Pure and Applied Chemistry

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• E. Denmark Scott, K. Marble Lyndon: Asymmetric Construction of Quaternary Stereogenic Centers via Auxiliary-Based SN2’ Reactions: A Case of 1,7-Relative Stereogenesis. HETEROCYCLES 2014, 88, 559. <http://dx.doi.org/10.3987/COM-13-S(S)82>
• Fujioka Hiromichi, Yahata Kenzo, Hamada Tomohito, Kubo Ozora, Okitsu Takashi, Sawama Yoshinari, Ohnaka Takuya, Maegawa Tomohiro, Kita Yasuyuki: Reaction of Acetals with Various Carbon Nucleophiles under Non-Acidic Conditions: CC Bond Formation via a Pyridinium-Type Salt. Chem —Asian J 2012, 7, 367. <http://dx.doi.org/10.1002/asia.201100812>
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• Rousseau Géraldine, Breit Bernhard: Removable Directing Groups in Organic Synthesis and Catalysis. Angew Chem Int Ed 2011, 50, 2450. <http://dx.doi.org/10.1002/anie.201006139>
• Chirale cyclische Acetale in der Synthese. Nachr Chem Tech Lab 2010, 36, 1212. <http://dx.doi.org/10.1002/nadc.19880361108>
• García Ruano José Luis, Marcos Vanesa, Alemán José: Configurational Control of Benzyl Carbanion-Copper Complexes by Sulfinyl Groups: Synthesis of Optically Pure Allenes with Central and Axial Chirality. Angew. Chem. 2008, 120, 6942. <http://dx.doi.org/10.1002/ange.200802158>
• García Ruano José Luis, Marcos Vanesa, Alemán José: Configurational Control of Benzyl Carbanion-Copper Complexes by Sulfinyl Groups: Synthesis of Optically Pure Allenes with Central and Axial Chirality. Angew Chem Int Ed 2008, 47, 6836. <http://dx.doi.org/10.1002/anie.200802158>
• Falciola Caroline A., Alexakis Alexandre: Copper-Catalyzed Asymmetric Allylic Alkylation. Eur J Org Chem 2008, 2008, 3765. <http://dx.doi.org/10.1002/ejoc.200800025>
• Krause Norbert, Hoffmann-Röder Anja: Synthesis of allenes with organometallic reagents. Tetrahedron 2004, 60, 11671. <http://dx.doi.org/10.1016/j.tet.2004.09.094>
• Nishikawa Toshihiro, Shinokubo Hiroshi, Oshima Koichiro: Regioselective Allylmetalation of Allenes with Tetraallylmanganate or Allylmagnesium Chloride under MnCl₂ Catalysis. Org Lett 2003, 5, 4623. <http://dx.doi.org/10.1021/ol035793j>
• Krause Norbert, Purpura Martin: „Remote Stereocontrol“ in der Organokupferchemie: hoch enantioselektive Synthese von Vinylallenen durch 1,5-Substitution von Eninacetaten. Angew Chem 2000, 112, 4512. <http://dx.doi.org/10.1002/1521-3757(20001201)112:23<4512::AID-ANGE4512>3.0.CO;2-5>
• Krause Norbert, Purpura Martin: “Remote Stereocontrol” in Organocopper Chemistry: Highly Enantioselective Synthesis of Vinylallenes by 1,5-Substitution of Enyne Acetates. Angew Chem 2000, 39, 4355. <http://dx.doi.org/10.1002/1521-3773(20001201)39:23<4355::AID-ANIE4355>3.0.CO;2-C>
• Purpura Martin, Krause Norbert: Regio- and Stereoselective Synthesis of Vinylallenes by 1,5-(SN′′)-Substitution of Enyne Acetates and Oxiranes with Organocuprates. Eur J Org Chem 1999, 1999, 267. <http://dx.doi.org/10.1002/(SICI)1099-0690(199901)1999:1<267::AID-EJOC267>3.0.CO;2-V>
• Krause Norbert, Gerold Andreas: Regio- und stereoselektive Synthesen mit Organokupferreagentien. Angew Chem 1997, 109, 194. <http://dx.doi.org/10.1002/ange.19971090304>
• Caló Vincenzo, Nacci Angelo, Fiandanese Vito: Copper-mediated regio- and enantio-selective cross-coupling of heterocyclic allyl sulphides with organomagnesium compounds: A case of 1,7-relative stereogenesis. Tetrahedron 1996, 52, 10799. <http://dx.doi.org/10.1016/0040-4020(96)00601-1>
• Caballero Mercedes, García-Valverde María, Pedrosa Rafael, Vicente Martina: Elimination versus diastereoselective alkylation in homochiral 2-(β-ethoxy carbonyl) acetals. Tet Asymm 1996, 7, 219. <http://dx.doi.org/10.1016/0957-4166(95)00438-6>
• Alexakis Alexandre, Mhamdi Farida, Lagasse Franz, Mangeney Pierre: Asymmetric cleavage of chiral α,β-ethylenic acetals by organolithium reagents. Tet Asymm 1996, 7, 3343. <http://dx.doi.org/10.1016/S0957-4166(96)00438-7>
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• Posner Gary H., Shulman-Roskes Ellen M., Oh Chang Ho, Carry Jean-Christophe, Green Julianne V., Clark A.Brian, Dai Haiyan, Anjeh Tizah E.N.: BF3·OEt2 promotes fast, mild, clean and regioselective dehydration of tertiary alcohols. Tetrahetron Lett 1991, 32, 6489. <http://dx.doi.org/10.1016/0040-4039(91)80200-P>
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