 78: 11 126
- 55 Scattolin T, Deckers K, Schoenebeck F. Angew. Chem. 2017; 129: 227 Angew. Chem. Int. Ed. 2017; 56: 221
- 56 Niedermann K, Früh N, Vinogradova E, Wiehn MS, Moreno A, Togni A. Angew. Chem. 2011; 123: 1091 Angew. Chem. Int. Ed. 2011; 50: 1059