Pure and Applied Chemistry

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• Altiti Ahmad S., Mootoo David R.: Intramolecular Nitrogen Delivery for the Synthesis of C-Glycosphingolipids. Application to the C-Glycoside of the Immunostimulant KRN7000. Org. Lett. 2014, 16, 1466. <http://dx.doi.org/10.1021/ol5002686>
• Brindle Cheyenne S., Yeung Charles S., Jacobsen Eric N.: Chiral β-iodoamines by urea-catalysed iodocyclization of trichloroacetimidates. Chem. Sci. 2013, 4, 2100. <http://dx.doi.org/10.1039/c3sc50410g>
• Seebach Dieter, Beck Albert K., Badine D. Michael, Limbach Michael, Eschenmoser Albert, Treasurywala Adi M., Hobi Reinhard, Prikoszovich Walter, Linder Bernard: Are Oxazolidinones Really Unproductive, Parasitic Species in Proline Catalysis? – Thoughts and Experiments Pointing to an Alternative View. HCA 2007, 90, 425. <http://dx.doi.org/10.1002/hlca.200790050>
• Galeazzi Roberta, Martelli Gianluca, Mobbili Giovanna, Orena Mario, Rinaldi Samuele: Stereoselective iodocyclisation of 3-acylamino-2-methylene alkanoates: a computational insight. Tetrahedron 2006, 62, 10450. <http://dx.doi.org/10.1016/j.tet.2006.08.015>
• Ciclosi Marco, Fava Cristiana, Galeazzi Roberta, Orena Mario, González-Rosende Maria Eugenia, Sepúlveda-Arques José: Homochiral oxazolidin-2-ones and imidazolidin-2-ones by tandem nucleophilic addition–conjugate addition. Tet Asymm 2004, 15, 1937. <http://dx.doi.org/10.1016/j.tetasy.2004.05.006>
• Friesen Richard W., Giroux André, Cook Katherine L.: Iodocyclization reactions of α-allenic alcohol derivatives. Stereoselective formation of Z-4-(1-iodo-2-alkyl)ethylene-2-trichloromethyl-4,5-dihydro-1,3-oxazoles. Tetrahetron Lett 1993, 34, 5983. <http://dx.doi.org/10.1016/S0040-4039(00)61707-0>
• Urabe Hirokazu, Aoyama Yoshiaki, Sato Fumie: Ring opening of the epoxide moiety of (2S, 3S, 4S)-4-amino-2,3-epoxy-1-alkanol and its derivatives: A key role of Ti(O-i-Pr)4 as a mild catalyst. Tetrahedron 1992, 48, 5639. <http://dx.doi.org/10.1016/0040-4020(92)80014-7>
• Slassi A, Guindon Y, Ghiro É, Bantle G, Jung G: Stereoselective silver triflate-mediated iodocyclization of carbamates. Tetrahetron Lett 1992, 33, 4257. <http://dx.doi.org/10.1016/S0040-4039(00)74232-8>
• Cardillo Giuliana, Orena Mario: Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates. Tetrahedron 1990, 46, 3321. <http://dx.doi.org/10.1016/S0040-4020(01)81510-6>
• Michael Joseph P., Nkwelo Mluleki M.: Heterocyclisations induced by thallium(III) acetate. Effect of varying the internal nucleophile. Tetrahedron 1990, 46, 2549. <http://dx.doi.org/10.1016/S0040-4020(01)82035-4>
• Fox David N.A., Gallagher Timothy: Asymmetric synthesis via electrophile-mediated cyclisations. Tetrahedron 1990, 46, 4697. <http://dx.doi.org/10.1016/S0040-4020(01)85590-3>
• Friesen Richard W: A highly stereoselective conversion of α-allenic alcohols to 1,2-syn amino alcohol derivatives via iodocarbamation. Tetrahetron Lett 1990, 31, 4249. <http://dx.doi.org/10.1016/S0040-4039(00)97592-0>
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