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Pure Appl. Chem., 1983, Vol. 55, No. 2, pp. 277-282

http://dx.doi.org/10.1351/pac198855020277

Theoretical studies of the stereoselectivities of organic reactions

K. N. Houk

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  • Wolf Larry M., Denmark Scott E.: A Theoretical Investigation on the Mechanism and Stereochemical Course of the Addition of (E)-2-Butenyltrimethylsilane to Acetaldehyde by Electrophilic and Nucleophilic Activation. J. Am. Chem. Soc. 2013, 135, 4743. <http://dx.doi.org/10.1021/ja311889v>
  • Ellwood Paul, Mathlas John P., Fraser Stoddart J., Kohnke Franz H.: Stereoelectronically-programmed molecular ‘lego’ sets. Bull Soc Chim Belges 2010, 97, 669. <http://dx.doi.org/10.1002/bscb.19880970807>
  • Padwa Albert, Prein Michael: Acyclic stereocontrol in [3+2]-cycloadditions of amino acid-derived isomünchnone dipoles. Tetrahedron 1998, 54, 6957. <http://dx.doi.org/10.1016/S0040-4020(98)00339-1>
  • Pale P., Bouquant J., Chuche J., Carrupt P.A., Vogel P.: π-Facial diastereoselection in [4+2]-cycloadditions of 3,4- epoxy-2-methyleneoxolanes with oxadienes: A short synthesis of spiroketals. Tetrahedron 1994, 50, 8035. <http://dx.doi.org/10.1016/S0040-4020(01)85288-1>
  • Starý Ivo, Zajíček Jaroslav, Kočovský Pavel: Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration. Tetrahedron 1992, 48, 7229. <http://dx.doi.org/10.1016/S0040-4020(01)88263-6>
  • Gung Benjamin W., Smith Daniel T., Wolf Mark A.: Evidence for Synclinal Transition State in the Reactions of Aromatic Aldehydes with α-(Alkoxy)allylstannanes. Tetrahedron 1992, 48, 5455. <http://dx.doi.org/10.1016/S0040-4020(01)88299-5>
  • Désert Stéphane, Metzner Patrick, Ramdani Mohamed: Acyclic stereocontrol through the thio-Claisen rearrangement of precursors bearing a chiral centre adjacent to carbon 1. Tetrahedron 1992, 48, 10315. <http://dx.doi.org/10.1016/S0040-4020(01)88336-8>
  • Hünig Siegfried, Marschner Claus: Trimethylsilylcyanid als Umpolungsreagens, XVI: Einfluß der Umpolungsgruppe auf die Diastereoselektivität der nucleophilen Acylierung α-chiraler Carbonylverbindungen. Chem Ber 1989, 122, 1329. <http://dx.doi.org/10.1002/cber.19891220717>
  • Herradón Bernardo, Seebach Dieter: Mono- and Dialkylation of Derivatives of (1R, 2S)-2-Hydroxycyclopentanecarboxylic Acid and -cyclohexanecarboxylic acidvia bicyclic dioxanones: Selective generation of three contiguous stereogenic centers on a cyclohexane ring. HCA 1989, 72, 690. <http://dx.doi.org/10.1002/hlca.19890720410>
  • Kunz Thomas, Reißig Hans-Ulrich: Radical Additions in Aqueous Medium: Direct Synthesis of 5-Allyl-Substituted γ-Lactones from Allylic Bromides/Zinc and Methyl γ-Oxocarboxylates. Liebigs Ann Chem 1989, 1989, 891. <http://dx.doi.org/10.1002/jlac.198919890240>
  • Leanna M.Robert, Martinelli Michael J., Varie David L., Kress Thomas J.: Diastereoselectivity in ergoline synthesis: A face selective epoxidation. Tetrahetron Lett 1989, 30, 3935. <http://dx.doi.org/10.1016/S0040-4039(00)99288-8>
  • Belaj Ferdinand, Huber Stefan, Neier Reinhard: Die röntgenstrukturanalysen von (E)- und (Z)-2-Buten-1,4-diyl-dithiocyanat bei 93 K. HCA 1988, 71, 1235. <http://dx.doi.org/10.1002/hlca.19880710535>
  • Murata Shizuaki, Suzuki Toshiyasu: Cyclization of olefinic alcohol by benzeneselenenyl triflate. Tetrahetron Lett 1987, 28, 4297. <http://dx.doi.org/10.1016/S0040-4039(00)96489-X>
  • Patel Mona, Boger Dale L.: Diels-Alder cycloadditions of rigid dienophiles: A probe for allylic axial substituent control of the pi-facial selectivity in the Diels-Alder reaction. Tetrahetron Lett 1986, 27, 683. <http://dx.doi.org/10.1016/S0040-4039(00)84072-1>
  • Tokles Maritherese, Snyder John K.: Asymmetric oxidation of olefins to vicinal diols with osmium tetroxide. Tetrahetron Lett 1986, 27, 3951. <http://dx.doi.org/10.1016/S0040-4039(00)84881-9>
  • Annunziata Rita, Cinquini Mauro, Cozzi Franco, Raimondi Laura, Restelli Angelo: Stereoselective Synthesis of Masked Amino-polyolsvia Osmylation of 4,5-Dihydro-5-vinylisoxazoles. HCA 1985, 68, 1217. <http://dx.doi.org/10.1002/hlca.19850680518>
  • Calderari Giorgio, Seebach Dieter: AsymmetrischeMichael-Additionen. Stereoselektive Alkylierung chiraler, nicht racemischer Enolate durch Nitroolefine. Herstellung enantiomerenreiner γ-Aminobuttersäure- und Bernsteinsäure-Derivate. HCA 1985, 68, 1592. <http://dx.doi.org/10.1002/hlca.19850680611>
  • Cha J.K., Christ W.J., Kishi Y.: On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical rule. Tetrahedron 1984, 40, 2247. <http://dx.doi.org/10.1016/0040-4020(84)80008-3>
  • McGarvey Glenn J., Kimura Masayuki, Oh Taeboem, Williams J. Michael: Acyclic Stereoselective Synthesis of Carbohydrates. J Carbohydr Chem 1984, 3, 125. <http://dx.doi.org/10.1080/07328308408058813>
  • Cha J.K., Christ W.J., Kishi Y.: On stereochemistry of osmium tetroxide oxidation of allylic alcohol systems: empirical rule. Tetrahetron Lett 1983, 24, 3943. <http://dx.doi.org/10.1016/S0040-4039(00)88231-3>