Pure and Applied Chemistry

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• Bartoli Giuseppe, Bosco Marcella, Cimarelli Cristina, Dalpozzo Renato, De Munno Giovanni, Palmieri Gianni: Stereoselective alkylation of cyclic and acyclic chiral β-enamino ketones lithium dianions: synthesis of either (R)- or (S)-chiral 1,3-diketones. Tet Asymm 1993, 4, 1651. <http://dx.doi.org/10.1016/S0957-4166(00)80373-0>
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• Takahashi Takashi, Shimizu Katsuya, Doi Takayuki, Tsuji Jiro, Yamamoto Keiji: Efficient approach to the oppolzer-kametani intermediate for estrone methyl ether using the conjugate addition-enolate methylation of the cyclopentenone containing an α-appended benzocyclobutane moiety. Tetrahetron Lett 1989, 30, 4999. <http://dx.doi.org/10.1016/S0040-4039(01)80565-7>
• Glaser Rainer, Streitwieser Andrew: A MNDO-study of solvent free and solvated dimeric lithium ion pairs of acetaldoxime. Models for dimeric aggregates of lithiated oxime ethers. Journal of Molecular Structure: THEOCHEM 1988, 163, 19. <http://dx.doi.org/10.1016/0166-1280(88)80377-4>
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• Padwa Albert, Kline Donald N., Perumattam John: Isoxazoline oxidation. An efficient method for the preparation of α,β-unsaturated carbonyl compounds. Tetrahetron Lett 1987, 28, 913. <http://dx.doi.org/10.1016/S0040-4039(00)95872-6>
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• Durman John, Elliott Jason, McElroy Andrew B., Warren Stuart: Regiospecific synthesis of enones α-(phenylthio)-ketones: 2,5-dimethyl-4-hexen-3-one, -6-methyl-2-hepten-4-one, -7-methyl-4-octen-3-one, and ar-turmerone. Tetrahetron Lett 1983, 24, 3927. <http://dx.doi.org/10.1016/S0040-4039(00)94317-X>
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• Takahashi Takashi, Hori Kimihiko, Tsuji Jiro: Regiospecific carbon—carbon bond formation at α and β positions in cyclic ketones via double Michael addition to α-methylene-β-alkoxy cyclic ketone. Tetrahetron Lett 1981, 22, 119. <http://dx.doi.org/10.1016/0040-4039(81)80164-5>
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• Reetz Manfred T., Maier Wilhelm F., Chatziiosifidis Ioannis, Giannis Athanassios, Heimbach Horst, Löwe Ursula: Lewis-Säure-bedingte α-Alkylierung von Carbonylverbindungen, VII. Regio- und positionsspezifische α-tert-Alkylierung von Ketonen. Chem Ber 1980, 113, 3741. <http://dx.doi.org/10.1002/cber.19801131208>
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