Bis(trimethylsilyl)amid lithný (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Bis(trimethylsilyl)amid lithný" in Czech language version.

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9doi.org

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archive.org

Michael Lappert; Andrey Protchenko; Philip Power; Alexandra Seeber. Metal Amide Chemistry. Weinheim: Wiley-VCH, 2009. Dostupné online. doi:10.1002/9780470740385. S. 196–199.

doi.org

E. H. Amonoo-Neizer; R. A. Shaw; D. O. Skovlin; B. C. Smith. Lithium Bis(Trimethylsilyl)Amide and Tris(Trimethylsilyl)Amine. Inorganic Syntheses. 1966, s. 19–22. ISBN 978-0-470-13239-5. doi:10.1002/9780470132395.ch6.
Brett L. Lucht; David B. Collum. Ethereal Solvation of Lithium Hexamethyldisilazide: Unexpected Relationships of Solvation Number, Solvation Energy, and Aggregation State. Journal of the American Chemical Society. 1995, s. 9863–9874. doi:10.1021/ja00144a012.
Brett L. Lucht; David B. Collum. Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide (LiHMDS). Journal of the American Chemical Society. 1996, s. 2217–2225. doi:10.1021/ja953029p.
R. Neufeld; R. Collum; R. Herbst-Irmer; R. Schöne; E. Stalke. Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M = Li, Na, K, Rb and Cs) with Ammonia. Chemistry—A European Journal. 2016, s. 12340–12346. doi:10.1002/chem.201600833. PMID 27457218.
Robin D. Rogers; Jerry L. Atwood; Rainer Grüning. The crystal structure of N-lithiohexamethyldisilazane, [LiN(SiMe₃)₂]₃. Journal of Organometallic Chemistry. 1978, s. 229–237. doi:10.1016/S0022-328X(00)92291-5.
George Wu; Mingsheng Huang. Organolithium Reagents in Pharmaceutical Asymmetric Processes. Chemical Reviews. 2006, s. 2596–2616. doi:10.1021/cr040694k. PMID 16836294.
Robert R. Fraser; Tarek S. Mansour; Sylvain Savard. Acidity measurements on pyridines in tetrahydrofuran using lithiated silylamines. The Journal of Organic Chemistry. 1985, s. 3232–3234. doi:10.1021/jo00217a050.
A. Maaninen; J. Shvari; R. S. Laitinen; T. Chivers. Compounds of General Interest. Inorganic Syntheses. 2002, s. 196–199. doi:10.1002/0471224502.ch4.
Michael Lappert; Andrey Protchenko; Philip Power; Alexandra Seeber. Metal Amide Chemistry. Weinheim: Wiley-VCH, 2009. Dostupné online. doi:10.1002/9780470740385. S. 196–199.

nih.gov

ncbi.nlm.nih.gov

R. Neufeld; R. Collum; R. Herbst-Irmer; R. Schöne; E. Stalke. Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M = Li, Na, K, Rb and Cs) with Ammonia. Chemistry—A European Journal. 2016, s. 12340–12346. doi:10.1002/chem.201600833. PMID 27457218.
George Wu; Mingsheng Huang. Organolithium Reagents in Pharmaceutical Asymmetric Processes. Chemical Reviews. 2006, s. 2596–2616. doi:10.1021/cr040694k. PMID 16836294.

pubchem.ncbi.nlm.nih.gov

Lithium bis(trimethylsilyl)amide. pubchem.ncbi.nlm.nih.gov [online]. PubChem [cit. 2021-05-24]. Dostupné online. (anglicky)

orgsyn.org

DANHEISER, R. L.; MILLER, R. F.; BRISBOIS, R. G. Detrifluoroacetylative Diazo Group Transfer: (E)-1-Diazo-4-phenyl-3-buten-2-one. Org. Synth.. 1990, s. 134. Dostupné online. ; Coll. Vol.. S. 197.

uni-goettingen.de

ediss.uni-goettingen.de

Neufeld, R.: DOSY External Calibration Curve Molecular Weight Determination as a Valuable Methodology in Characterizing Reactive Intermediates in Solution. In: eDiss, Georg-August-Universität Göttingen. 2016.