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Pure Appl. Chem., 1983, Vol. 55, No. 11, pp. 1749-1758

http://dx.doi.org/10.1351/pac198355111749

Metal enolates in organic synthesis

T. Mukaiyama

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  • Bartoszewicz Agnieszka, Jeżowska Martina M., Laymand Kévin, Möbus Juri, Martín-Matute Belén: Synthesis of β-Hydroxy and β-Amino Ketones from Allylic Alcohols Catalyzed by Ru(η5-C5Ph5)(CO)2Cl. Euro J Inorg Chem 2012, 2012, 1517. <http://dx.doi.org/10.1002/ejic.201101014>
  • Gao Ruili, Yi Chae S.: Catalytic Formation of Silyl Enol Ethers and Its Applications for Aldol-Type Condensation and Aminomethylation Reactions. ACS Catal 2011, 544. <http://dx.doi.org/10.1021/cs200087c>
  • Robertson Bradley D., Hartel Aaron M.: Preparation of silyl enol ethers from acyloin derivatives using silyllithium reagents. Tetrahetron Lett 2008, 49, 2088. <http://dx.doi.org/10.1016/j.tetlet.2008.01.133>
  • Fielding Alistair J, Roberts Brian P: Radical-chain isomerisation of allyl silyl ethers to silyl enol ethers in the presence of thiols as polarity reversal catalysts. Tetrahetron Lett 2001, 42, 4061. <http://dx.doi.org/10.1016/S0040-4039(01)00630-X>
  • Kodama Yoshitoshi, Yamane Hidefumi, Okumura Masato, Shiro Motoo, Taguchi Takeo: Lewis acid catalyzed aldol-type reaction of 1,1-difluorovinyl methyl ether derivatives. Tetrahedron 1995, 51, 12217. <http://dx.doi.org/10.1016/0040-4020(95)00785-7>
  • Tückmantel Werner: Synthesis of Pyrano[4,3-b]Azepines by [4 + 2] Cycloaddition of Photochemically Generated 3-Alkoxycarbonyl-1,2-Didehydroazepines with Enol Ethers. Liebigs Ann Chem 1994, 1994, 1165. <http://dx.doi.org/10.1002/jlac.199419941205>
  • Beckhaus Rüdiger, Strauß Isabelle, Wagner Trixie: Zum reaktionsverhalten von titanocenvinyliden gegenüber enolisierbaren ketonen: Cp★2Ti(CHCH2)(OC( CH2)C6H11) -ein enolat mit ungewöhnlich gestrecktem TiOC-Winkel. J Organomet Chem 1994, 464, 155. <http://dx.doi.org/10.1016/0022-328X(94)87269-4>
  • Gibson Charles P., Bem David S.: (η5-C5Me5)2(Me)TiOC(Me)CH2: titanum enolate or titanum alkoxide?. J Organomet Chem 1991, 414, 23. <http://dx.doi.org/10.1016/0022-328X(91)83238-Y>
  • Palomo Caludio, Aizpurua Jesus M., Aurrejoetxea Natalia, Concepción López M.: Regiocontrol synthesis of β-trimetylsilyloxy carbonyl compounds through an aldol-grignard elaboration sequence. Tetrahetron Lett 1991, 32, 2525. <http://dx.doi.org/10.1016/S0040-4039(00)74372-3>
  • Maruoka Keiji, Hirayama Naoki, Yamamoto Hisashi: A new preparative method for various metal enolates. J Polyhedron 1990, 9, 223. <http://dx.doi.org/10.1016/S0277-5387(00)80572-0>
  • Hegedus Louis S.: Transition metals in organic synthesis annual survey covering the year 1984. J Organomet Chem 1986, 298, 207. <http://dx.doi.org/10.1016/0022-328X(86)82006-X>
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  • Dubois Jacques-Emile, Axiotis Georges, Bertounesque Emmanuel: Chromium (II) chloride : a new reagent for cross-aldol reactions. Tetrahetron Lett 1985, 26, 4371. <http://dx.doi.org/10.1016/S0040-4039(00)98737-9>
  • Welch John T., Seper Karl W.: Diastereoselectivity in the directed aldol reactions of 1-fluoro-3,3-dimethyl-butanone enolates and enol silyl ethers. Tetrahetron Lett 1984, 25, 5247. <http://dx.doi.org/10.1016/S0040-4039(01)81575-6>
  • Dubois Jacques-Emile, Axiotis Georges, Bertounesque Emmanuel: Ketene bis(trimethylsilyl) acetals. Cross-aldol condensation with aldehydes. Stereochemistry of the reaction. Tetrahetron Lett 1984, 25, 4655. <http://dx.doi.org/10.1016/S0040-4039(01)91225-0>