# Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry
# This journal is © The Royal Society of Chemistry 2012


data_global
_journal_name_full               Org.Biomol.Chem.
_journal_coden_cambridge         0177
#TrackingRef '6289_web_deposit_cif_file_0_BernardOmondi_1310641264.archive.cif'

#------------------ AUDIT DETAILS -------------------------------------------#

_audit_creation_date             2010-10-05
_audit_creation_method           'WinGX routine CIF_UPDATE'
_audit_conform_dict_name         cif_core.dic
_audit_conform_dict_version      2.4
_audit_conform_dict_location     ftp://ftp.iucr.org/pub/cif_core.dic
_audit_update_record             ?

#------------------ AUTHOR DETAILS -------------------------------------------#

# Name and address of author for correspondence

_publ_contact_author_name        'Omondi, Bernard'
_publ_contact_author_address     
;
Research Centre for Synthesis and Catalysis
Department of Chemistry
University of Johannesburg
PO Box 524
Auckland Park, 2006
South Africa

;
_publ_contact_author_email       owaga@ukzn.ac.za
_publ_contact_author_fax         +27(031)2607323
_publ_contact_author_phone       +27(031)2603091

# Insert blank lines between references

_publ_section_references         
;
Bruker (2007) APEX2 (Version 2.1-4), SAINT (version 7.34A), SADABS
(version 2007/4), BrukerAXS Inc, Madison, Wisconsin, USA.

Flack H. D. & Bernardinelli, G. (1999). Acta Cryst. A55, 908-915.

Flack H. D. & Bernardinelli, G. (2000). J. Appl. Cryst. 33, 1143-1148.

APEX, APEX2, SMART, SAINT, SAINT-Plus: Bruker (2007). Program name(s).
Bruker AXS Inc., Madison, Wisconsin, USA.
[Older versions (pre-1997) should refer to Siemens Analytical X-ray
Instruments Inc. instead of Bruker AXS.]

Cambridge Structural Database: Allen, F. R. (2002). Acta Cryst. B58, 380-388.

enCIFer: Allen, F. H., Johnson, O., Shields, G. P., Smith, B. R. & Towler,
M. (2004). J. Appl. Cryst. 37, 335-338.

ORTEP-3: Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565.

PLATON: Spek, A. L. (2003). J. Appl. Cryst. 36, 7-13.

publCIF: Westrip, S. P. (2008). publCIF. In preparation.

SADABS, TWINABS: Bruker (2001). Program name. Bruker AXS Inc., Madison,
Wisconsin, USA. or Sheldrick, G. M. (1996). Program name. University of
G\=ottingen, Germany.

SHELX Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.

SIR92: Altomare, A., Cascarano, G., Giacovazzo, C., Guagliardi, A., Burla,
M. C., Polidori, G. & Camalli, M. (1994). J. Appl. Cryst. 27, 435.

SIR97: Altomare, A., Burla, M. C., Camalli, M., Cascarano, G. L.,
Giacovazzo, C., Guagliardi, A., Moliterni, A. G. G., Polidori, G. &
Spagna, R. (1999). J. Appl. Cryst. 32, 115-119.

SIR2002: Burla, M. C., Camalli, M., Carrozzini, B., Cascarano, G. L.,
Giacovazzo, C., Polidori, G. & Spagna, R. (2003). J. Appl. Cryst. 36, 1103.

SUPERFLIP Palatinus, L. & Chapuis, G. (2007) J. Appl. Cryst. 40, 786-790.

WinGX: Farrugia, L. J. (1999). J. Appl. Cryst. 32, 837-838.

;
_publ_requested_category         FO
loop_
_publ_author_name
'D.B.G. Williams'
'S. Simelane'
'H.H. Kinfe'
'B. Owaga'

#------------------ SECTION 2. COMPOUND(S) DETAILS -------------------------#

data_mo_10bo_sand5_0m
_database_code_depnum_ccdc_archive 'CCDC 834632'
#TrackingRef '6289_web_deposit_cif_file_0_BernardOmondi_1310641264.archive.cif'

_audit_creation_date             2010-10-05T20:47:41-00:00
_audit_creation_method           'WinGX routine CIF_UPDATE'
_audit_conform_dict_name         cif_core.dic
_audit_conform_dict_version      2.4
_audit_conform_dict_location     ftp://ftp.iucr.org/pub/cif_core.dic

#----------------------------------------------------------------------------#
# CHEMICAL INFORMATION #
#----------------------------------------------------------------------------#

_chemical_name_systematic        
;
?
;
_chemical_formula_moiety         'C20 H20 O6'
_chemical_formula_sum            'C20 H20 O6'
_chemical_formula_weight         356.36
_chemical_absolute_configuration unk

#----------------------------------------------------------------------------#
# UNIT CELL INFORMATION #
#----------------------------------------------------------------------------#

_symmetry_cell_setting           monoclinic
_symmetry_space_group_name_H-M   C2
_symmetry_space_group_name_Hall  'C 2y'
loop_
_symmetry_equiv_pos_as_xyz
'x, y, z'
'-x, y, -z'
'x+1/2, y+1/2, z'
'-x+1/2, y+1/2, -z'

_cell_length_a                   25.7271(18)
_cell_length_b                   5.6497(4)
_cell_length_c                   13.2772(9)
_cell_angle_alpha                90
_cell_angle_beta                 112.4100(10)
_cell_angle_gamma                90
_cell_volume                     1784.1(2)
_cell_formula_units_Z            4
_cell_measurement_temperature    100(2)
_cell_measurement_reflns_used    33930
_cell_measurement_theta_min      1.66
_cell_measurement_theta_max      28.45

#----------------------------------------------------------------------------#
# CRYSTAL INFORMATION #
#----------------------------------------------------------------------------#

_exptl_crystal_description       block
_exptl_crystal_colour            colourless
_exptl_crystal_size_max          0.5
_exptl_crystal_size_mid          0.16
_exptl_crystal_size_min          0.1
_exptl_crystal_density_diffrn    1.327
_exptl_crystal_density_method    'not measured'
_exptl_crystal_F_000             752
_exptl_special_details           
;
The methyl, methylene, methine and aromatic H atoms were placed in
geometrically idealized positions and constrained to ride on their parent
atoms, with C---H = 0.95 \%A for aromatic, C---H = 0.99 \%A for methylene,
C---H = 1.00 \%A for mithine, C---H = 0.98 for Me and C---H = 0.84 for
OH groups.
;

#----------------------------------------------------------------------------#
# ABSORPTION CORRECTION #
#----------------------------------------------------------------------------#

_exptl_absorpt_coefficient_mu    0.098
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   'SADABS (Bruker, 2008)'
_exptl_absorpt_correction_T_min  0.9345
_exptl_absorpt_correction_T_max  0.9903

#----------------------------------------------------------------------------#
# DATA COLLECTION #
#----------------------------------------------------------------------------#

_diffrn_ambient_temperature      100(2)
_diffrn_radiation_wavelength     0.71073
_diffrn_radiation_type           MoK\a
_diffrn_radiation_monochromator  graphite
_diffrn_measurement_device_type  'Bruker X8 ApexII 4K Kappa CCD'
_diffrn_measurement_method       '\f and \w scans'
_diffrn_standards_number         0
_diffrn_standards_interval_count 0
_diffrn_standards_interval_time  0
_diffrn_standards_decay_%        0
_diffrn_reflns_av_R_equivalents  0.0262
_diffrn_reflns_av_unetI/netI     0.0139
_diffrn_reflns_number            33930
_diffrn_reflns_limit_h_min       -34
_diffrn_reflns_limit_h_max       34
_diffrn_reflns_limit_k_min       -7
_diffrn_reflns_limit_k_max       7
_diffrn_reflns_limit_l_min       -17
_diffrn_reflns_limit_l_max       17
_diffrn_reflns_theta_min         1.66
_diffrn_reflns_theta_max         28.45
_diffrn_reflns_theta_full        28.45
_diffrn_measured_fraction_theta_full 1
_diffrn_measured_fraction_theta_max 1
_reflns_number_total             4465
_reflns_number_gt                4362
_reflns_threshold_expression     >2sigma(I)

#----------------------------------------------------------------------------#
# COMPUTER PROGRAMS USED #
#----------------------------------------------------------------------------#

_computing_data_collection       'APEX2 (Bruker, 2007)'
_computing_cell_refinement       'SAINT-plus (Bruker, 2007)'
_computing_data_reduction        'SAINT-Plus and XPREP (Bruker, 2007)'
_computing_structure_solution    'SHELXS-97 (Sheldrick, 2008)'
_computing_structure_refinement  'SHELXL-97 (Sheldrick, 2008)'
_computing_molecular_graphics    'ORTEP3 (Farrugia, 1997)'
_computing_publication_material  'WinGX (Farrugia, 1999)'

#----------------------------------------------------------------------------#
# STRUCTURE SOLUTION
#----------------------------------------------------------------------------#

_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
_atom_sites_solution_hydrogens   geom

#----------------------------------------------------------------------------#
# REFINEMENT INFORMATION #
#----------------------------------------------------------------------------#

_refine_special_details          
;
Refinement of F^2^ against ALL reflections. The weighted R-factor wR and
goodness of fit S are based on F^2^, conventional R-factors R are based
on F, with F set to zero for negative F^2^. The threshold expression of
F^2^ > 2sigma(F^2^) is used only for calculating R-factors(gt) etc. and is
not relevant to the choice of reflections for refinement. R-factors based
on F^2^ are statistically about twice as large as those based on F, and R-
factors based on ALL data will be even larger.
The Following Model and Quality ALERTS were generated - (Acta-Mode) <<<
Format: alert-number_ALERT_alert-type_alert-level text
917_ALERT_2_G The FCF is likely NOT based on a BASF/TWIN Flack !
960_ALERT_3_G Number of Intensities with I .LT. - 2*sig(I) .. 1
024_ALERT_4_C Merging of Friedel Pairs is Indicated .......... !
791_ALERT_4_G Note: The Model has Chirality at C11 (Verify) R
791_ALERT_4_G Note: The Model has Chirality at C14 (Verify) S
791_ALERT_4_G Note: The Model has Chirality at C15 (Verify) R
Chirality checked, okay.
;
_refine_ls_structure_factor_coef Fsqd
_refine_ls_matrix_type           full
_refine_ls_weighting_scheme      calc
_refine_ls_weighting_details     
'calc w=1/[\s^2^(Fo^2^)+(0.0538P)^2^+0.4878P] where P=(Fo^2^+2Fc^2^)/3'
_refine_ls_hydrogen_treatment    constr
_refine_ls_extinction_method     none
_refine_ls_number_reflns         4465
_refine_ls_number_parameters     238
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0299
_refine_ls_R_factor_gt           0.0291
_refine_ls_wR_factor_ref         0.0794
_refine_ls_wR_factor_gt          0.0782
_refine_ls_goodness_of_fit_ref   1.024
_refine_ls_restrained_S_all      1.024
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0
_refine_ls_abs_structure_details 'Flack H D (1983), Acta Cryst. A39, 876-881'
_refine_ls_abs_structure_Flack   0.2(5)
_refine_diff_density_max         0.292
_refine_diff_density_min         -0.168
_refine_diff_density_rms         0.036

#----------------------------------------------------------------------------#
# ATOMIC TYPES, COORDINATES AND THERMAL PARAMETERS #
#----------------------------------------------------------------------------#

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 0 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.006 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

loop_
_atom_site_label
_atom_site_type_symbol
_atom_site_fract_x
_atom_site_fract_y
_atom_site_fract_z
_atom_site_U_iso_or_equiv
_atom_site_adp_type
_atom_site_occupancy
_atom_site_symmetry_multiplicity
_atom_site_calc_flag
_atom_site_refinement_flags
_atom_site_disorder_assembly
_atom_site_disorder_group
C1 C 0.77394(4) 0.50094(18) 0.83561(8) 0.01658(19) Uani 1 1 d . . .
C2 C 0.83099(4) 0.52979(19) 0.91118(8) 0.01814(19) Uani 1 1 d . . .
C3 C 0.86617(4) 0.7165(2) 0.90256(8) 0.0211(2) Uani 1 1 d . . .
H3 H 0.8516 0.8295 0.8457 0.025 Uiso 1 1 calc R . .
C4 C 0.92100(5) 0.7365(2) 0.97514(9) 0.0271(2) Uani 1 1 d . . .
H4 H 0.9437 0.8626 0.9678 0.033 Uiso 1 1 calc R . .
C5 C 0.94374(5) 0.5708(3) 1.06047(10) 0.0322(3) Uani 1 1 d . . .
H5 H 0.9816 0.5856 1.1103 0.039 Uiso 1 1 calc R . .
C6 C 0.91103(5) 0.3892(3) 1.07105(9) 0.0294(3) Uani 1 1 d . . .
H6 H 0.9265 0.2791 1.129 0.035 Uiso 1 1 calc R . .
C7 C 0.85432(5) 0.3618(2) 0.99700(9) 0.0223(2) Uani 1 1 d . . .
C8 C 0.82094(5) 0.1700(2) 1.00603(9) 0.0253(2) Uani 1 1 d . . .
H8 H 0.8362 0.0589 1.0635 0.03 Uiso 1 1 calc R . .
C9 C 0.76713(5) 0.1434(2) 0.93303(9) 0.0238(2) Uani 1 1 d . . .
H9 H 0.7453 0.013 0.9396 0.029 Uiso 1 1 calc R . .
C10 C 0.74339(4) 0.30884(19) 0.84720(8) 0.0195(2) Uani 1 1 d . . .
C11 C 0.74957(4) 0.67563(18) 0.74220(8) 0.01631(18) Uani 1 1 d . . .
H11 H 0.7675 0.8338 0.766 0.02 Uiso 1 1 calc R . .
C12 C 0.76062(4) 0.59572(19) 0.64380(8) 0.01876(19) Uani 1 1 d . . .
H12 H 0.7982 0.5616 0.6521 0.023 Uiso 1 1 calc R . .
C13 C 0.71996(4) 0.5710(2) 0.54599(8) 0.01907(19) Uani 1 1 d . . .
H13 H 0.7289 0.5119 0.4876 0.023 Uiso 1 1 calc R . .
C14 C 0.66016(4) 0.63451(19) 0.52574(7) 0.01670(18) Uani 1 1 d . . .
H14 H 0.6376 0.4883 0.5219 0.02 Uiso 1 1 calc R . .
C15 C 0.65802(4) 0.79842(19) 0.61557(8) 0.01653(18) Uani 1 1 d . . .
H15 H 0.6743 0.956 0.6095 0.02 Uiso 1 1 calc R . .
C16 C 0.59955(4) 0.83157(19) 0.61471(9) 0.0195(2) Uani 1 1 d . . .
H16A H 0.6005 0.9382 0.6745 0.023 Uiso 1 1 calc R . .
H16B H 0.5744 0.9011 0.5446 0.023 Uiso 1 1 calc R . .
C17 C 0.53020(4) 0.5896(2) 0.64081(8) 0.0200(2) Uani 1 1 d . . .
C18 C 0.51613(6) 0.3416(3) 0.66131(13) 0.0357(3) Uani 1 1 d . . .
H18A H 0.4789 0.3391 0.6656 0.054 Uiso 1 1 calc R . .
H18B H 0.5444 0.2845 0.7301 0.054 Uiso 1 1 calc R . .
H18C H 0.5159 0.2391 0.6016 0.054 Uiso 1 1 calc R . .
C19 C 0.61336(4) 0.6414(2) 0.33291(8) 0.0206(2) Uani 1 1 d . . .
C20 C 0.58532(5) 0.7977(2) 0.23589(9) 0.0268(2) Uani 1 1 d . . .
H20A H 0.5456 0.7541 0.2008 0.04 Uiso 1 1 calc R . .
H20B H 0.6038 0.778 0.184 0.04 Uiso 1 1 calc R . .
H20C H 0.5883 0.9633 0.2595 0.04 Uiso 1 1 calc R . .
O1 O 0.68906(3) 0.26116(16) 0.77925(6) 0.02476(17) Uani 1 1 d . . .
H1 H 0.6747 0.3824 0.7426 0.037 Uiso 1 1 calc R . .
O2 O 0.69027(3) 0.69449(14) 0.71866(5) 0.01755(15) Uani 1 1 d . . .
O3 O 0.57997(3) 0.59824(14) 0.62929(7) 0.02269(16) Uani 1 1 d . . .
O4 O 0.50203(3) 0.76262(16) 0.63592(7) 0.02538(17) Uani 1 1 d . . .
O5 O 0.63557(3) 0.77013(14) 0.42565(5) 0.01866(15) Uani 1 1 d . . .
O6 O 0.61632(4) 0.42907(17) 0.33075(7) 0.02775(18) Uani 1 1 d . . .

loop_
_atom_site_aniso_label
_atom_site_aniso_U_11
_atom_site_aniso_U_22
_atom_site_aniso_U_33
_atom_site_aniso_U_23
_atom_site_aniso_U_13
_atom_site_aniso_U_12
C1 0.0199(4) 0.0161(5) 0.0146(4) -0.0002(3) 0.0075(3) 0.0025(4)
C2 0.0201(4) 0.0201(5) 0.0148(4) -0.0003(3) 0.0072(3) 0.0055(4)
C3 0.0187(4) 0.0237(5) 0.0203(4) -0.0008(4) 0.0066(4) 0.0040(4)
C4 0.0195(5) 0.0324(6) 0.0273(5) -0.0040(5) 0.0066(4) 0.0022(4)
C5 0.0199(5) 0.0481(8) 0.0230(5) -0.0013(5) 0.0019(4) 0.0100(5)
C6 0.0267(5) 0.0409(7) 0.0179(5) 0.0053(5) 0.0056(4) 0.0145(5)
C7 0.0245(5) 0.0272(6) 0.0169(4) 0.0027(4) 0.0096(4) 0.0099(4)
C8 0.0356(6) 0.0234(6) 0.0214(5) 0.0078(4) 0.0159(4) 0.0120(4)
C9 0.0353(6) 0.0171(5) 0.0250(5) 0.0027(4) 0.0181(4) 0.0032(4)
C10 0.0249(5) 0.0180(5) 0.0177(4) -0.0022(4) 0.0104(4) 0.0013(4)
C11 0.0143(4) 0.0169(5) 0.0169(4) 0.0003(3) 0.0049(3) 0.0009(3)
C12 0.0174(4) 0.0211(5) 0.0197(4) 0.0032(4) 0.0093(4) 0.0033(4)
C13 0.0214(4) 0.0204(5) 0.0178(4) 0.0015(4) 0.0101(4) 0.0048(4)
C14 0.0170(4) 0.0174(5) 0.0147(4) 0.0015(3) 0.0051(3) 0.0017(3)
C15 0.0155(4) 0.0165(5) 0.0167(4) 0.0003(3) 0.0052(3) 0.0023(4)
C16 0.0170(4) 0.0171(5) 0.0247(5) 0.0006(4) 0.0084(4) 0.0023(4)
C17 0.0168(4) 0.0244(5) 0.0188(4) 0.0011(4) 0.0067(3) 0.0025(4)
C18 0.0290(6) 0.0268(6) 0.0594(8) 0.0100(6) 0.0260(6) 0.0040(5)
C19 0.0166(4) 0.0278(6) 0.0176(4) 0.0005(4) 0.0066(3) -0.0007(4)
C20 0.0232(5) 0.0359(7) 0.0189(4) 0.0065(4) 0.0054(4) -0.0013(5)
O1 0.0271(4) 0.0196(4) 0.0256(4) -0.0010(3) 0.0079(3) -0.0055(3)
O2 0.0154(3) 0.0213(4) 0.0160(3) 0.0010(3) 0.0060(2) 0.0034(3)
O3 0.0198(3) 0.0181(4) 0.0335(4) 0.0021(3) 0.0139(3) 0.0031(3)
O4 0.0207(3) 0.0256(4) 0.0317(4) 0.0010(3) 0.0121(3) 0.0045(3)
O5 0.0181(3) 0.0199(4) 0.0157(3) 0.0027(3) 0.0039(2) 0.0000(3)
O6 0.0332(4) 0.0266(4) 0.0210(4) -0.0037(3) 0.0076(3) 0.0004(3)

#----------------------------------------------------------------------------#
# MOLECULAR GEOMETRY #
#----------------------------------------------------------------------------#

_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_distance
_geom_bond_site_symmetry_2
_geom_bond_publ_flag
C1 C10 1.3826(15) . ?
C1 C2 1.4368(13) . ?
C1 C11 1.5207(13) . ?
C2 C3 1.4228(15) . ?
C2 C7 1.4277(14) . ?
C3 C4 1.3763(14) . ?
C3 H3 0.95 . ?
C4 C5 1.4129(18) . ?
C4 H4 0.95 . ?
C5 C6 1.368(2) . ?
C5 H5 0.95 . ?
C6 C7 1.4232(16) . ?
C6 H6 0.95 . ?
C7 C8 1.4156(18) . ?
C8 C9 1.3620(17) . ?
C8 H8 0.95 . ?
C9 C10 1.4195(15) . ?
C9 H9 0.95 . ?
C10 O1 1.3706(13) . ?
C11 O2 1.4397(11) . ?
C11 C12 1.5082(13) . ?
C11 H11 1 . ?
C12 C13 1.3282(14) . ?
C12 H12 0.95 . ?
C13 C14 1.5009(13) . ?
C13 H13 0.95 . ?
C14 O5 1.4534(11) . ?
C14 C15 1.5274(13) . ?
C14 H14 1 . ?
C15 O2 1.4286(11) . ?
C15 C16 1.5115(13) . ?
C15 H15 1 . ?
C16 O3 1.4503(13) . ?
C16 H16A 0.99 . ?
C16 H16B 0.99 . ?
C17 O4 1.2040(14) . ?
C17 O3 1.3470(12) . ?
C17 C18 1.4973(18) . ?
C18 H18A 0.98 . ?
C18 H18B 0.98 . ?
C18 H18C 0.98 . ?
C19 O6 1.2031(16) . ?
C19 O5 1.3547(13) . ?
C19 C20 1.5004(15) . ?
C20 H20A 0.98 . ?
C20 H20B 0.98 . ?
C20 H20C 0.98 . ?
O1 H1 0.84 . ?

loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
_geom_angle_site_symmetry_1
_geom_angle_site_symmetry_3
_geom_angle_publ_flag
C10 C1 C2 118.94(9) . . ?
C10 C1 C11 121.67(9) . . ?
C2 C1 C11 119.33(9) . . ?
C3 C2 C7 118.06(9) . . ?
C3 C2 C1 122.66(9) . . ?
C7 C2 C1 119.25(10) . . ?
C4 C3 C2 121.20(10) . . ?
C4 C3 H3 119.4 . . ?
C2 C3 H3 119.4 . . ?
C3 C4 C5 120.52(12) . . ?
C3 C4 H4 119.7 . . ?
C5 C4 H4 119.7 . . ?
C6 C5 C4 119.76(11) . . ?
C6 C5 H5 120.1 . . ?
C4 C5 H5 120.1 . . ?
C5 C6 C7 121.29(11) . . ?
C5 C6 H6 119.4 . . ?
C7 C6 H6 119.4 . . ?
C8 C7 C6 121.34(10) . . ?
C8 C7 C2 119.49(10) . . ?
C6 C7 C2 119.17(11) . . ?
C9 C8 C7 120.61(10) . . ?
C9 C8 H8 119.7 . . ?
C7 C8 H8 119.7 . . ?
C8 C9 C10 120.53(10) . . ?
C8 C9 H9 119.7 . . ?
C10 C9 H9 119.7 . . ?
O1 C10 C1 124.15(9) . . ?
O1 C10 C9 114.69(10) . . ?
C1 C10 C9 121.16(10) . . ?
O2 C11 C12 111.60(8) . . ?
O2 C11 C1 107.36(7) . . ?
C12 C11 C1 110.91(8) . . ?
O2 C11 H11 109 . . ?
C12 C11 H11 109 . . ?
C1 C11 H11 109 . . ?
C13 C12 C11 122.70(9) . . ?
C13 C12 H12 118.7 . . ?
C11 C12 H12 118.7 . . ?
C12 C13 C14 121.43(9) . . ?
C12 C13 H13 119.3 . . ?
C14 C13 H13 119.3 . . ?
O5 C14 C13 110.42(8) . . ?
O5 C14 C15 105.17(8) . . ?
C13 C14 C15 110.16(8) . . ?
O5 C14 H14 110.3 . . ?
C13 C14 H14 110.3 . . ?
C15 C14 H14 110.3 . . ?
O2 C15 C16 105.72(7) . . ?
O2 C15 C14 108.56(8) . . ?
C16 C15 C14 113.65(8) . . ?
O2 C15 H15 109.6 . . ?
C16 C15 H15 109.6 . . ?
C14 C15 H15 109.6 . . ?
O3 C16 C15 106.36(8) . . ?
O3 C16 H16A 110.5 . . ?
C15 C16 H16A 110.5 . . ?
O3 C16 H16B 110.5 . . ?
C15 C16 H16B 110.5 . . ?
H16A C16 H16B 108.6 . . ?
O4 C17 O3 122.89(10) . . ?
O4 C17 C18 125.95(10) . . ?
O3 C17 C18 111.15(9) . . ?
C17 C18 H18A 109.5 . . ?
C17 C18 H18B 109.5 . . ?
H18A C18 H18B 109.5 . . ?
C17 C18 H18C 109.5 . . ?
H18A C18 H18C 109.5 . . ?
H18B C18 H18C 109.5 . . ?
O6 C19 O5 123.25(10) . . ?
O6 C19 C20 125.50(11) . . ?
O5 C19 C20 111.25(10) . . ?
C19 C20 H20A 109.5 . . ?
C19 C20 H20B 109.5 . . ?
H20A C20 H20B 109.5 . . ?
C19 C20 H20C 109.5 . . ?
H20A C20 H20C 109.5 . . ?
H20B C20 H20C 109.5 . . ?
C10 O1 H1 109.5 . . ?
C15 O2 C11 114.75(7) . . ?
C17 O3 C16 116.22(8) . . ?
C19 O5 C14 115.71(8) . . ?

loop_
_geom_torsion_atom_site_label_1
_geom_torsion_atom_site_label_2
_geom_torsion_atom_site_label_3
_geom_torsion_atom_site_label_4
_geom_torsion
_geom_torsion_site_symmetry_1
_geom_torsion_site_symmetry_2
_geom_torsion_site_symmetry_3
_geom_torsion_site_symmetry_4
_geom_torsion_publ_flag
C10 C1 C2 C3 177.30(9) . . . . ?
C11 C1 C2 C3 -0.01(14) . . . . ?
C10 C1 C2 C7 -0.91(13) . . . . ?
C11 C1 C2 C7 -178.23(9) . . . . ?
C7 C2 C3 C4 -0.51(15) . . . . ?
C1 C2 C3 C4 -178.74(10) . . . . ?
C2 C3 C4 C5 -0.01(17) . . . . ?
C3 C4 C5 C6 0.01(18) . . . . ?
C4 C5 C6 C7 0.52(18) . . . . ?
C5 C6 C7 C8 178.19(11) . . . . ?
C5 C6 C7 C2 -1.04(16) . . . . ?
C3 C2 C7 C8 -178.23(9) . . . . ?
C1 C2 C7 C8 0.07(14) . . . . ?
C3 C2 C7 C6 1.01(14) . . . . ?
C1 C2 C7 C6 179.31(10) . . . . ?
C6 C7 C8 C9 -178.51(10) . . . . ?
C2 C7 C8 C9 0.71(15) . . . . ?
C7 C8 C9 C10 -0.64(16) . . . . ?
C2 C1 C10 O1 -178.99(9) . . . . ?
C11 C1 C10 O1 -1.74(15) . . . . ?
C2 C1 C10 C9 1.01(14) . . . . ?
C11 C1 C10 C9 178.26(9) . . . . ?
C8 C9 C10 O1 179.76(10) . . . . ?
C8 C9 C10 C1 -0.24(15) . . . . ?
C10 C1 C11 O2 33.83(12) . . . . ?
C2 C1 C11 O2 -148.93(8) . . . . ?
C10 C1 C11 C12 -88.33(11) . . . . ?
C2 C1 C11 C12 88.91(11) . . . . ?
O2 C11 C12 C13 6.39(15) . . . . ?
C1 C11 C12 C13 126.05(11) . . . . ?
C11 C12 C13 C14 3.40(17) . . . . ?
C12 C13 C14 O5 134.72(10) . . . . ?
C12 C13 C14 C15 18.99(14) . . . . ?
O5 C14 C15 O2 -169.92(7) . . . . ?
C13 C14 C15 O2 -50.94(10) . . . . ?
O5 C14 C15 C16 72.75(10) . . . . ?
C13 C14 C15 C16 -168.27(9) . . . . ?
O2 C15 C16 O3 -59.17(10) . . . . ?
C14 C15 C16 O3 59.80(10) . . . . ?
C16 C15 O2 C11 -172.38(8) . . . . ?
C14 C15 O2 C11 65.34(10) . . . . ?
C12 C11 O2 C15 -41.88(11) . . . . ?
C1 C11 O2 C15 -163.61(8) . . . . ?
O4 C17 O3 C16 2.39(14) . . . . ?
C18 C17 O3 C16 -176.88(10) . . . . ?
C15 C16 O3 C17 174.24(8) . . . . ?
O6 C19 O5 C14 -4.39(14) . . . . ?
C20 C19 O5 C14 175.65(8) . . . . ?
C13 C14 O5 C19 85.35(10) . . . . ?
C15 C14 O5 C19 -155.84(8) . . . . ?

# END of CIF