Pure and Applied Chemistry

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• Claridge Timothy D.W., Davies Stephen G., Kruchinin Dennis, Odell Barbara, Roberts Paul M., Russell Angela J., Thomson James E., Toms Steven M.: Solution phase structures of enantiopure and racemic lithium N-benzyl-N-(α-methylbenzyl)amide in THF: low temperature 6Li and 15N NMR spectroscopic studies. Tetrahedron: Asymmetry 2013, 24, 947. <http://dx.doi.org/10.1016/j.tetasy.2013.07.001>
• 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>
• Andrews Philip C., Blair Victoria L., Koutsaplis Magdaline, Thompson Christopher D.: Anion Rearrangements of Alkali Metal Complexes of the Chiral Amine (S)-N-α-(Methylbenzyl)phenylallylamine: Structural and Solution Insights. Organometallics 2012, 31, 8135. <http://dx.doi.org/10.1021/om300747w>
• 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>
• Stivala Craig E., Zakarian Armen: Highly Enantioselective Direct Alkylation of Arylacetic Acids with Chiral Lithium Amides as Traceless Auxiliaries. J Am Chcm Soc 2011, 133, 11936. <http://dx.doi.org/10.1021/ja205107x>
• SIMPKINS N. S.: ChemInform Abstract: Recent Advances in Asymmetric Synthesis Using Chiral Lithium Amide Bases. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199643274>
• Studte Christopher, Breit Bernhard: Zink‐katalysierte enantiospezifische sp³‐sp³‐Kreuzkupplung von α‐Hydroxyestertriflaten mit Grignard‐Reagentien. Angew Chem 2008, 120, 5531. <http://dx.doi.org/10.1002/ange.200800733>
• Studte Christopher, Breit Bernhard: Zinc‐Catalyzed Enantiospecific sp³–sp³ Cross‐Coupling of α‐Hydroxy Ester Triflates with Grignard Reagents. Angew Chem Int Ed 2008, 47, 5451. <http://dx.doi.org/10.1002/anie.200800733>
• Koch Christian, Görls Helmar, Westerhausen Matthias: 8-Amidoquinoline, 8-(Trialkylsilylamido)quinoline, 2-Pyridylmethylamide, and (2-Pyridylmethyl)(trialkylsilyl)amide Complexes of Gallium. Z anorg allg Chem 2008, 634, 1365. <http://dx.doi.org/10.1002/zaac.200800088>
• 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>
• Ma Lili, Williard Paul G.: Synthesis of polymer-supported chiral lithium amide bases and application in asymmetric deprotonation of prochiral cyclic ketones. Tet Asymm 2006, 17, 3021. <http://dx.doi.org/10.1016/j.tetasy.2006.11.011>
• Aggarwal Varinder K., Olofsson Berit: Enantioselective α-Arylation of Cyclohexanones with Diaryl Iodonium Salts: Application to the Synthesis of (−)-Epibatidine. Angew Chem 2005, 117, 5652. <http://dx.doi.org/10.1002/ange.200501745>
• Aggarwal Varinder K., Olofsson Berit: Enantioselective α-Arylation of Cyclohexanones with Diaryl Iodonium Salts: Application to the Synthesis of (−)-Epibatidine. Angew Chem Int Ed 2005, 44, 5516. <http://dx.doi.org/10.1002/anie.200501745>
• Sott Richard, Granander Johan, Williamson Carl, Hilmersson Göran: Kinetic and NMR Spectroscopic Studies of Chiral Mixed Sodium/Lithium Amides Used for the Deprotonation of Cyclohexene Oxide. Chem Eur J 2005, 11, 4785. <http://dx.doi.org/10.1002/chem.200500121>
• 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>
• Chiu Pauline, Zhang Xiaomei, Ko Rebecca Y.Y: Desymmetrizations of meso oxabicyclic compounds by asymmetric C–H insertion. Tetrahetron Lett 2004, 45, 1531. <http://dx.doi.org/10.1016/j.tetlet.2003.12.055>
• 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>
• 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>
• 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>
• Pettersen Daniel, Amedjkouh Mohamed, Nilsson Lill Sten O., Ahlberg Per: On the novel function of the additive DBU. Catalytic stereoselective deprotonation by a mixed dimer of lithiated DBU and a chiral lithium amide. J Chem Soc Perkin Trans 2 2002, 1397. <http://dx.doi.org/10.1039/b205618f>
• 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>
• Amedjkouh Mohamed, Pettersen Daniel, Nilsson Lill Sten O., Davidsson Öjvind, Ahlberg Per: A Novel Mixed Dimer of a Norephedrine-Derived Chiral Lithium Amide and 2-Lithium-1-methylimidazole, and Catalytic Enantioselective Deprotonation of Cyclohexene Oxide. Chem Eur J 2001, 7, 4368. <http://dx.doi.org/10.1002/1521-3765(20011015)7:20<4368::AID-CHEM4368>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>
• Magnus Philip, Bailey James M., Porter Michael J.: Application of the β-azidonation reaction to the enantioselective synthesis of the lycorane Amaryllidaceae alkaloids. Tetrahedron 1999, 55, 13927. <http://dx.doi.org/10.1016/S0040-4020(99)00850-9>
• 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>
• Magnus Philip, Sebhat Iyassu K.: Application of the β-azidonation reaction to the synthesis of the antitumor alkaloid (+)-pancratistatin. Tetrahedron 1998, 54, 15509. <http://dx.doi.org/10.1016/S0040-4020(98)00975-2>
• Hoppe Dieter, Hense Thomas: Enantioselektive Synthese mit Lithium/(−)-Spartein-Carbanion-Paaren. Angew Chem 1997, 109, 2376. <http://dx.doi.org/10.1002/ange.19971092105>
• 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>
• 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>