@article{PetersPetersRebienetal.2005,
  author    = {Peters, Karl and Peters, E. M. and Rebien, F. and Linker, Torsten},
  title     = {Crystal structure of methyl (1R,2S,3R,4S)-1-phenyl-3,4-epoxi-1,2,3,4-tetrahydronaphthalene-2-carboxy late,C18H16O3},
  issn      = {1433-7266},
  year      = {2005},
  abstract  = {C18H16O3, monoclinic, P12(1)/c1 (no. 14), a = 14.954(3) angstrom, b = 8.088(2) angstrom, c = 11.973(2) angstrom, beta = 93.50(1)degrees, V = 1445.4 angstrom(3), Z = 4, R-gt(F) = 0.083, wR(ref)(F-2) = 0.249, T = 293 K.},
  language  = {en}
}
@article{PetersPetersLinkeretal.2005,
  author    = {Peters, Karl and Peters, E. M. and Linker, Ursula and Linker, Torsten},
  title     = {Crystal structure of 1,1,2,2-tetramethoxycarbonylethanol, C2H(CH3OCO)(4)OH},
  issn      = {1433-7266},
  year      = {2005},
  abstract  = {C10H14O9, monoclinic, C12/c1 (no. 15), a = 15.801(1) angstrom, b = 7.920(1) angstrom, c = 21.055(2) angstrom, beta = 101.31 (1)degrees, V = 2583.8 angstrom(3), Z = 8, R-gt(F) 0.044, wR(ref)(F-2) = 0.134, T = 293 K.},
  language  = {en}
}
@article{PetersPetersKimetal.2005,
  author    = {Peters, Karl and Peters, E. M. and Kim, Boo Geun and Linker, Torsten},
  title     = {Crystal structure of ethyl (3aR,4R,5R,6R,7aR)-4,5-diacetoxy-6-acetoxymethyl-2-oxy-3a,5,6,7a-tetrahy dro-4H- pyrano[3,2-d]isoxazole-3-carboxylate, C16H21NO11},
  issn      = {1433-7266},
  year      = {2005},
  abstract  = {C16H21NO11, monoclinic, P12(1)1 (no. 4), a = 8.181(1) angstrom, b = 11.604(2) angstrom, c = 10.193(1) angstrom, beta = 101.59(1)degrees, V = 947.9 angstrom(3), Z = 2, R-gt(F) = 0.068, wR(ref)(F-2) = 0.177, T = 293 K.},
  language  = {en}
}
@article{KimSchildeLinker2005,
  author    = {Kim, Boo Geun and Schilde, Uwe and Linker, Torsten},
  title     = {New radical approaches to 3-deoxy-D-oct-2-ulosonic acids (KDO)},
  issn      = {0039-7881},
  year      = {2005},
  abstract  = {Two different approaches. with an unsaturated carbohydrate as a radical acceptor and a carbohydrate derived aldehyde as a radical precursor, led to key intermediates in the synthesis of 3-deoxy-D-oct-2-ulosonic acids (KDO). Manganese(III) acetate and cerium(IV) ammonium nitrate were the reagents of choice for the oxidative generation of radicals, whereas samarium(II) iodide was employed for reductive couplings. Both strategies were realized by using easily available starting materials, with acetic acid as C-2 and ethyl acrylate as C-3 building blocks, respectively},
  language  = {en}
}
@article{EngelhardtLinker2005,
  author    = {Engelhardt, Ulrike and Linker, Torsten},
  title     = {1,4-cyclohexadienes as mechanistic probes for the Jacobsen epoxidation : evidence for radical pathways},
  year      = {2005},
  abstract  = {1,4-Cyclohexadienes allow a direct comparison of epoxidation and C - H oxidation within the same molecule and give evidence for radical pathways during the Jacobsen epoxidation},
  language  = {en}
}
@article{FudickarFeryLinker2005,
  author    = {Fudickar, Werner and Fery, Andreas and Linker, Torsten},
  title     = {Reversible light and air-driven lithography by singlet oxygen},
  issn      = {0002-7863},
  year      = {2005},
  language  = {en}
}