Organolithné sloučeniny (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organolithné sloučeniny" in Czech language version.

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acs.org

pubs.acs.org

  • POWER, P.P; HOPE H. Isolation and crystal structures of the halide-free and halide-rich phenyllithium etherate complexes [(PhLi.Et2O)4] and [(PhLi.Et2O)3.LiBr].. JACS. 1983, s. 5320–5324. Dostupné online. doi:10.1021/ja00354a022. 
  • REICH, H.J; GREEN, D.P. Spectroscopic and Reactivity Studies of Lithium Reagent - HMPA Complexes. JACS. 1989, s. 8729–8731. Dostupné online. doi:10.1021/ja00205a030. 
  • WILLIARD, P.G; NICHOLS, M.A. Solid-state structures of n-butyllithium-TMEDA, -THF, and -DME complexes. JACS. 1993, s. 1568–1572. Dostupné online. doi:10.1021/ja00057a050. 
  • ASHBY, E.C.; NODING, S.R. The effects of added salts on the stereoselectivity and rate of organometallic compound addition to ketones. J. Org. Chem.. 1979, s. 4371–4377. Dostupné online. doi:10.1021/jo01338a026. 
  • COHEN, T; BHUPATHY. M. Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers. Acc. Chem. Res.. 1989, s. 152–161. Dostupné online. doi:10.1021/ar00160a006. 
  • SNIECKUS, V. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics. Chem. Rev.. 1990, s. 879–933. Dostupné online. doi:10.1021/cr00104a001. 
  • KOFRON, W.G.; BACLAWSKI, L.M. A convenient method for estimation of alkyllithium concentrations. J. Org. Chem.. 1976, s. 1879–1880. Dostupné online. doi:10.1021/jo00872a047. 

doi.org

  • ZABICKY, Jacob. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0304. Kapitola Analytical aspects of organolithium compounds. 
  • EISCH, John J. Henry Gilman: American Pioneer in the Rise of Organometallic Chemistry in Modern Science and Technology†. Organometallics. 2002, s. 5439–5463. ISSN 0276-7333. doi:10.1021/om0109408. 
  • STEY, Thomas; STALKE, Dietmar. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0298. Kapitola Lead structures in lithium organic chemistry. 
  • REICH, Hans J. Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms. Chemical Reviews. 2013, s. 7130–7178. doi:10.1021/cr400187u. PMID 23941648. 
  • STROHMANN, C. Structure Formation Principles and Reactivity of Organolithium Compounds.. Chem. Eur. J.. 2009, s. 3320–3334. Dostupné online. doi:10.1002/chem.200900041. 
  • JEMMIS, E.D.; GOPAKUMAR, G. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0297. Kapitola Theoretical studies in organolithium chemistry. 
  • Streiwieser, A. Perspectives on Computational Organic Chemistry. J. Org. Chem.. 2009, s. 4433–4446. doi:10.1021/jo900497s. 
  • Bickelhaupt, F. M. Covalency in Highly Polar Bonds. Structure and Bonding of Methylalkalimetal Oligomers (CH3M)n (M = Li−Rb; n = 1, 4). J. Chem. Theory Comput.. 2006, s. 965–980. doi:10.1021/ct050333s. 
  • POWER, P.P; HOPE H. Isolation and crystal structures of the halide-free and halide-rich phenyllithium etherate complexes [(PhLi.Et2O)4] and [(PhLi.Et2O)3.LiBr].. JACS. 1983, s. 5320–5324. Dostupné online. doi:10.1021/ja00354a022. 
  • Williard, P. G.; SALVINO, J. M. Synthesis, isolation, and structure of an LDA-THF complex. Journal of Organic Chemistry. 1993, s. 1–3. doi:10.1021/jo00053a001. 
  • HILMERSSON, Goran; GRANANDER, Johan. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0342. Kapitola Structure and dynamics of chiral lithium amides. 
  • Collum, D.B. Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis. Angew. Chem. Int. Ed.. 2007, s. 3002–3017. doi:10.1002/anie.200603038. 
  • Sekiguchi, Akira. Lithiosilanes and their application to the synthesis of polysilane dendrimers. Coord. Chem. Rev.. 2000, s. 11–45. doi:10.1016/S0010-8545(00)00315-5. 
  • Collum, D. B. Solution Structures of Lithium Enolates, Phenolates, Carboxylates, and Alkoxides in the Presence of N,N,N′,N′-Tetramethylethylenediamine: A Prevalence of Cyclic Dimers. J. Org. Chem.. 2008, s. 7743–7747. doi:10.1021/jo801532d. 
  • Reich, H. J. Aggregation and reactivity of phenyllithium solutions. J. Am. Chem. Soc.. 1998, s. 7201–7210. doi:10.1021/ja980684z. 
  • McGarrity, J. F.; OGLE, C.A. High-field proton NMR study of the aggregation and complexation of n-butyllithium in tetrahydrofuran. J. Am. Chem. Soc.. 1985, s. 1805–1810. doi:10.1021/ja00293a001. 
  • Reich, H. J. What's going on with these lithium reagents. J. Org. Chem.. 2012, s. 5471–5491. doi:10.1021/jo3005155. 
  • Strohmann, C.,; GESSNER, V.H. Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene. J. Am. Chem. Soc.. 2008, s. 11719–11725. doi:10.1021/ja8017187. PMID 18686951. 
  • Collum, D. B. Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis. Angew. Chem. Int. Ed.. 2007, s. 3002–3017. doi:10.1002/anie.200603038. 
  • CHALK, A.J; HOOGEBOOM, T.J. Ring metalation of toluene by butyllithium in the presence of N,N,N′,N′-tetramethylethylenediamine. J. Organomet. Chem. 1968, s. 615–618. Dostupné online. doi:10.1016/0022-328x(68)80091-9. 
  • REICH, H.J; GREEN, D.P. Spectroscopic and Reactivity Studies of Lithium Reagent - HMPA Complexes. JACS. 1989, s. 8729–8731. Dostupné online. doi:10.1021/ja00205a030. 
  • WILLIARD, P.G; NICHOLS, M.A. Solid-state structures of n-butyllithium-TMEDA, -THF, and -DME complexes. JACS. 1993, s. 1568–1572. Dostupné online. doi:10.1021/ja00057a050. 
  • Collum, D.B. Is N,N,N,N-Tetramethylethylenediamine a Good Ligand for Lithium?. Acc. Chem. Res.. 1992, s. 448–454. doi:10.1021/ar00022a003. 
  • Bernstein, M.P.; COLLUM, D.B. Solvent- and substrate-dependent rates of imine metalations by lithium diisopropylamide: understanding the mechanisms underlying krel. J. Am. Chem. Soc.. 1993, s. 8008–8010. doi:10.1021/ja00071a011. 
  • SEEBACH, D. Structure and Reactivity of Lithium Enolates. From Pinacolone to Selective C-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures.. Angew. Chem. Int. Ed.. 1988, s. 1624–1654. Dostupné online. doi:10.1002/anie.198816241. 
  • FANANAS, Francisco; SANZ, Roberto. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0341. Kapitola Intramolecular carbolithiation reactions. 
  • Heinz-Dieter Brandt, Wolfgang Nentwig1, Nicola Rooney, Ronald T. LaFlair, Ute U. Wolf, John Duffy, Judit E. Puskas, Gabor Kaszas, Mark Drewitt, Stephan Glander "Rubber, 5. Solution Rubbers" in Ullmann's Encyclopedia of Industrial Chemistry, 2011, Wiley-VCH, Weinheim. doi:10.1002/14356007.o23_o02
  • BASKARA, D.; MULLER, A.H. Controlled and living polymerizations: From mechanisms to applications. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA,, 2010. ISBN 9783527629091. doi:10.1002/9783527629091.ch1. Kapitola Anionic Vinyl Polymerization. 
  • Bailey, W.F. Preparation and facile cyclization of 5-alkyn-1-yllithiums. Tetrahedron Lett.. 1989, s. 3901–3904. doi:10.1016/S0040-4039(00)99279-7. 
  • ASHBY, E.C.; NODING, S.R. The effects of added salts on the stereoselectivity and rate of organometallic compound addition to ketones. J. Org. Chem.. 1979, s. 4371–4377. Dostupné online. doi:10.1021/jo01338a026. 
  • YAMATAKA, Hiroshi. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0310. Kapitola Addition of organolithium reagents to double bonds. 
  • Landa, S. Über adamantan und dessen derivate IX. In 2-stellung substituierte derivate. Czech. Chem. Commun.. 1967, s. 570–575. doi:10.1135/cccc19670570. 
  • Rubottom, G.M.; KIM, C. Preparation of methyl ketones by the sequential treatment of carboxylic acids with methyllithium and chlorotrimethylsilane. J. Org. Chem.. 1983, s. 1550–1552. doi:10.1021/jo00157a038. 
  • Zadel, G.; BREITMAIER, E. A One-Pot Synthesis of Ketones and Aldehydes from Carbon Dioxide and Organolithium Compounds. Angew. Chem. Int. Ed.. 1992, s. 1035–1036. doi:10.1002/anie.199210351. 
  • Ronald, R.C. Methoxymethyl ethers. An activating group for rapid and regioselective metalation. Tetrahedron Lett.. 1975, s. 3973–3974. doi:10.1016/S0040-4039(00)91212-7. 
  • Hunt, D.A. Michael addition of organolithium compounds. A Review,. Org. Prep. Proc. Int.. 1989, s. 705–749. doi:10.1080/00304948909356219. 
  • Reich, H. J.; SIKORSKI, W. H. Regioselectivity of Addition of Organolithium Reagents to Enones: The Role of HMPA. J. Org. Chem.. 1999, s. 14–15. doi:10.1021/jo981765g. 
  • Collum, D.B. NMR Spectroscopic Investigations of Mixed Aggregates Underlying Highly Enantioselective 1,2-Additions of Lithium Cyclopropylacetylide to Quinazolinones. J. Am. Chem. Soc.. 2001, s. 9135–9143. doi:10.1021/ja0105616. 
  • Sommmer, L.H.; KORTE, W. D. Stereospecific coupling reactions between organolithium reagents and secondary halides. J. Org. Chem.. 1970, s. 22–25. doi:10.1021/jo00826a006. 
  • HOPPE, Dieter; CHRISTOPH, Guido. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0313. Kapitola Asymmetric deprotonation with alkyllithium– (−)-sparteine. 
  • CLAYDEN, Jonathan. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0306. Kapitola Directed metallization of aromatic compounds. 
  • SCHLOSSER, M. Superbases for organic synthesis. Pure Appl. Chem.. 1988, s. 1627–1634. doi:10.1351/pac198860111627. 
  • Roush, W.R. Enantioselective synthesis using diisopropyl tartrate modified (E)- and (Z)-crotylboronates: Reactions with achiral aldehydes. Tetrahedron Lett.. 1988, s. 5579–5582. doi:10.1016/S0040-4039(00)80816-3. 
  • Park, Y.S. (−)-Sparteine-Mediated α-Lithiation of N-Boc-N-(p-methoxyphenyl)benzylamine: Enantioselective Syntheses of (S) and (R) Mono- and Disubstituted N-Boc-benzylamines. J. Am. Chem. Soc.. 1996, s. 3757–3758. doi:10.1021/ja9538804. 
  • VALNOT, Jean-Yves; MADDALUNO, Jacques. PATAI'S Chemistry of Functional Groups.. [s.l.]: John Wiley & Sons, Ltd, 2009. ISBN 9780470682531. doi:10.1002/9780470682531.pat0345. Kapitola Aspects of the synthesis, structure and reactivity of lithium enolates. 
  • Ireland. R. E. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation. J. Am. Chem. Soc.. 1976, s. 2868–2877. doi:10.1021/ja00426a033. 
  • GILMAN, Henry; LANGHAM, Wright; JACOBY, Arthur L. Metalation as a Side Reaction in the Preparation of Organolithium Compounds. Journal of the American Chemical Society. 1939, s. 106–109. ISSN 0002-7863. doi:10.1021/ja01870a036. 
  • Bailey, W. F.; PATRICIA, J. F. The mechanism of the lithium - halogen Interchange reaction : a review of the literature. J. Organomet. Chem.. 1988, s. 1–46. doi:10.1016/0022-328X(88)83017-1. 
  • ; CALABRESE, J. C. Novel hypervalent (10-I-2) iodine structures author = Farnham, W. B.. J. Am. Chem. Soc.. 1986, s. 2449–2451. doi:10.1021/ja00269a055. 
  • Rogers, H. R.; HOUK, J. Preliminary studies of the mechanism of metal-halogen exchange. The kinetics of reaction of n-butyllithium with substituted bromobenzenes in hexane solution. J. Am. Chem. Soc.. 1982, s. 522–525. doi:10.1021/ja00366a024. 
  • Fischer, H. Electron spin resonance of transient alkyl radicals during alkyllithium-alkyl halide reactions. J. Phys. Chem.. 1969, s. 3834–3838. doi:10.1021/j100845a044. 
  • BAILEY, W.F. Metal—halogen interchange between t-butyllithium and 1-iodo-5-hexenes provides no evidence for single-electron transfer. Tetrahedron Lett.. 1986, s. 1861–1864. Dostupné online. doi:10.1016/s0040-4039(00)84395-6. 
  • SEEBACH, D; NEUMANN H. Stereospecific preparation of terminal vinyllithium derivatives by Br/Li-exchange with t-butyllithium. Tetrahedron Lett.. 1976, s. 4839–4842. Dostupné online. doi:10.1016/s0040-4039(00)78926-x. 
  • Toth, J. E.; HAMANN, P.R.; FUCHS, P.L. Studies culminating in the total synthesis of (dl)-morphine. J. Org. Chem.. 1988, s. 4694–4708. doi:10.1021/jo00255a008. 
  • Parham, W.P.; BRADSHER, C.K. Aromatic organolithium reagents bearing electrophilic groups. Preparation by halogen-lithium exchange. Acc. Chem. Res.. 1982, s. 300–305. doi:10.1021/ar00082a001. 
  • Sotomayor, N.; LETE, E. Aryl and Heteroaryllithium Compounds by Metal - Halogen Exchange. Synthesis of Carbocyclic and Heterocyclic Systems. Curr. Org. Chem.. 2003, s. 275–300. doi:10.2174/1385272033372987. 
  • Quin, C. Synthesis of a mitochondria-targeted spin trap using a novel Parham-type cyclization. Tetrahedron. 2009, s. 8154–8160. doi:10.1016/j.tet.2009.07.081. 
  • Corey, E.J.; WOLLENBERG, R.H. Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation. J. Org. Chem.. 1975, s. 2265–2266. doi:10.1021/jo00903a037. 
  • Reeder, M.R. An Improved Method for the Palladium Cross-Coupling Reaction of Oxazol-2-ylzinc Derivatives with Aryl Bromides. Org. Process Res. Dev.. 2003, s. 696–699. doi:10.1021/op034059c. 
  • Nakamura, E. Reaction Pathway of the Conjugate Addition of Lithium Organocuprate Clusters to Acrolein. J. Am. Chem. Soc.. 1997, s. 4900–4910. doi:10.1021/ja964209h. 
  • Si-Fodil, M. Obtention of 2,2-(diethoxy) vinyl lithium and 2-methyl-4-ethoxy butadienyl lithium by arene-catalysed lithiation of the corresponding chloro derivatives. Synthetic applications. Tetrahedron Lett.. 1998, s. 8975–8978. doi:10.1016/S0040-4039(98)02031-0. 
  • COHEN, T; BHUPATHY. M. Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers. Acc. Chem. Res.. 1989, s. 152–161. Dostupné online. doi:10.1021/ar00160a006. 
  • SNIECKUS, V. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics. Chem. Rev.. 1990, s. 879–933. Dostupné online. doi:10.1021/cr00104a001. 
  • SCHWINDEMAN, James A.; WOLTERMANN, Chris J.; LETCHFORD, Robert J. Safe handling of organolithium compounds in the laboratory. Chemical Health and Safety. 2002, s. 6–11. ISSN 1074-9098. doi:10.1016/S1074-9098(02)00295-2. 
  • GELLERT, H; ZIEGLER, K. Organoalkali compounds. XVI. The thermal stability of lithium alkyls.. Liebigs Ann. Chem.. 1950, s. 179–185. doi:10.1002/jlac.19505670110. 
  • KOFRON, W.G.; BACLAWSKI, L.M. A convenient method for estimation of alkyllithium concentrations. J. Org. Chem.. 1976, s. 1879–1880. Dostupné online. doi:10.1021/jo00872a047. 
  • Stanetty, P.; KOLLER, H.; MIHOVILOVIC, M. Directed Ortho-Lithiation of Phenylcarbamic Acid 1,l-Dimethylethyl Ester (N-Boc-aniline). Revision and Improvements. J. Org. Chem.. 1992, s. 6833–6837. doi:10.1021/jo00051a030. 

els-cdn.com

ac.els-cdn.com

  • CHALK, A.J; HOOGEBOOM, T.J. Ring metalation of toluene by butyllithium in the presence of N,N,N′,N′-tetramethylethylenediamine. J. Organomet. Chem. 1968, s. 615–618. Dostupné online. doi:10.1016/0022-328x(68)80091-9. 
  • BAILEY, W.F. Metal—halogen interchange between t-butyllithium and 1-iodo-5-hexenes provides no evidence for single-electron transfer. Tetrahedron Lett.. 1986, s. 1861–1864. Dostupné online. doi:10.1016/s0040-4039(00)84395-6. 
  • SEEBACH, D; NEUMANN H. Stereospecific preparation of terminal vinyllithium derivatives by Br/Li-exchange with t-butyllithium. Tetrahedron Lett.. 1976, s. 4839–4842. Dostupné online. doi:10.1016/s0040-4039(00)78926-x. 

nih.gov

ncbi.nlm.nih.gov

  • REICH, Hans J. Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms. Chemical Reviews. 2013, s. 7130–7178. doi:10.1021/cr400187u. PMID 23941648. 
  • Strohmann, C.,; GESSNER, V.H. Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene. J. Am. Chem. Soc.. 2008, s. 11719–11725. doi:10.1021/ja8017187. PMID 18686951. 

wiley.com

onlinelibrary.wiley.com

  • STROHMANN, C. Structure Formation Principles and Reactivity of Organolithium Compounds.. Chem. Eur. J.. 2009, s. 3320–3334. Dostupné online. doi:10.1002/chem.200900041. 
  • SEEBACH, D. Structure and Reactivity of Lithium Enolates. From Pinacolone to Selective C-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures.. Angew. Chem. Int. Ed.. 1988, s. 1624–1654. Dostupné online. doi:10.1002/anie.198816241. 

wisc.edu

chem.wisc.edu

worldcat.org

  • EISCH, John J. Henry Gilman: American Pioneer in the Rise of Organometallic Chemistry in Modern Science and Technology†. Organometallics. 2002, s. 5439–5463. ISSN 0276-7333. doi:10.1021/om0109408. 
  • GILMAN, Henry; LANGHAM, Wright; JACOBY, Arthur L. Metalation as a Side Reaction in the Preparation of Organolithium Compounds. Journal of the American Chemical Society. 1939, s. 106–109. ISSN 0002-7863. doi:10.1021/ja01870a036. 
  • SCHWINDEMAN, James A.; WOLTERMANN, Chris J.; LETCHFORD, Robert J. Safe handling of organolithium compounds in the laboratory. Chemical Health and Safety. 2002, s. 6–11. ISSN 1074-9098. doi:10.1016/S1074-9098(02)00295-2.