Οργανολιθιακές ενώσεις (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Οργανολιθιακές ενώσεις" in Greek language version.

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33doi.org

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acs.org

pubs.acs.org

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].»]. JACS 105: 5320–5324. doi:10.1021/ja00354a022. http://pubs.acs.org/doi/pdf/10.1021/ja00354a022.
Reich, H.J; Green, D.P (1989). «Spectroscopic and Reactivity Studies of Lithium Reagent - HMPA Complexes». JACS 111: 8729–8731. doi:10.1021/ja00205a030. http://pubs.acs.org/doi/pdf/10.1021/ja00205a030.
Williard, P.G; Nichols, M.A (1993). «Solid-state structures of n-butyllithium-TMEDA, -THF, and -DME complexes». JACS 115: 1568–1572. doi:10.1021/ja00057a050. http://pubs.acs.org/doi/pdf/10.1021/ja00057a050.
Cohen, T; Bhupathy. M (1989). «Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers». Acc. Chem. Res. 22: 152–161. doi:10.1021/ar00160a006. http://pubs.acs.org/doi/pdf/10.1021/ar00160a006.
Snieckus, V (1990). «Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics». Chem. Rev. 90: 879–933. doi:10.1021/cr00104a001. http://pubs.acs.org/doi/pdf/10.1021/cr00104a001.

archive.org

Reich, Hans J. (2013). «Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms». Chemical Reviews 113: 7130–7178. doi:10.1021/cr400187u. PMID 23941648. https://archive.org/details/sim_chemical-reviews_2013-09_113_9/page/7130.
Streiwieser, A. (2009). «Perspectives on Computational Organic Chemistry». J. Org. Chem. 74: 4433–4446. doi:10.1021/jo900497s. PMC 2728082. https://archive.org/details/sim_journal-of-organic-chemistry_2009-06-19_74_12/page/n9.
Sekiguchi, Akira. (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. https://archive.org/details/sim_coordination-chemistry-reviews_2000-12_210/page/11.
Si-Fodil, M. (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: 8975–8978. doi:10.1016/S0040-4039(98)02031-0. https://archive.org/details/sim_tetrahedron-letters_1998-12-03_39_49/page/n71.

doi.org

dx.doi.org

Wu, G.; Huang, M. (2006). «Organolithium Reagents in Pharmaceutical Asymmetric Processes». Chem. Rev. 106: 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.
Reich, Hans J. (2013). «Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms». Chemical Reviews 113: 7130–7178. doi:10.1021/cr400187u. PMID 23941648. https://archive.org/details/sim_chemical-reviews_2013-09_113_9/page/7130.
Strohmann, C (2009). «Structure Formation Principles and Reactivity of Organolithium Compounds.». Chem. Eur. J. 15: 3320–3334. doi:10.1002/chem.200900041. http://onlinelibrary.wiley.com/store/10.1002/chem.200900041/asset/3320_ftp.pdf?v=1&t=hnc3zl4k&s=90cd763c5affe82ca5d8208a75ea074deede3187. ^{[νεκρός σύνδεσμος]}
Streiwieser, A. (2009). «Perspectives on Computational Organic Chemistry». J. Org. Chem. 74: 4433–4446. doi:10.1021/jo900497s. PMC 2728082. https://archive.org/details/sim_journal-of-organic-chemistry_2009-06-19_74_12/page/n9.
Bickelhaupt, F. M. (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: 965–980. doi:10.1021/ct050333s.
Weiss, Erwin (November 1993). «Structures of Organo Alkali Metal Complexes and Related Compounds» (στα αγγλικά). Angewandte Chemie International Edition in English 32 (11): 1501–1523. doi:10.1002/anie.199315013. ISSN 0570-0833. https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.199315013.
Fraenkel. G (1995). «The carbon-lithium bond in monomeric arllithium: Dynamics of exchange, relaxation and rotation». J. Am. Chem. Soc. 117: 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].»]. JACS 105: 5320–5324. doi:10.1021/ja00354a022. http://pubs.acs.org/doi/pdf/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.
Collum, D.B. (2007). «Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis». Angew. Chem. Int. Ed. 49: 3002–3017. doi:10.1002/anie.200603038.
Sekiguchi, Akira. (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. https://archive.org/details/sim_coordination-chemistry-reviews_2000-12_210/page/11.
Collum, D. B. (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: 7743–7747. doi:10.1021/jo801532d.
Reich, H. J. (1998). «Aggregation and reactivity of phenyllithium solutions». J. Am. Chem. Soc. 120: 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: 1805–1810. doi:10.1021/ja00293a001.
Reich, H. J. (2012). «What's going on with these lithium reagents». J. Org. Chem. 77: 5471–5491. doi:10.1021/jo3005155.
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: 11719–11725. doi:10.1021/ja8017187. PMID 18686951.
Collum, D. B. (2007). «Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis». Angew. Chem. Int. Ed. 46: 3002–3017. doi:10.1002/anie.200603038.
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. http://ac.els-cdn.com/0022328X68800919/1-s2.0-0022328X68800919-main.pdf?_tid=7e210432-400f-11e3-ae82-00000aab0f6b&acdnat=1382992283_758e6f8c4a5075990e017ab0a5c00770.
Reich, H.J; Green, D.P (1989). «Spectroscopic and Reactivity Studies of Lithium Reagent - HMPA Complexes». JACS 111: 8729–8731. doi:10.1021/ja00205a030. http://pubs.acs.org/doi/pdf/10.1021/ja00205a030.
Williard, P.G; Nichols, M.A (1993). «Solid-state structures of n-butyllithium-TMEDA, -THF, and -DME complexes». JACS 115: 1568–1572. doi:10.1021/ja00057a050. http://pubs.acs.org/doi/pdf/10.1021/ja00057a050.
Collum, D.B. (1992). «Is N,N,N,N-Tetramethylethylenediamine a Good Ligand for Lithium?». Acc. Chem. Res. 25: 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: 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.». Angew. Chem. Int. Ed. 27: 1624–1654. doi:10.1002/anie.198816241. http://onlinelibrary.wiley.com/store/10.1002/anie.198816241/asset/198816241_ftp.pdf?v=1&t=hnc87p5u&s=0a5c03a2a79fd94ea5461e768687e4b5fc7d4f3b. ^{[νεκρός σύνδεσμος]}
Si-Fodil, M. (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: 8975–8978. doi:10.1016/S0040-4039(98)02031-0. https://archive.org/details/sim_tetrahedron-letters_1998-12-03_39_49/page/n71.
Cohen, T; Bhupathy. M (1989). «Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers». Acc. Chem. Res. 22: 152–161. doi:10.1021/ar00160a006. http://pubs.acs.org/doi/pdf/10.1021/ar00160a006.
Snieckus, V (1990). «Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics». Chem. Rev. 90: 879–933. doi:10.1021/cr00104a001. http://pubs.acs.org/doi/pdf/10.1021/cr00104a001.
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

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.
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.
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.
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.
Baskara, D.· Muller, 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.

els-cdn.com

ac.els-cdn.com

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. http://ac.els-cdn.com/0022328X68800919/1-s2.0-0022328X68800919-main.pdf?_tid=7e210432-400f-11e3-ae82-00000aab0f6b&acdnat=1382992283_758e6f8c4a5075990e017ab0a5c00770.

nih.gov

ncbi.nlm.nih.gov

Wu, G.; Huang, M. (2006). «Organolithium Reagents in Pharmaceutical Asymmetric Processes». Chem. Rev. 106: 2596–2616. doi:10.1021/cr040694k. PMID 16836294.
Reich, Hans J. (2013). «Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms». Chemical Reviews 113: 7130–7178. doi:10.1021/cr400187u. PMID 23941648. https://archive.org/details/sim_chemical-reviews_2013-09_113_9/page/7130.
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: 11719–11725. doi:10.1021/ja8017187. PMID 18686951.

pubmedcentral.nih.gov

Streiwieser, A. (2009). «Perspectives on Computational Organic Chemistry». J. Org. Chem. 74: 4433–4446. doi:10.1021/jo900497s. PMC 2728082. https://archive.org/details/sim_journal-of-organic-chemistry_2009-06-19_74_12/page/n9.
Collum, D. B. (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: 7743–7747. doi:10.1021/jo801532d.

wiley.com

onlinelibrary.wiley.com

Strohmann, C (2009). «Structure Formation Principles and Reactivity of Organolithium Compounds.». Chem. Eur. J. 15: 3320–3334. doi:10.1002/chem.200900041. http://onlinelibrary.wiley.com/store/10.1002/chem.200900041/asset/3320_ftp.pdf?v=1&t=hnc3zl4k&s=90cd763c5affe82ca5d8208a75ea074deede3187. ^{[νεκρός σύνδεσμος]}
Weiss, Erwin (November 1993). «Structures of Organo Alkali Metal Complexes and Related Compounds» (στα αγγλικά). Angewandte Chemie International Edition in English 32 (11): 1501–1523. doi:10.1002/anie.199315013. ISSN 0570-0833. https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.199315013.
Seebach, D (1988). «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. 27: 1624–1654. doi:10.1002/anie.198816241. http://onlinelibrary.wiley.com/store/10.1002/anie.198816241/asset/198816241_ftp.pdf?v=1&t=hnc87p5u&s=0a5c03a2a79fd94ea5461e768687e4b5fc7d4f3b. ^{[νεκρός σύνδεσμος]}

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» (στα αγγλικά). Angewandte Chemie International Edition in English 32 (11): 1501–1523. doi:10.1002/anie.199315013. ISSN 0570-0833. https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.199315013.