Sign In

Login

Password

Forgot Password ? Sign Up

Organolithium reagent (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organolithium reagent" in English language version.

refsWebsite
Global rank English rank
61doi.org
2nd place
2nd place
14nih.gov
4th place
4th place
3worldcat.org
5th place
5th place
2wiley.com
222nd place
297th place
1organicchemistrydata.org
low place
low place
1scripps.edu
low place
low place
1tamu.edu
1,672nd place
1,262nd place

doi.org

  • Zabicky, Jacob (2009). "Analytical aspects of organolithium compounds". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0304. ISBN 9780470682531.
  • Wu, G.; Huang, M. (2006). "Organolithium Reagents in Pharmaceutical Asymmetric Processes". Chem. Rev. 106 (7): 2596–2616. doi:10.1021/cr040694k. PMID 16836294.
  • Eisch, John J. (2002). "Henry Gilman: American Pioneer in the Rise of Organometallic Chemistry in Modern Science and Technology†". Organometallics. 21 (25): 5439–5463. doi:10.1021/om0109408. ISSN 0276-7333.
  • Stey, Thomas; Stalke, Dietmar (2009). "Lead structures in lithium organic chemistry". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0298. ISBN 9780470682531.
  • Reich, Hans J. (2013). "Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms". Chemical Reviews. 113 (9): 7130–7178. doi:10.1021/cr400187u. PMID 23941648.
  • Strohmann, C; et al. (2009). "Structure Formation Principles and Reactivity of Organolithium Compounds" (PDF). Chem. Eur. J. 15 (14): 3320–3334. doi:10.1002/chem.200900041. PMID 19260001.
  • Jemmis, E.D.; Gopakumar, G. (2009). "Theoretical studies in organolithium chemistry". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0297. ISBN 9780470682531.
  • Streiwieser, A. (2009). "Perspectives on Computational Organic Chemistry". J. Org. Chem. 74 (12): 4433–4446. doi:10.1021/jo900497s. PMC 2728082. PMID 19518150.
  • Bickelhaupt, F. M.; et al. (2006). "Covalency in Highly Polar Bonds. Structure and Bonding of Methylalkalimetal Oligomers (CH3M)n (M = Li−Rb; n = 1, 4)". J. Chem. Theory Comput. 2 (4): 965–980. doi:10.1021/ct050333s. PMID 26633056.
  • Weiss, Erwin (November 1993). "Structures of Organo Alkali Metal Complexes and Related Compounds". Angewandte Chemie International Edition in English. 32 (11): 1501–1523. doi:10.1002/anie.199315013. ISSN 0570-0833.
  • Fraenkel, G.; Qiu, Fayang (1996). "Observation of a Partially Delocalized Allylic Lithium and the Dynamics of Its 1,3 Lithium Sigmatropic Shift". J. Am. Chem. Soc. 118 (24): 5828–5829. doi:10.1021/ja960440j.
  • Fraenkel. G; et al. (1995). "The carbon-lithium bond in monomeric arllithium: Dynamics of exchange, relaxation and rotation". J. Am. Chem. Soc. 117 (23): 6300–6307. doi:10.1021/ja00128a020.
  • Power, P.P; Hope H. (1983). "Isolation and crystal structures of the halide-free and halide-rich phenyllithium etherate complexes [(PhLi.Et2O)4] and [(PhLi.Et2O)3.LiBr]". Journal of the American Chemical Society. 105 (16): 5320–5324. doi:10.1021/ja00354a022.
  • Williard, P. G.; Salvino, J. M. (1993). "Synthesis, isolation, and structure of an LDA-THF complex". Journal of Organic Chemistry. 58 (1): 1–3. doi:10.1021/jo00053a001.
  • Hilmersson, Goran; Granander, Johan (2009). "Structure and dynamics of chiral lithium amides". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0342. ISBN 9780470682531.
  • Collum, D.B.; et al. (2007). "Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis". Angew. Chem. Int. Ed. 49 (17): 3002–3017. doi:10.1002/anie.200603038. PMID 17387670.
  • Sekiguchi, Akira.; et al. (2000). "Lithiosilanes and their application to the synthesis of polysilane dendrimers". Coord. Chem. Rev. 210: 11–45. doi:10.1016/S0010-8545(00)00315-5.
  • Collum, D. B.; et al. (2008). "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. 73 (19): 7743–7747. doi:10.1021/jo801532d. PMC 2636848. PMID 18781812.
  • Reich, H. J.; et al. (1998). "Aggregation and reactivity of phenyllithium solutions". J. Am. Chem. Soc. 120 (29): 7201–7210. doi:10.1021/ja980684z.
  • McGarrity, J. F.; Ogle, C.A. (1985). "High-field proton NMR study of the aggregation and complexation of n-butyllithium in tetrahydrofuran". J. Am. Chem. Soc. 107 (7): 1805–1810. doi:10.1021/ja00293a001.
  • Reich, H. J. (2012). "What's going on with these lithium reagents". J. Org. Chem. 77 (13): 5471–5491. doi:10.1021/jo3005155. PMID 22594379.
  • Strohmann, C.; Gessner, V.H. (2008). "Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene". J. Am. Chem. Soc. 130 (35): 11719–11725. doi:10.1021/ja8017187. PMID 18686951.
  • Collum, D. B.; et al. (2007). "Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis". Angew. Chem. Int. Ed. 46 (17): 3002–3017. doi:10.1002/anie.200603038. PMID 17387670.
  • Chalk, A.J; Hoogeboom, T.J (1968). "Ring metalation of toluene by butyllithium in the presence of N,N,N′,N′-tetramethylethylenediamine". J. Organomet. Chem. 11: 615–618. doi:10.1016/0022-328x(68)80091-9.
  • Reich, H.J; Green, D.P (1989). "Spectroscopic and Reactivity Studies of Lithium Reagent - HMPA Complexes". Journal of the American Chemical Society. 111 (23): 8729–8731. doi:10.1021/ja00205a030.
  • Williard, P.G; Nichols, M.A (1993). "Solid-state structures of n-butyllithium-TMEDA, -THF, and -DME complexes". Journal of the American Chemical Society. 115 (4): 1568–1572. doi:10.1021/ja00057a050.
  • Collum, D.B. (1992). "Is N,N,N,N-Tetramethylethylenediamine a Good Ligand for Lithium?". Acc. Chem. Res. 25 (10): 448–454. doi:10.1021/ar00022a003.
  • Bernstein, M.P.; Collum, D.B. (1993). "Solvent- and substrate-dependent rates of imine metalations by lithium diisopropylamide: understanding the mechanisms underlying krel". J. Am. Chem. Soc. 115 (18): 8008–8010. doi:10.1021/ja00071a011.
  • Seebach, D (1988). "Structure and Reactivity of Lithium Enolates. From Pinacolone to Selective C-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures" (PDF). Angew. Chem. Int. Ed. 27 (12): 1624–1654. doi:10.1002/anie.198816241.
  • Fananas, Francisco; Sanz, Roberto (2009). "Intramolecular carbolithiation reactions". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0341. ISBN 9780470682531.
  • 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
  • Baskaran, D.; Müller, A.H. (2010). "Anionic Vinyl Polymerization". Controlled and living polymerizations: From mechanisms to applications. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA. doi:10.1002/9783527629091.ch1. ISBN 9783527629091.
  • Bailey, W.F.; et al. (1989). "Preparation and facile cyclization of 5-alkyn-1-yllithiums". Tetrahedron Lett. 30 (30): 3901–3904. doi:10.1016/S0040-4039(00)99279-7.
  • Ashby, E.C.; Noding, S.R. (1979). "The effects of added salts on the stereoselectivity and rate of organometallic compound addition to ketones". J. Org. Chem. 44 (24): 4371–4377. doi:10.1021/jo01338a026.
  • Yamataka, Hiroshi (2009). "Addition of organolithium reagents to double bonds". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0310. ISBN 9780470682531.
  • Landa, S.; et al. (1967). "Über adamantan und dessen derivate IX. In 2-stellung substituierte derivate". Collection of Czechoslovak Chemical Communications. 72 (2): 570–575. doi:10.1135/cccc19670570.
  • Rubottom, G.M.; Kim, C (1983). "Preparation of methyl ketones by the sequential treatment of carboxylic acids with methyllithium and chlorotrimethylsilane". J. Org. Chem. 48 (9): 1550–1552. doi:10.1021/jo00157a038.
  • Zadel, G.; Breitmaier, E. (1992). "A One-Pot Synthesis of Ketones and Aldehydes from Carbon Dioxide and Organolithium Compounds". Angew. Chem. Int. Ed. 31 (8): 1035–1036. doi:10.1002/anie.199210351.
  • Ronald, R.C. (1975). "Methoxymethyl ethers. An activating group for rapid and regioselective metalation". Tetrahedron Lett. 16 (46): 3973–3974. doi:10.1016/S0040-4039(00)91212-7.
  • Hunt, D.A. (1989). "Michael addition of organolithium compounds. A Review". Org. Prep. Proc. Int. 21 (6): 705–749. doi:10.1080/00304948909356219.
  • Reich, H. J.; Sikorski, W. H. (1999). "Regioselectivity of Addition of Organolithium Reagents to Enones: The Role of HMPA". J. Org. Chem. 64 (1): 14–15. doi:10.1021/jo981765g. PMID 11674078.
  • Collum, D.B.; et al. (2001). "NMR Spectroscopic Investigations of Mixed Aggregates Underlying Highly Enantioselective 1,2-Additions of Lithium Cyclopropylacetylide to Quinazolinones". J. Am. Chem. Soc. 123 (37): 9135–9143. doi:10.1021/ja0105616. PMID 11552822.
  • Sommmer, L.H.; Korte, W. D. (1970). "Stereospecific coupling reactions between organolithium reagents and secondary halides". J. Org. Chem. 35: 22–25. doi:10.1021/jo00826a006.
  • Hoppe, Dieter; Christoph, Guido (2009). "Asymmetric deprotonation with alkyllithium– (−)-sparteine". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0313. ISBN 9780470682531.
  • Clayden, Jonathan (2009). "Directed metallization of aromatic compounds". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0306. ISBN 9780470682531.
  • Schlosser, M (1988). "Superbases for organic synthesis". Pure Appl. Chem. 60 (11): 1627–1634. doi:10.1351/pac198860111627.
  • Roush, W.R.; et al. (1988). "Enantioselective synthesis using diisopropyl tartrate modified (E)- and (Z)-crotylboronates: Reactions with achiral aldehydes". Tetrahedron Lett. 29 (44): 5579–5582. doi:10.1016/S0040-4039(00)80816-3.
  • Park, Y.S.; et al. (1996). "(−)-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. 118 (15): 3757–3758. doi:10.1021/ja9538804.
  • Valnot, Jean-Yves; Maddaluno, Jacques (2009). "Aspects of the synthesis, structure and reactivity of lithium enolates". PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd. doi:10.1002/9780470682531.pat0345. ISBN 9780470682531.
  • Ireland. R. E.; et al. (1976). "The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation". J. Am. Chem. Soc. 98 (10): 2868–2877. doi:10.1021/ja00426a033.
  • Parham, W.P.; Bradsher, C.K. (1982). "Aromatic organolithium reagents bearing electrophilic groups. Preparation by halogen-lithium exchange". Acc. Chem. Res. 15 (10): 300–305. doi:10.1021/ar00082a001.
  • Corey, E.J.; Wollenberg, R.H. (1975). "Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation". J. Org. Chem. 40 (15): 2265–2266. doi:10.1021/jo00903a037.
  • Reeder, M.R.; et al. (2003). "An Improved Method for the Palladium Cross-Coupling Reaction of Oxazol-2-ylzinc Derivatives with Aryl Bromides". Org. Process Res. Dev. 7 (5): 696–699. doi:10.1021/op034059c.
  • Nakamura, E.; et al. (1997). "Reaction Pathway of the Conjugate Addition of Lithium Organocuprate Clusters to Acrolein". J. Am. Chem. Soc. 119 (21): 4900–4910. doi:10.1021/ja964209h.
  • Si-Fodil, M.; et al. (1998). "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. 39 (49): 8975–8978. doi:10.1016/S0040-4039(98)02031-0.
  • Cohen, T; Bhupathy. M (1989). "Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers". Acc. Chem. Res. 22 (4): 152–161. doi:10.1021/ar00160a006.
  • Snieckus, V (1990). "Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics". Chem. Rev. 90 (6): 879–933. doi:10.1021/cr00104a001.
  • Schwindeman, James A.; Woltermann, Chris J.; Letchford, Robert J. (2002). "Safe handling of organolithium compounds in the laboratory". Chemical Health and Safety. 9 (3): 6–11. doi:10.1016/S1074-9098(02)00295-2. ISSN 1074-9098.
  • Gellert, H; Ziegler, K. (1950). "Organoalkali compounds. XVI. The thermal stability of lithium alkyls". Liebigs Ann. Chem. 567: 179–185. doi:10.1002/jlac.19505670110.
  • Juaristi, E.; Martínez-Richa, A.; García-Rivera, A.; Cruz-Sánchez, J. S. (1983). "Use of 4-Biphenylmethanol, 4-Biphenylacetic Acid and 4-Biphenylcarboxylic Acid/Triphenylmethane as Indicators in the Titration of Lithium Alkyls. Study of the Dianion of 4-Biphenylmethanol". The Journal of Organic Chemistry. 48 (15): 2603–2606. doi:10.1021/jo00163a038.
  • Stanetty, P.; Koller, H.; Mihovilovic, M. (1992). "Directed Ortho-Lithiation of Phenylcarbamic Acid 1,l-Dimethylethyl Ester (N-Boc-aniline). Revision and Improvements". J. Org. Chem. 57 (25): 6833–6837. doi:10.1021/jo00051a030.

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

organicchemistrydata.org

scripps.edu

tamu.edu

chem.tamu.edu

wiley.com

onlinelibrary.wiley.com

worldcat.org

search.worldcat.org

  • Eisch, John J. (2002). "Henry Gilman: American Pioneer in the Rise of Organometallic Chemistry in Modern Science and Technology†". Organometallics. 21 (25): 5439–5463. doi:10.1021/om0109408. ISSN 0276-7333.
  • Weiss, Erwin (November 1993). "Structures of Organo Alkali Metal Complexes and Related Compounds". Angewandte Chemie International Edition in English. 32 (11): 1501–1523. doi:10.1002/anie.199315013. ISSN 0570-0833.
  • Schwindeman, James A.; Woltermann, Chris J.; Letchford, Robert J. (2002). "Safe handling of organolithium compounds in the laboratory". Chemical Health and Safety. 9 (3): 6–11. doi:10.1016/S1074-9098(02)00295-2. ISSN 1074-9098.