5.1. 13.3 Germylamines (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. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Typ: Mehrbändiges Werk
Abstract

This review describes the synthesis of compounds that have an organogermanium(IV) fragment (R1 3Ge) attached to a formally anionic nitrogen-containing fragment (R2 2N−). It is an update to the earlier Science of Synthesis contribution on these compounds (Section 5.1.13) and covers the literature published since 2003. The synthetic methods described include synthesis by metathesis, ligand exchange, and the oxidative addition of germylenes to different substrates. The synthesis of germylamines using heterocumulenes and the preparation of macrocyclic germylamines is also discussed.
Schlüsselwörter
germylamines - germanes - germanium compounds - macrocyclic ligands - nitrogen ligands - metathesis - halo compounds - lithium compounds- 2 Zaitsev KV, Lam K, Zhanabil Z, Suleimen Y, Kharcheva AV, Tafeenko VA, Oprunenko YF, Poleshchuk OKh, Lermontova EK, Churakov AV. Organometallics 2017; 36: 298
- 3 Amadoruge ML, Yoder CH, Hope Conneywerdy J, Heroux K, Rheingold AL, Weinert CS. Organometallics 2009; 28: 3067
- 4 Schrick EK, Forget TJ, Roewe KD, Schrick AC, Moore CE, Golen JA, Rheingold AL, Materer NF, Weinert CS. Organometallics 2013; 32: 2245
- 9 Shutov PL, Sorokin DA, Karlov SS, Harms K, Oprunenko YF, Churakov AV, Antipin MY, Zaitseva GS, Lorberth J. Organometallics 2003; 22: 516
- 12 Jiménez-Pérez VM, Camacho-Camacho C, Ramos-Organillo Á, Ramírez-Trejo R, Peña-Hueso A, Contreras R, Flores-Parra A. J. Organomet. Chem. 2007; 692: 5549
- 13 Zaitsev KV, Kharcheva AV, Lam K, Zhanabil Z, Issabayeva G, Oprunenko YF, Churakov AV, Zaitseva GS, Karlov SS. J. Organomet. Chem. 2018; 867: 228
- 14 Piskunov AV, Aivaz’yan IA, Poddel’sky AI, Fukin GK, Baranov EV, Cherkasov VK, Abakumov GA. Eur. J. Inorg. Chem. 2008; 1435
- 16 Ghereg D, André E, Gornitzka H, Escudié J, Ouhsaine F, Saffon N, Miqueu K, Sotiropoulos J.-M. Chem.–Eur. J. 2011; 17: 12 763
- 18 Honacker C, Kappelt B, Jabłoński M, Hepp A, Layh M, Rogel F, Uhl W. Eur. J. Inorg. Chem. 2019; 3287
- 19 Nardis S, Mandoj F, Paolesse R, Fronczek FR, Smith KM, Prodi L, Montalti M, Battistini G. Eur. J. Inorg. Chem. 2007; 2345