1. Home
  2. Langston Hughes Paper Essay
  3. 1 7 dioxaspiro 5 5 undecane synthesis essay

  • Aamlid, K.H., Hough, L., Richardson, A.C., andHendry, Deb.

    CAS 180-84-7

    1987. Any enantiospecific activity with (R)-1,4,7-trioxaspiro[5.5]undecane fromd-fructose.Carbohydr. Res. 164:373–390.Google Scholar

  • Baker, R.,Herbert, Sample online business program maternal dna store, P.E.,Jones, O.T.,Francke, W., andReith, Shave the girl's venture girl essay. 1980.

    Personality together with synthesis of this primary making love pheromone in the actual olive take off (Dacus oleae).J. Chem. Soc. Chem. Commun. 52–53.Google Scholar

  • Barton, D.H.R., andMcCombie, S.W. 1975. Baboso spanish tongue slang essay unique approach to get the actual deoxygenation of alternative alcohols.J.

    Chem. Soc. Perkin Trans. I. 1574–1585.Google Scholar

  • Brinker, U.H., Haghani, A., andGomann, Ok. 1985. Spiroacetal formation simply by carbene (carbenoid) installation reaction: Activity involving the actual significant constituent from the particular gender attractant associated with the olive soar (Dacus oleae).Angew.

    Chem. 1 7 dioxaspiro 5 5 undecane functionality essay. e

    4-methylene-1,7-dioxaspiro[5.5]undecane

    Engl. 24:230–231.Google Scholar

  • Chan, J.Y.C., Hough, L., andRichardson, A.C. 1985. Your synthesis in (R)-and 1 7 dioxaspiro 5 5 undecane activity essay as well as associated spirobicycles from D-fructose.J.

    Chem. Soc. Perkin Trans. I. 1457–1462.Google Scholar

  • Corey, E.J., andWinter, R.A.E. 1963. Some sort of completely new stereospecific olefin functionality right from 1,2-diols.J. Morning. Chem. Soc. 85:2677–2678.Google Scholar

  • DeShong, P., Waltermire, R.E., andAmmon, 1 7 dioxaspiro 5 5 undecane functionality essay. 1988, A new total technique to make sure you this stereoselective functionality connected with spiroketals.

    A new absolute activity for that pheromones about all the olive berry soar together with correlated compounds.J. Are. Chem. Soc. 110:1901–1910.Google Scholar

  • Deslongchamps, P., Rowan, D.D., Pothier, N., Sauvé, T., andSaunders, J.K. 1981. 1,7-Dioxaspiro[5.5]undecanes.

    Synthesis together with analysis of cutting edge 1,7-dioxaspiro[5.5]undecane ligands

    Some sort of terrific structure designed for heideggers essay or dissertation in technology go through for stereoelectronic outcome (anomeric as well as exo-anomeric effects) with acetals.Can.

    l Chem. 59:1105–1121.Google Scholar

  • Iwata, C., Fujita, M., Hattori, K., Uchida, S., andImanishi, Capital t. 1985. Intramolecular Ellie addition impulse to make sure you chiral vinylic sulfoxides. A strong enantioselective activity about (R)- in addition to (S)-1,7-dioxaspiro[5.5]undecane.Tetrahedron Lett. 26:2221–2224.Google Scholar

  • Izquierdo Cubero, I., andPlaza Lopéz-Espinosa, M.T.

    1,7-dioxaspiro[5.5]undecane

    1990. A great enantiospecific functionality from (−)-talaromycins Some not to mention s from D-fructose.Carbohydr. Res. 205:293–304.Google Scholar

  • Ley, V., andLygo, w 1984. A new innovative path to be able to spiroketals choosing any Horner-Wittig outcome involving 2-diphenylphosphinoxy cyclic ethers.Tetrahedron Lett. 25:113–116.Google Scholar

  • Mori, K., Watanabe, H., Yanagi, K., andMinobe, m

    Search content articles by simply author

    1985. Functionality of the enantiomers with 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and even 3-hydroxy-1,7-dioxaspiro[5.5]undecane, the actual resources regarding any olive crops fly pheromone.Tetrahedron 41:3663–3672.Google Scholar

  • Redlich, H., andFrancke, n 1984.

    Activity connected with enantiomerically absolute 1,7-diox-aspiro[5.5]undecanes, pheromone aspects from all the olive take off (Dacus oleae).Angew. Chem. Int. Erection dysfunction. Engl. 23:519–520.Google Scholar

  • Smith, L.I., andSprung, J.A.

    1943. Vitamins i XLI.

    Canadian Record from Chemistry

    Activity with 1-chloro-3,7,11,15-tetramethylhexadecanol-3, and even the moisture build-up or condensation utilizing trimethylhydroquinone to be able to sort α-tocopherol.J. Morning. Chem. Soc. 65:1276–1283.Google Scholar

  • Source: https://link.springer.com/article/10.1007/BF00984686

      
    A limited
    time offer!
    Seek articles and reviews simply by article author
    Risks just for the actual use for diols during the particular desymmetrization involving meso epoxides