CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1977, Vol. 49, No. 8, pp. 1201-1214

http://dx.doi.org/10.1351/pac197749081201

Approaches to the total synthesis of natural products from carbohydrates

S. Hanessian and G. Rancourt

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Yin Jian, Linker Torsten: Recent advances in the stereoselective synthesis of carbohydrate 2-C-analogs. Biomol Chem 2012, 10, 2351. <http://dx.doi.org/10.1039/c2ob06529k>
  • Rele Shyam, Nayak Sandip K.: LOW-VALENT TITANIUM MEDIATED REDUCTIVE CLEAVAGE OF O/N-TRITYL BONDS VIA FREE RADICAL PATHWAY. Synth Common 2002, 32, 3533. <http://dx.doi.org/10.1081/SCC-120014795>
  • Evans David A., Trotter B.Wesley, Coleman Paul J., Côté Bernard, Dias Luiz Carlos, Rajapakse Hemaka A., Tyler Andrew N.: Enantioselective total synthesis of altohyrtin C (spongistatin 2). Tetrahedron 1999, 55, 8671. <http://dx.doi.org/10.1016/S0040-4020(99)00438-X>
  • Dorta Rosa L, Francisco Cosme G, Suárez Ernesto: Organoselenium reagents in the tandem β-fragmentation-cyclization of carbohydrate anomeric alkoxy radicals. Tetrahetron Lett 1994, 35, 2049. <http://dx.doi.org/10.1016/S0040-4039(00)73046-2>
  • Krainer Eduardo, Naider Fred, Becker Jeffrey: A new method for the detritylation of alcohols bearing other reducible and acid-hydrolyzable functionalities. Tetrahetron Lett 1993, 34, 1713. <http://dx.doi.org/10.1016/S0040-4039(00)60759-1>
  • de Armas Pedro, Francisco Cosme G., Suárez Ernesto: Reagentien mit hypervalentem Iod: Herstellung chiraler Synthesebausteine durch Fragmentierung anomerer Kohlenhydrat-Alkoxyradikale. Angew Chem 1992, 104, 746. <http://dx.doi.org/10.1002/ange.19921040610>
  • Lankin David C., Nugent Sean T., Rao Shashidhar N.: NMR spectroscopy and conformational analysis of substituted 1,2:5,6-di-O-isopropylidene-α-d-allofuranose derivatives. Carbohydrates Research 1992, 229, 245. <http://dx.doi.org/10.1016/S0008-6215(00)90574-3>
  • Yu Kuo Long, Handa Sheetal, Tsang Raymond, Fraser-Reid Bert: Carbohydrate-derived partners display remarkably high stereoselectivity in aldol coupling reactions. Tetrahedron 1991, 47, 189. <http://dx.doi.org/10.1016/S0040-4020(01)80916-9>
  • Yoshimura Juji, Kawauchi Nobuya, Yasumori Toshio, Sato Ken-ichi, Hashimoto Hironobu: Synthesis of 2,3-anhydro- and 3,4-anhydro-hexopyranosides having a methyl branch on the oxirane ring, and their reactions with some lithium methylcuprate reagents. Carbohydrates Research 1984, 133, 255. <http://dx.doi.org/10.1016/0008-6215(84)85203-9>
  • Hanessian Stephen, Pougny Jean-René, Boessenkool Ideletta K.: Assembly of the c19-c29 aliphatic segment of rifamycin s from d-glucose by the chiron approach. Tetrahedron 1984, 40, 1289. <http://dx.doi.org/10.1016/S0040-4020(01)82415-7>
  • Bargiotti Alberto, Cassinelli Giuseppe, Penco Sergio, Vigevani Aristide, Arcamone Federico: Synthesis of new branched-chain aminodeoxyhexoses related to daunosamine (3-amino-2,3,6-trideoxy-l-lyxo-hexose). Carbohydrates Research 1982, 100, 273. <http://dx.doi.org/10.1016/S0008-6215(00)81041-1>
  • Nakahara Yoshiaki, Beppu Kazuo, Ogawa Tomoya: Synthetic studies on antibiotic A23187 I. Chiral synthons for C9-C13 and C14-C20. Tetrahetron Lett 1981, 22, 3197. <http://dx.doi.org/10.1016/S0040-4039(01)81862-1>
  • Kochetkov N.K., Sviridov A.F., Ermolenko M.S., Zelinsky N.D.: Synthesis of macrolide antibiotics. 1. Synthesis of the C1-C6 segment of 14-membered macrolide antibiotics. Tetrahetron Lett 1981, 22, 4315. <http://dx.doi.org/10.1016/S0040-4039(01)82944-0>
  • Bartlett Paul A.: Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis. Tetrahedron 1980, 36, 2. <http://dx.doi.org/10.1016/0040-4020(80)85026-5>