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Lithium bis(trimethylsilyl)amide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lithium bis(trimethylsilyl)amide" in English language version.

refsWebsite
Global rank English rank
10doi.org
2nd place
2nd place
2nih.gov
4th place
4th place
2harvard.edu
18th place
17th place
1orgsyn.org
2,971st place
2,826th place
1uni-goettingen.de
2,594th place
2,546th place

doi.org

  • Amonoo-Neizer, E. H.; Shaw, R. A.; Skovlin, D. O.; Smith, B. C. (1966). "Lithium Bis(trimethylsilyl)amide and Tris(trimethylsilyl)amine". Inorganic Syntheses. Vol. 8. pp. 19–22. doi:10.1002/9780470132395.ch6. ISBN 978-0-470-13239-5. {{cite book}}: |journal= ignored (help)
  • Wu, George; Huang, Mingsheng (July 2006). "Organolithium Reagents in Pharmaceutical Asymmetric Processes". Chemical Reviews. 106 (7): 2596–2616. doi:10.1021/cr040694k. PMID 16836294.
  • Fraser, Robert R.; Mansour, Tarek S.; Savard, Sylvain (August 1985). "Acidity measurements on pyridines in tetrahydrofuran using lithiated silylamines". The Journal of Organic Chemistry. 50 (17): 3232–3234. doi:10.1021/jo00217a050.
  • Maaninen, A.; Shvari, J.; Laitinen, R. S.; Chivers, T (2002). "Compounds of General Interest". In Coucouvanis, Dimitri (ed.). Inorganic Syntheses. Vol. 33. New York: John Wiley & Sons, Inc. pp. 196–199. doi:10.1002/0471224502.ch4. ISBN 9780471208259.
  • Michael Lappert, Andrey Protchenko, Philip Power, Alexandra Seeber (2009). Metal Amide Chemistry. Weinheim: Wiley-VCH. doi:10.1002/9780470740385. ISBN 978-0-470-72184-1.{{cite book}}: CS1 maint: multiple names: authors list (link)
  • Hämäläinen, Jani; Holopainen, Jani; Munnik, Frans; Hatanpää, Timo; Heikkilä, Mikko; Ritala, Mikko; Leskelä, Markku (2012). "Lithium Phosphate Thin Films Grown by Atomic Layer Deposition". Journal of the Electrochemical Society. 159 (3): A259 – A263. doi:10.1149/2.052203jes.
  • Lucht, Brett L.; Collum, David B. (1995). "Ethereal Solvation of Lithium Hexamethyldisilazide: Unexpected Relationships of Solvation Number, Solvation Energy, and Aggregation State". Journal of the American Chemical Society. 117 (39): 9863–9874. Bibcode:1995JAChS.117.9863L. doi:10.1021/ja00144a012.
  • Lucht, Brett L.; Collum, David B. (1996). "Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide (LiHMDS)". Journal of the American Chemical Society. 118 (9): 2217–2225. Bibcode:1996JAChS.118.2217L. doi:10.1021/ja953029p.
  • Neufeld, R.; Michel, R.; Herbst-Irmer, R.; Schöne, R.; Stalke, D. (2016). "Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M = Li, Na, K, Rb and Cs) with Ammonia". Chem. Eur. J. 22 (35): 12340–12346. doi:10.1002/chem.201600833. PMID 27457218.
  • Rogers, Robin D.; Atwood, Jerry L.; Grüning, Rainer (1978). "The crystal structure of N-lithiohexamethyldisilazane, [LiN(SiMe3)2]3". J. Organomet. Chem. 157 (2): 229–237. doi:10.1016/S0022-328X(00)92291-5.

harvard.edu

ui.adsabs.harvard.edu

  • Lucht, Brett L.; Collum, David B. (1995). "Ethereal Solvation of Lithium Hexamethyldisilazide: Unexpected Relationships of Solvation Number, Solvation Energy, and Aggregation State". Journal of the American Chemical Society. 117 (39): 9863–9874. Bibcode:1995JAChS.117.9863L. doi:10.1021/ja00144a012.
  • Lucht, Brett L.; Collum, David B. (1996). "Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide (LiHMDS)". Journal of the American Chemical Society. 118 (9): 2217–2225. Bibcode:1996JAChS.118.2217L. doi:10.1021/ja953029p.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wu, George; Huang, Mingsheng (July 2006). "Organolithium Reagents in Pharmaceutical Asymmetric Processes". Chemical Reviews. 106 (7): 2596–2616. doi:10.1021/cr040694k. PMID 16836294.
  • Neufeld, R.; Michel, R.; Herbst-Irmer, R.; Schöne, R.; Stalke, D. (2016). "Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M = Li, Na, K, Rb and Cs) with Ammonia". Chem. Eur. J. 22 (35): 12340–12346. doi:10.1002/chem.201600833. PMID 27457218.

orgsyn.org

uni-goettingen.de

ediss.uni-goettingen.de