Pure and Applied Chemistry

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• Harrison-Marchand Anne, Mongin Florence: Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 1. Structural Data. Chem. Rev. 2013, 113, 7470. <http://dx.doi.org/10.1021/cr300295w>
• Mongin Florence, Harrison-Marchand Anne: Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 2. Syntheses and Reactivities of Homo/HeteroMAAs. Chem. Rev. 2013, 113, 7563. <http://dx.doi.org/10.1021/cr3002966>
• Kumar Varun, Pal Anang, Khatik Gopal L., Bhattacharya Suman, Nair Vipin A.: Additive controlled, stereoselective benzylation of 2-thioxotetrahydropyrimidin-4(1H)-ones via chiral induction from a remote stereocenter. Tetrahedron: Asymmetry 2012, 23, 434. <http://dx.doi.org/10.1016/j.tetasy.2012.04.002>
• Rönnholm Petra, Gräfenstein Jürgen, Norrby Per-Ola, Hilmersson Göran, Nilsson Lill Sten O.: A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide. Biomol Chem 2012, 10, 2807. <http://dx.doi.org/10.1039/c2ob06910e>
• Sasaki Michiko, Kondo Yasuhiro, Kawahata Masatoshi, Yamaguchi Kentaro, Takeda Kei: Enantioselective Synthesis of Siloxyallenes from Alkynoylsilanes by Reduction and a Brook Rearrangement and Their Subsequent Trapping in a [4+2] Cycloaddition. angew chemie 2011, 123, 6499. <http://dx.doi.org/10.1002/ange.201102430>
• Sasaki Michiko, Kondo Yasuhiro, Kawahata Masatoshi, Yamaguchi Kentaro, Takeda Kei: Enantioselective Synthesis of Siloxyallenes from Alkynoylsilanes by Reduction and a Brook Rearrangement and Their Subsequent Trapping in a [4+2] Cycloaddition. Angewandte Chemie-Int Ed 2011, 50, 6375. <http://dx.doi.org/10.1002/anie.201102430>
• Lazny Ryszard, Wolosewicz Karol, Zielinska Paulina, Urbanczyk-Lipkowska Zofia, Kalicki Przemyslaw: Diastereo- and enantioselective aldol reaction of granatanone (pseudopelletierine). Tedrahedron 2011, 67, 9433. <http://dx.doi.org/10.1016/j.tet.2011.09.096>
• Denmark Scott E., Gould Nathan D., Wolf Larry M.: A Systematic Investigation of Quaternary Ammonium Ions as Asymmetric Phase-Transfer Catalysts. Synthesis of Catalyst Libraries and Evaluation of Catalyst Activity. J Org Chem 2011, 76, 4260. <http://dx.doi.org/10.1021/jo2005445>
• KOGA K.: ChemInform Abstract: Asymmetric Synthesis Mediated by Chiral Ligands. ChemInform 2010, 25, no. <http://dx.doi.org/10.1002/chin.199441294>
• Dietinger Christine E., Banwell Martin G., Garson Mary J., Willis Anthony C.: Chemoenzymatic and enantioselective assembly of the (1α,3aβ,6α,7aβ)-octahydro-1,6-methano-1H-indene framework associated with 2-isocyanoallopupukeanane: validation of a new synthetic strategy and the identification of enantiomeric switching regimes. Tetrahedron 2010, 66, 5250. <http://dx.doi.org/10.1016/j.tet.2010.04.056>
• Urabe Daisuke, Inoue Masayuki: Total syntheses of sesquiterpenes from Illicium species. Tetrahedron 2009, 65, 6271. <http://dx.doi.org/10.1016/j.tet.2009.06.010>
• Montaña Ángel M., Ponzano Stefano, Kociok-Köhn Gabriele, Font-Bardia Mercè, Solans Xavier: Versatile Methodology to Synthesize Oxygen-Bridged Nine- and Ten-Membered Cycloalkanes by the Hypoiodite Reaction. Eur J Org Chem 2007, 2007, 4383. <http://dx.doi.org/10.1002/ejoc.200700172>
• Xiao Ying, Jung Dawoon, Gund Tamara, Malhotra Sanjay V.: An experimental and theoretical study of the enantioselective deprotonation of cyclohexene oxide with isopinocampheyl-based chiral lithium amides. J Mol Model 2006, 12, 681. <http://dx.doi.org/10.1007/s00894-006-0114-2>
• Andrews Philip C., Calleja Simone, Maguire Melissa: Crystal structures and unusual solution behaviour of diastereomeric aluminium and gallium complexes of chiral amines [Me3M·RR*NH]. J Polyhedron 2006, 25, 1625. <http://dx.doi.org/10.1016/j.poly.2005.10.028>
• Seki Atsushi, Ishiwata Fusae, Takizawa Youichi, Asami Masatoshi: Crossed aldol reaction using cross-linked polymer-bound lithium dialkylamide. Tetrahedron 2004, 60, 5001. <http://dx.doi.org/10.1016/j.tet.2004.04.026>
• Bassindale Martin J., Crawford James J., Henderson Kenneth W., Kerr William J.: Application of polydentate chiral amines within magnesium-mediated asymmetric deprotonation reactions. Tetrahetron Lett 2004, 45, 4175. <http://dx.doi.org/10.1016/j.tetlet.2004.03.113>
• Malhotra Sanjay V: Lithium diisopinocampheylamide: a new and highly effective chiral catalyst in the enantioselective deprotonation of meso-epoxides. Tet Asymm 2003, 14, 645. <http://dx.doi.org/10.1016/S0957-4166(03)00080-6>
• Johansson Anna, Abrahamsson Peter, Davidsson Öjvind: Solid-phase supported chiral lithium amides used in deprotonation reactions. Tet Asymm 2003, 14, 1261. <http://dx.doi.org/10.1016/S0957-4166(03)00280-5>
• Andrews Philip C., Calleja Simone M., Maguire Melissa, Nichols Peter J.: A 1,3-Sigmatropic Rearrangement Revealed in the Solid and Solution State Structures of a Chiral Sodium 1-Azaallyl Complex Derived from (S)-N-(α-Methylbenzyl)allylamine. Eur J Inorg Chem 2002, 2002, 1583. <http://dx.doi.org/10.1002/1099-0682(200207)2002:7<1583::AID-EJIC1583>3.0.CO;2-J>
• Eames Jason: Recent Developments in Enantioselective Deprotonation Mediated by Sub-Stoichiometric Quantities of Chiral Bases. Eur J Org Chem 2002, 2002, 393. <http://dx.doi.org/10.1002/1099-0690(20022)2002:3<393::AID-EJOC393>3.0.CO;2-F>
• Majewski Marek, Wang Fan: Are there concentration effects in enantioselective deprotonation of cyclic ketones?. Tetrahedron 2002, 58, 4567. <http://dx.doi.org/10.1016/S0040-4020(02)00363-0>
• Henderson Kenneth W, Kerr William J, Moir Jennifer H: Magnesium amide base-mediated enantioselective deprotonation processes. Tetrahedron 2002, 58, 4573. <http://dx.doi.org/10.1016/S0040-4020(02)00364-2>
• Seki Atsushi, Asami Masatoshi: Catalytic enantioselective rearrangement of meso-epoxides mediated by chiral lithium amides in the presence of excess cross-linked polymer-bound lithium amides. Tetrahedron 2002, 58, 4655. <http://dx.doi.org/10.1016/S0040-4020(02)00371-X>
• Hunt Kevin W., Grieco Paul A.: Oxabicyclo[3.2.1]octenes in Organic Synthesis:  Direct Ring Opening of Oxabicyclo[3.2.1] Ring Systems with Diisobutylaluminum Hydride and a Silyl Ketene AcetalSynthesis of the Chiral C(19)−C(26) and C(27)−C(32) Fragments of Scytophycin C. Org Lett 2002, 4, 245. <http://dx.doi.org/10.1021/ol010253c>
• Honda Toshio, Kimura Nobuaki: Enantioselective Deprotonation of meso-Cycloheptanone Derivative:  Application to the Synthesis of a Potential Intermediate for Pseudomonic Acid B. Org Lett 2002, 4, 4567. <http://dx.doi.org/10.1021/ol027192i>
• Asami Masatoshi, Seki Atsushi: An Intriguing Effect of Polymer-Bound Lithium Amides in Catalytic Enantioselective Rearrangement of meso-Epoxides Mediated by Chiral Lithium Amides. Chem Lett 2002, 160. <http://dx.doi.org/10.1246/cl.2002.160>
• Seebach Dieter, Beck Albert K., Heckel Alexander: TADDOLe, ihre Derivate und Analoga – vielseitige chirale Hilfsstoffe. Angew Chem 2001, 113, 96. <http://dx.doi.org/10.1002/1521-3757(20010105)113:1<96::AID-ANGE96>3.0.CO;2-B>
• Hilmersson Göran, Malmros Birgitta: Mixed Dimer and Mixed Trimer Complexes ofnBuLi and a Chiral Lithium Amide. Chem Eur J 2001, 7, 337. <http://dx.doi.org/10.1002/1521-3765(20010119)7:2<337::AID-CHEM337>3.0.CO;2-I>
• Seebach Dieter, Beck Albert K., Heckel Alexander: TADDOLs, Their Derivatives, and TADDOL Analogues: Versatile Chiral Auxiliaries. Angewandte Chemie-Int Ed 2001, 40, 92. <http://dx.doi.org/10.1002/1521-3773(20010105)40:1<92::AID-ANIE92>3.0.CO;2-K>
• TORIYAMA Masaharu, TOKUTAKE Norio, KOGA Kenji: Stereoselective Reactions. XXXIII. Design and Synthesis of Chiral Bidentate Amines Having a Bulky Group on the Chiral Carbon. Chem Pharm Bull 2001, 49, 330. <http://dx.doi.org/10.1248/cpb.49.330>
• TORIYAMA Masaharu, SUGASAWA Keizo, MOTOHASHI Shigeyasu, TOKUTAKE Norio, KOGA Kenji: Stereoselective Reactions. XXXIV. Enantioselective Deprotonation of Prochiral 4-Substituted Cyclohexanones Using Chiral Bidentate Lithium Amides Having a Bulky Group Instead of a Phenyl Group on the Chiral Carbon. Chem Pharm Bull 2001, 49, 468. <http://dx.doi.org/10.1248/cpb.49.468>
• Arvidsson Per I., Davidsson Öjvind: 6Li and15N NMR Data as a Probe for the Influence of Solvent and Intramolecular Solvation on the Solution-State Structures of Chiral Lithium Amides. Angew Chem 2000, 112, 1527. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000417)112:8<1527::AID-ANGE1527>3.0.CO;2-B>
• Yamashita Yasuhiro, Odashima Kazunori, Koga Kenji: Construction of chiral quaternary carbon centers by asymmetric alkylation of achiral lithium enolates mediated by chiral tetradentate ligands: Stoichiometric and catalytic approaches. Tetrahetron Lett 1999, 40, 2803. <http://dx.doi.org/10.1016/S0040-4039(99)00299-3>
• Lucet Denis, Le Gall Thierry, Mioskowski Charles: Die Chemie vicinaler Diamine. Angew Chem 1998, 110, 2724. <http://dx.doi.org/10.1002/(SICI)1521-3757(19981002)110:19<2724::AID-ANGE2724>3.0.CO;2-4>
• O’Brien Peter: Recent advances in asymmetric synthesis using chiral lithium amide bases. J Chem Soc Perkin Trans 1 1998, 1439. <http://dx.doi.org/10.1039/a705961e>
• Arvidsson Per I, Hansson Maria, Khan Agha Zul-Qarnain, Ahlberg Per: Solvent-induced stereospecific isomerization of an allylic alcohol to a homoallylic alcohol catalyzed by a chiral lithium amide. Can J Chem 1998, 76, 795. <http://dx.doi.org/10.1139/v98-052>
• Hoppe Dieter, Hense Thomas: Enantioselektive Synthese mit Lithium/(−)-Spartein-Carbanion-Paaren. Angew Chem 1997, 109, 2376. <http://dx.doi.org/10.1002/ange.19971092105>
• Sato Daisaku, Kawasaki Hisashi, Shimada Ichio, Arata Yoji, Okamura Kimio, Date Tadamasa, Koga Kenji: Stereoselective reactions. 26. Solution structures of chiral bidentate lithium amide in relation to the solvent-dependent enantioselectivities in deprotonation reaction. Tetrahedron 1997, 53, 7191. <http://dx.doi.org/10.1016/S0040-4020(97)00422-5>
• Aoki Kazumasa, Tomioka Kiyoshi, Noguchi Hiroshi, Koga Kenji: Stereoselective reactions. 28. Effects of the alkyl group at the amide nitrogen of chiral bidentate lithium amides on enantioselective deprotonation reaction. Tetrahedron 1997, 53, 13641. <http://dx.doi.org/10.1016/S0040-4020(97)00901-0>
• Yamashita Toyoharu, Sato Daisaku, Kiyoto Taro, Kumar Arvind, Koga Kenji: Stereoselective reactions. 29. Lithium-hydrogen interchange between achiral tridentate lithium amides and chiral bidentate amines. An approach to catalytic enantioselective deprotonation. Tetrahedron 1997, 53, 16987. <http://dx.doi.org/10.1016/S0040-4020(97)10144-2>
• Toriyama Masaharu, Sugasawa Keizo, Shindo Mitsuru, Tokutake Norio, Koga Kenji: Stereochemistry of enantioselective deprotonation of 4-substituted cyclohexanones by chiral bidentate lithium amides. Tetrahetron Lett 1997, 38, 567. <http://dx.doi.org/10.1016/S0040-4039(96)02373-8>
• Nowakowski Marc, Hoffmann H.M.R: Asymmetric synthesis of the C(18)C(24) unit of lasonolide A. Tetrahetron Lett 1997, 38, 1001. <http://dx.doi.org/10.1016/S0040-4039(96)02481-1>
• Ho David E., Betancort Juan M., Woodmansee David H., Larter Martin L., Walsh Patrick J.: Synthesis of new chiral tetradentate sulfonamide based ligands. Tetrahetron Lett 1997, 38, 3867. <http://dx.doi.org/10.1016/S0040-4039(97)00796-X>
• Sugasawa Keizo, Shindo Mitsuru, Noguchi Hiroshi, Koga Kenji: Solution structures of a monodentate chiral lithium amide in the presence of lithium halide. Tetrahetron Lett 1996, 37, 7377. <http://dx.doi.org/10.1016/0040-4039(96)01681-4>
• Yamashita Toyoharu, Sato Daisaku, Kiyoto Taro, Kumar Arvind, Koga Kenji: An approach to catalytic asymmetric deprotonation of 4-substituted cyclohexanones. Tetrahetron Lett 1996, 37, 8195. <http://dx.doi.org/10.1016/0040-4039(96)01859-X>
• Kim Hee-doo: Kinetic resolution of bicyclic ketones by enantioselective deprotonation. Arch Pharm Res 1995, 18, 369. <http://dx.doi.org/10.1007/BF02976336>
• Majewski Marek, Lazny Ryszard, Nowak Pawel: Effect of lithium salts on enantioselective deprotonation of cyclic ketones. Tetrahetron Lett 1995, 36, 5465. <http://dx.doi.org/10.1016/0040-4039(95)01056-N>