##############################################################################
###                                                                        ###
###        Electronic paper (Acta Crystallographica Section E)             ###
###                                                                        ###
##############################################################################
#                                                                            #
# This CIF contains the data in a paper accepted for publication in Acta     #
# Crystallographica Section E. It conforms to the requirements of Notes      #
# for Authors for Section E, and has been peer reviewed under the auspices   #
# of the IUCr Commission on Journals.                                        #
#                                                                            #
# Full details of the Crystallographic Information File format               #
# are given in the paper "The Crystallographic Information File (CIF):       #
# a New Standard Archive File for Crystallography" by S. R. Hall, F. H.      #
# Allen and I. D. Brown [Acta Cryst. (1991), A47, 655-685].                  #
#                                                                            #
# The current version of the core CIF dictionary is obtainable from          #
# ftp://ftp.iucr.org/pub/cif_core.dic. The current version number is 2.1.    #
#                                                                            #
# Software is freely available for graphical display of the structure(s) in  #
# this CIF.  For information consult the CIF home page http://www.iucr.org/  #
# cif/home.html                                                              #
#                                                                            #
#            Copyright International Union of Crystallography                #
#                                                                            #
##############################################################################
                                             
data_I
_audit_creation_method     SHELXL-97
_chemical_name_systematic
;
Methyl 2,3,4-tri-O-pivaloyl-β-D-xylopyranoside
;
_chemical_name_common     ?
_chemical_formula_moiety     'C21 H36 O8'
_chemical_formula_sum     'C21 H36 O8'
_chemical_formula_iupac     'C21 H36 O8'
_chemical_formula_weight     416.50
_chemical_melting_point     ?
_symmetry_cell_setting     monoclinic
_symmetry_space_group_name_H-M     'P 21'
_symmetry_space_group_name_Hall     'P 2yb'
loop_
    _symmetry_equiv_pos_as_xyz
    'x, y, z'
    '-x, y+1/2, -z'
_cell_length_a     9.8280(10)
_cell_length_b     6.8490(10)
_cell_length_c     17.6340(10)
_cell_angle_alpha     90.000
_cell_angle_beta     96.360(10)
_cell_angle_gamma     90.000
_cell_volume     1179.7(2)
_cell_formula_units_Z     2
_cell_measurement_reflns_used     1573
_cell_measurement_theta_min     15.00
_cell_measurement_theta_max     25.00
_cell_measurement_temperature     100(2)
_exptl_crystal_description     prismatic
_exptl_crystal_colour     colorless
_exptl_crystal_size_max     0.3
_exptl_crystal_size_mid     0.3
_exptl_crystal_size_min     0.2
_exptl_crystal_density_diffrn     1.173
_exptl_crystal_density_meas     ?
_exptl_crystal_density_method     'not measured'
_exptl_crystal_F_000     452
_exptl_absorpt_coefficient_mu     0.089
_exptl_absorpt_correction_type     none
_exptl_absorpt_process_details     ?
_exptl_absorpt_correction_T_min     ?
_exptl_absorpt_correction_T_max     ?
_exptl_special_details
;
The data did not permit the determination of the absolute structure;
(the stereochemistry is the relative configuration based on the
absolute stereochemistry of related compounds).
;
_diffrn_ambient_temperature     100(2)
_diffrn_radiation_type     MoK\a
_diffrn_radiation_wavelength     0.71069
_diffrn_radiation_source     'fine-focus sealed tube'
_diffrn_radiation_monochromator     'graphite'
_diffrn_measurement_device_type     'Xcalibur CCD'
_diffrn_measurement_method     'ω'
_diffrn_detector_area_resol_mean     ?
_diffrn_reflns_number     38147
_diffrn_reflns_av_R_equivalents     0.0883
_diffrn_reflns_av_sigmaI/netI     0.0299
_diffrn_reflns_theta_min     4.55
_diffrn_reflns_theta_max     29.00
_diffrn_reflns_theta_full     29.00
_diffrn_measured_fraction_theta_max     0.994
_diffrn_measured_fraction_theta_full     0.994
_diffrn_reflns_limit_h_min     -13
_diffrn_reflns_limit_h_max     13
_diffrn_reflns_limit_k_min     -9
_diffrn_reflns_limit_k_max     9
_diffrn_reflns_limit_l_min     -24
_diffrn_reflns_limit_l_max     24
_diffrn_standards_number     '3 reference frames'
_diffrn_standards_interval_count     '50 frames'
_diffrn_standards_interval_time     ?
_diffrn_standards_decay_%     none
_refine_special_details
;
  Refinement of F² against ALL reflections.  The weighted R-factor wR and
  goodness of fit S are based on F², conventional R-factors R are based
  on F, with F set to zero for negative F². The threshold expression of
  F² > 2sigma(F²) is used only for calculating R-factors(gt) etc. and is
  not relevant to the choice of reflections for refinement.  R-factors based
  on F² are statistically about twice as large as those based on F, and R-
  factors based on ALL data will be even larger.
;
_reflns_number_total     3376
_reflns_number_gt     3234
_reflns_threshold_expression     I>2σ(I)
_refine_ls_structure_factor_coef     Fsqd
_refine_ls_matrix_type     full
_refine_ls_R_factor_all     0.0406
_refine_ls_R_factor_gt     0.0390
_refine_ls_wR_factor_gt     0.0933
_refine_ls_wR_factor_ref     0.0944
_refine_ls_goodness_of_fit_ref     1.143
_refine_ls_restrained_S_all     1.143
_refine_ls_number_reflns     3376
_refine_ls_number_parameters     406
_refine_ls_number_restraints     1
_refine_ls_hydrogen_treatment     mixed
_refine_ls_weighting_scheme     calc
_refine_ls_weighting_details
     'calc w = 1/[σ²(Fo²)+(0.0504P)²+0.2141P] where P = (Fo²+2Fc²)/3'
_atom_sites_solution_hydrogens     difmap
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary     difmap
_refine_ls_shift/su_max     0.000
_refine_ls_shift/su_mean     0.000
_refine_diff_density_max     0.374
_refine_diff_density_min     -0.211
_refine_ls_extinction_method     none
_refine_ls_extinction_coef     ?
_refine_ls_abs_structure_details     ?
_refine_ls_abs_structure_Flack     ?
loop_
    _atom_type_symbol
    _atom_type_description
    _atom_type_scat_dispersion_real
    _atom_type_scat_dispersion_imag
    _atom_type_scat_source
    'C' 'C' 0.0033 0.0016
                         'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
    'H' 'H' 0.0000 0.0000
                         'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
    'O' 'O' 0.0106 0.0060
                         'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
_computing_data_collection     'CrysAlis CCD (Oxford Diffraction, 2003)'
_computing_cell_refinement     'CrysAlis RED (Oxford Diffraction, 2003)'
_computing_data_reduction     'CrysAlis RED'
_computing_structure_solution     'SIR97 (Altomare et al., 1999)'
_computing_structure_refinement     'SHELXL97 (Sheldrick, 1997)'
_computing_molecular_graphics     'PLATON98 (Spek, 2003)'
_computing_publication_material     'SHELXL97'
loop_
    _atom_site_label
    _atom_site_fract_x
    _atom_site_fract_y
    _atom_site_fract_z
    _atom_site_U_iso_or_equiv
    _atom_site_adp_type
    _atom_site_calc_flag
    _atom_site_refinement_flags
    _atom_site_occupancy
    _atom_site_disorder_assembly
    _atom_site_disorder_group
    _atom_site_type_symbol
    O1 0.90467(12) 0.9963(2) 0.27885(7) 0.0210(3) Uani d . 1 . . O
    O2 0.67472(12) 1.14493(19) 0.33822(6) 0.0177(2) Uani d . 1 . . O
    O3 0.43427(12) 1.17869(19) 0.23208(7) 0.0181(2) Uani d . 1 . . O
    O4 0.40081(11) 0.8702(2) 0.12167(6) 0.0206(3) Uani d . 1 . . O
    O5 0.77279(11) 0.8747(2) 0.17460(7) 0.0206(3) Uani d . 1 . . O
    O6 0.73886(19) 1.4510(2) 0.31265(8) 0.0374(4) Uani d . 1 . . O
    O7 0.33988(13) 1.0393(2) 0.33006(7) 0.0236(3) Uani d . 1 . . O
    O8 0.41444(17) 1.0010(3) 0.00617(9) 0.0502(5) Uani d . 1 . . O
    C1 0.77493(15) 0.9275(3) 0.25305(9) 0.0168(3) Uani d . 1 . . C
    C2 0.67251(16) 1.0922(3) 0.25932(9) 0.0143(3) Uani d . 1 . . C
    C3 0.52954(15) 1.0189(3) 0.23020(9) 0.0150(3) Uani d . 1 . . C
    C4 0.53234(16) 0.9531(3) 0.14832(9) 0.0171(3) Uani d . 1 . . C
    C5 0.64225(17) 0.7965(3) 0.14567(10) 0.0213(3) Uani d . 1 . . C
    C6 1.00126(17) 0.8407(3) 0.29381(12) 0.0262(4) Uani d . 1 . . C
    C7 0.71448(17) 1.3291(3) 0.35805(9) 0.0207(3) Uani d . 1 . . C
    C8 0.72651(18) 1.3565(3) 0.44436(10) 0.0258(4) Uani d . 1 . . C
    C9 0.8546(3) 1.2435(6) 0.47813(14) 0.0492(7) Uani d . 1 . . C
    C10 0.7413(4) 1.5740(5) 0.46246(15) 0.0500(7) Uani d . 1 . . C
    C11 0.5994(2) 1.2767(4) 0.47661(12) 0.0373(5) Uani d . 1 . . C
    C12 0.34523(16) 1.1722(3) 0.28597(9) 0.0163(3) Uani d . 1 . . C
    C13 0.25306(16) 1.3526(3) 0.28059(9) 0.0181(3) Uani d . 1 . . C
    C14 0.3382(2) 1.5371(3) 0.27308(12) 0.0254(4) Uani d . 1 . . C
    C15 0.1789(2) 1.3636(3) 0.35238(10) 0.0261(4) Uani d . 1 . . C
    C16 0.14786(17) 1.3264(3) 0.20974(10) 0.0226(4) Uani d . 1 . . C
    C17 0.35381(17) 0.9045(3) 0.04765(10) 0.0231(4) Uani d . 1 . . C
    C18 0.21880(18) 0.7985(3) 0.02499(10) 0.0234(4) Uani d . 1 . . C
    C19 0.11581(19) 0.8528(4) 0.08105(13) 0.0345(5) Uani d . 1 . . C
    C20 0.1646(2) 0.8584(4) -0.05658(12) 0.0358(5) Uani d . 1 . . C
    C21 0.2473(2) 0.5787(3) 0.02853(12) 0.0297(4) Uani d . 1 . . C
    H1 0.748(2) 0.813(3) 0.2817(12) 0.012(5) Uiso d . 1 . . H
    H2 0.696(2) 1.203(3) 0.2313(12) 0.012(5) Uiso d . 1 . . H
    H3 0.504(2) 0.910(3) 0.2612(11) 0.011(5) Uiso d . 1 . . H
    H4 0.554(2) 1.060(4) 0.1196(12) 0.015(5) Uiso d . 1 . . H
    H51 0.618(2) 0.680(4) 0.1751(14) 0.024(6) Uiso d . 1 . . H
    H52 0.650(2) 0.759(4) 0.0963(13) 0.020(5) Uiso d . 1 . . H
    H61 1.089(3) 0.904(4) 0.3153(15) 0.033(7) Uiso d . 1 . . H
    H62 0.970(3) 0.749(4) 0.3303(16) 0.036(7) Uiso d . 1 . . H
    H63 1.015(3) 0.765(4) 0.2466(15) 0.031(6) Uiso d . 1 . . H
    H91 0.846(4) 1.107(6) 0.466(2) 0.057(10) Uiso d . 1 . . H
    H92 0.863(3) 1.261(6) 0.533(2) 0.066(10) Uiso d . 1 . . H
    H93 0.940(4) 1.297(6) 0.459(2) 0.066(10) Uiso d . 1 . . H
    H101 0.818(4) 1.629(6) 0.446(2) 0.066(11) Uiso d . 1 . . H
    H102 0.652(4) 1.646(7) 0.439(2) 0.086(14) Uiso d . 1 . . H
    H103 0.748(4) 1.585(7) 0.522(2) 0.073(11) Uiso d . 1 . . H
    H111 0.590(3) 1.130(5) 0.4669(17) 0.044(8) Uiso d . 1 . . H
    H112 0.610(3) 1.298(5) 0.5322(17) 0.041(7) Uiso d . 1 . . H
    H113 0.515(3) 1.348(6) 0.4560(17) 0.051(8) Uiso d . 1 . . H
    H141 0.280(2) 1.655(4) 0.2735(13) 0.022(5) Uiso d . 1 . . H
    H142 0.413(3) 1.550(5) 0.3189(16) 0.038(7) Uiso d . 1 . . H
    H143 0.383(3) 1.538(5) 0.2262(16) 0.039(7) Uiso d . 1 . . H
    H151 0.113(3) 1.479(5) 0.3487(17) 0.040(7) Uiso d . 1 . . H
    H152 0.125(3) 1.246(5) 0.3617(18) 0.042(8) Uiso d . 1 . . H
    H153 0.244(3) 1.385(5) 0.3980(16) 0.043(8) Uiso d . 1 . . H
    H161 0.091(2) 1.210(4) 0.2149(13) 0.017(5) Uiso d . 1 . . H
    H162 0.191(2) 1.310(4) 0.1663(14) 0.025(6) Uiso d . 1 . . H
    H163 0.085(3) 1.445(4) 0.2023(15) 0.033(7) Uiso d . 1 . . H
    H191 0.153(3) 0.821(5) 0.1338(17) 0.039(7) Uiso d . 1 . . H
    H192 0.029(3) 0.781(5) 0.0696(16) 0.035(7) Uiso d . 1 . . H
    H193 0.096(3) 0.989(6) 0.0821(19) 0.052(9) Uiso d . 1 . . H
    H201 0.145(3) 0.992(5) -0.0610(16) 0.037(7) Uiso d . 1 . . H
    H202 0.078(3) 0.792(5) -0.0687(16) 0.040(7) Uiso d . 1 . . H
    H203 0.229(3) 0.820(5) -0.0927(18) 0.052(9) Uiso d . 1 . . H
    H211 0.279(3) 0.542(5) 0.0833(17) 0.044(8) Uiso d . 1 . . H
    H212 0.161(3) 0.509(6) 0.0114(18) 0.056(9) Uiso d . 1 . . H
    H213 0.313(3) 0.542(5) -0.0068(18) 0.050(8) Uiso d . 1 . . H
_geom_special_details
;
  All esds (except the esd in the dihedral angle between two l.s. planes)
  are estimated using the full covariance matrix.  The cell esds are taken
  into account individually in the estimation of esds in distances, angles
  and torsion angles; correlations between esds in cell parameters are only
  used when they are defined by crystal symmetry.  An approximate (isotropic)
  treatment of cell esds is used for estimating esds involving l.s. planes.
;
loop_
    _geom_bond_atom_site_label_1
    _geom_bond_atom_site_label_2
    _geom_bond_site_symmetry_2
    _geom_bond_distance
    _geom_bond_publ_flag
    O1 C1 . 1.3881(19) y
    O1 C6 . 1.432(2) n
    O2 C7 . 1.355(2) n
    O2 C2 . 1.4352(18) y
    O3 C12 . 1.3620(19) n
    O3 C3 . 1.443(2) y
    O4 C17 . 1.3560(19) n
    O4 C4 . 1.4421(19) y
    O5 C1 . 1.4278(19) y
    O5 C5 . 1.431(2) y
    O6 C7 . 1.199(2) n
    O7 C12 . 1.202(2) n
    O8 C17 . 1.193(2) n
    C1 C2 . 1.524(2) y
    C1 H1 . 0.99(2) n
    C2 C3 . 1.527(2) y
    C2 H2 . 0.95(2) n
    C3 C4 . 1.515(2) y
    C3 H3 . 0.98(2) n
    C4 C5 . 1.527(2) y
    C4 H4 . 0.93(2) n
    C5 H51 . 1.00(3) n
    C5 H52 . 0.92(2) n
    C6 H61 . 1.00(3) n
    C6 H62 . 0.97(3) n
    C6 H63 . 1.00(3) n
    C7 C8 . 1.525(2) n
    C8 C10 . 1.527(4) n
    C8 C11 . 1.530(3) n
    C8 C9 . 1.540(3) n
    C9 H91 . 0.96(4) n
    C9 H92 . 0.97(4) n
    C9 H93 . 1.01(4) n
    C10 H101 . 0.92(4) n
    C10 H102 . 1.05(5) n
    C10 H103 . 1.05(4) n
    C11 H111 . 1.02(3) n
    C11 H112 . 0.99(3) n
    C11 H113 . 1.00(3) n
    C12 C13 . 1.529(2) n
    C13 C14 . 1.530(3) n
    C13 C15 . 1.531(2) n
    C13 C16 . 1.541(2) n
    C14 H141 . 0.99(3) n
    C14 H142 . 1.03(3) n
    C14 H143 . 0.98(3) n
    C15 H151 . 1.02(3) n
    C15 H152 . 0.99(3) n
    C15 H153 . 0.98(3) n
    C16 H161 . 0.98(2) n
    C16 H162 . 0.92(2) n
    C16 H163 . 1.02(3) n
    C17 C18 . 1.526(2) n
    C18 C21 . 1.532(3) n
    C18 C20 . 1.533(3) n
    C18 C19 . 1.537(3) n
    C19 H191 . 0.99(3) n
    C19 H192 . 0.98(3) n
    C19 H193 . 0.96(4) n
    C20 H201 . 0.93(3) n
    C20 H202 . 0.97(3) n
    C20 H203 . 0.98(3) n
    C21 H211 . 1.01(3) n
    C21 H212 . 0.99(3) n
    C21 H213 . 0.98(3) n
loop_
    _geom_angle_atom_site_label_1
    _geom_angle_atom_site_label_2
    _geom_angle_atom_site_label_3
    _geom_angle_site_symmetry_1
    _geom_angle_site_symmetry_3
    _geom_angle
    _geom_angle_publ_flag
    C1 O1 C6 . . 111.93(14) n
    C7 O2 C2 . . 117.23(13) n
    C12 O3 C3 . . 117.38(13) n
    C17 O4 C4 . . 116.30(13) n
    C1 O5 C5 . . 110.88(12) y
    O1 C1 O5 . . 108.55(12) y
    O1 C1 C2 . . 108.35(14) y
    O5 C1 C2 . . 108.59(12) y
    O1 C1 H1 . . 113.0(12) n
    O5 C1 H1 . . 108.6(12) n
    C2 C1 H1 . . 109.6(12) n
    O2 C2 C1 . . 108.51(12) y
    O2 C2 C3 . . 108.88(12) y
    C1 C2 C3 . . 108.82(13) y
    O2 C2 H2 . . 108.9(13) n
    C1 C2 H2 . . 110.9(12) n
    C3 C2 H2 . . 110.9(12) n
    O3 C3 C4 . . 109.13(13) y
    O3 C3 C2 . . 108.55(14) y
    C4 C3 C2 . . 107.77(12) y
    O3 C3 H3 . . 111.0(12) n
    C4 C3 H3 . . 109.9(12) n
    C2 C3 H3 . . 110.5(12) n
    O4 C4 C3 . . 108.50(12) y
    O4 C4 C5 . . 108.97(15) y
    C3 C4 C5 . . 109.00(13) y
    O4 C4 H4 . . 112.6(13) n
    C3 C4 H4 . . 108.4(14) n
    C5 C4 H4 . . 109.2(13) n
    O5 C5 C4 . . 109.61(14) y
    O5 C5 H51 . . 112.0(14) n
    C4 C5 H51 . . 109.4(14) n
    O5 C5 H52 . . 105.9(14) n
    C4 C5 H52 . . 111.2(15) n
    H51 C5 H52 . . 109(2) n
    O1 C6 H61 . . 105.9(17) n
    O1 C6 H62 . . 110.7(16) n
    H61 C6 H62 . . 110(2) n
    O1 C6 H63 . . 112.3(16) n
    H61 C6 H63 . . 111(2) n
    H62 C6 H63 . . 107(2) n
    O6 C7 O2 . . 123.31(16) n
    O6 C7 C8 . . 125.55(18) n
    O2 C7 C8 . . 111.13(15) n
    C7 C8 C10 . . 108.88(18) n
    C7 C8 C11 . . 110.53(15) n
    C10 C8 C11 . . 109.5(2) n
    C7 C8 C9 . . 107.08(17) n
    C10 C8 C9 . . 110.8(2) n
    C11 C8 C9 . . 110.1(2) n
    C8 C9 H91 . . 110(2) n
    C8 C9 H92 . . 108(2) n
    H91 C9 H92 . . 110(3) n
    C8 C9 H93 . . 111(2) n
    H91 C9 H93 . . 110(3) n
    H92 C9 H93 . . 108(3) n
    C8 C10 H101 . . 113(3) n
    C8 C10 H102 . . 109(3) n
    H101 C10 H102 . . 111(4) n
    C8 C10 H103 . . 106(2) n
    H101 C10 H103 . . 109(3) n
    H102 C10 H103 . . 108(3) n
    C8 C11 H111 . . 110.7(17) n
    C8 C11 H112 . . 108.6(17) n
    H111 C11 H112 . . 108(2) n
    C8 C11 H113 . . 112.0(19) n
    H111 C11 H113 . . 111(3) n
    H112 C11 H113 . . 106(2) n
    O7 C12 O3 . . 123.62(16) n
    O7 C12 C13 . . 125.74(14) n
    O3 C12 C13 . . 110.63(14) n
    C12 C13 C14 . . 110.32(13) n
    C12 C13 C15 . . 108.77(14) n
    C14 C13 C15 . . 110.23(16) n
    C12 C13 C16 . . 107.22(14) n
    C14 C13 C16 . . 110.49(15) n
    C15 C13 C16 . . 109.75(14) n
    C13 C14 H141 . . 110.7(14) n
    C13 C14 H142 . . 110.7(17) n
    H141 C14 H142 . . 106(2) n
    C13 C14 H143 . . 112.3(18) n
    H141 C14 H143 . . 108(2) n
    H142 C14 H143 . . 108(2) n
    C13 C15 H151 . . 110.1(17) n
    C13 C15 H152 . . 114.1(18) n
    H151 C15 H152 . . 107(2) n
    C13 C15 H153 . . 111.1(16) n
    H151 C15 H153 . . 107(3) n
    H152 C15 H153 . . 107(3) n
    C13 C16 H161 . . 110.8(13) n
    C13 C16 H162 . . 111.0(15) n
    H161 C16 H162 . . 107(2) n
    C13 C16 H163 . . 110.8(16) n
    H161 C16 H163 . . 108.4(19) n
    H162 C16 H163 . . 108(2) n
    O8 C17 O4 . . 123.09(16) n
    O8 C17 C18 . . 125.57(16) n
    O4 C17 C18 . . 111.31(14) n
    C17 C18 C21 . . 107.88(16) n
    C17 C18 C20 . . 108.69(16) n
    C21 C18 C20 . . 110.12(18) n
    C17 C18 C19 . . 109.41(15) n
    C21 C18 C19 . . 109.99(19) n
    C20 C18 C19 . . 110.71(18) n
    C18 C19 H191 . . 110.5(16) n
    C18 C19 H192 . . 111.4(16) n
    H191 C19 H192 . . 108(2) n
    C18 C19 H193 . . 114(2) n
    H191 C19 H193 . . 105(3) n
    H192 C19 H193 . . 109(3) n
    C18 C20 H201 . . 112.7(18) n
    C18 C20 H202 . . 106.7(17) n
    H201 C20 H202 . . 106(3) n
    C18 C20 H203 . . 110.7(18) n
    H201 C20 H203 . . 110(3) n
    H202 C20 H203 . . 110(2) n
    C18 C21 H211 . . 108.7(18) n
    C18 C21 H212 . . 108(2) n
    H211 C21 H212 . . 110(3) n
    C18 C21 H213 . . 111(2) n
    H211 C21 H213 . . 113(3) n
    H212 C21 H213 . . 107(3) n
data_global
_journal_date_recd_electronic     2004-09-09
_journal_date_accepted     2004-09-14
_journal_name_full     'Acta Crystallographica, Section E'
_journal_year     2004
_journal_volume     60
_journal_issue     10
_journal_page_first     o1840
_journal_page_last     o1841
_journal_paper_category     EO
_publ_contact_author
;
        Dubravka Matković-Čalogović
        Laboratory of General and Inorganic Chemistry
        Department of Chemistry
        Faculty of Science
        University of Zagreb
        Kralja Zvonimira 8
        HR-10000 Zagreb, Croatia
;
_publ_contact_author_email     dubravka@chem.pmf.hr
_publ_contact_author_fax     '+385 1 4611191'
_publ_contact_author_phone     '+385 1 4606692'
_publ_section_title
;
Methyl 2,3,4-tri-O-pivaloyl-β-D-xylopyranoside
;
loop_
    _publ_author_name
    _publ_author_address
    'Prugovečki, Biserka'
;
Laboratory of General and Inorganic Chemistry
Department of Chemistry
Faculty of Science
University of Zagreb
Kralja Zvonimira 8
HR-10000 Zagreb
Croatia
;
    'Matković-Čalogović, Dubravka'
;
Laboratory of General and Inorganic Chemistry
Department of Chemistry
Faculty of Science
University of Zagreb
Kralja Zvonimira 8
HR-10000 Zagreb
Croatia
;
    'Petrović, Vesna'
;
Laboratory of Organic Chemistry
Department of Chemistry
Faculty of Science
University of Zagreb
Strossmayerov trg 14
HR-10000 Zagreb
Croatia
;
    'Tomić, Srđanka'
;
Laboratory of Organic Chemistry
Department of Chemistry
Faculty of Science
University of Zagreb
Strossmayerov trg 14
HR-10000 Zagreb
Croatia
;
