# Electronic Supplementary Material (ESI) for Organic Chemistry Frontiers.
# This journal is © the Partner Organisations 2019

####################################################################### 
# 
# This file contains crystal structure data downloaded from the 
# Cambridge Structural Database (CSD) hosted by the Cambridge 
# Crystallographic Data Centre (CCDC).
# 
# Full information about CCDC data access policies and citation 
# guidelines are available at http://www.ccdc.cam.ac.uk/access/V1 
# 
# Audit and citation data items may have been added by the CCDC. 
# Please retain this information to preserve the provenance of 
# this file and to allow appropriate attribution of the data. 
# 
#######################################################################

data_lq-zx-180418
_database_code_depnum_ccdc_archive 'CCDC 1905940'
loop_
_audit_author_name
_audit_author_address
'Qingsong Dai'
;Sichuan industrial institute of antibiotics chengdu university
China
;
_audit_update_record             
;
2019-03-27 deposited with the CCDC.	2019-05-08 downloaded from the CCDC.
;
_audit_creation_date             2018-04-19
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.04.03 svn.r3497 for OlexSys, GUI svn.r5486)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C20 H21 N3 O4'
_chemical_formula_sum            'C20 H21 N3 O4'
_chemical_formula_weight         367.40
_chemical_melting_point          ?
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0181 0.0091 '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'
N N 0.0311 0.0180 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0492 0.0322 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_shelx_space_group_comment       
;
The symmetry employed for this shelxl refinement is uniquely defined
by the following loop, which should always be used as a source of
symmetry information in preference to the above space-group names.
They are only intended as comments.
;
_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 1 21/n 1'
_space_group_name_Hall           '-P 2yn'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, y+1/2, -z+1/2'
'-x, -y, -z'
'x-1/2, -y-1/2, z-1/2'

_cell_length_a                   10.8238(4)
_cell_length_b                   10.3557(3)
_cell_length_c                   17.8199(7)
_cell_angle_alpha                90
_cell_angle_beta                 96.908(3)
_cell_angle_gamma                90
_cell_volume                     1982.89(12)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    4101
_cell_measurement_temperature    295.91(10)
_cell_measurement_theta_max      72.3310
_cell_measurement_theta_min      4.0970
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    0.715
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.05370
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            'clear light colourless'
_exptl_crystal_colour_lustre     clear
_exptl_crystal_colour_modifier   light
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    1.231
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             776
_exptl_crystal_size_max          0.7
_exptl_crystal_size_mid          0.6
_exptl_crystal_size_min          0.4
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0237
_diffrn_reflns_av_unetI/netI     0.0228
_diffrn_reflns_Laue_measured_fraction_full 0.999
_diffrn_reflns_Laue_measured_fraction_max 0.981
_diffrn_reflns_limit_h_max       13
_diffrn_reflns_limit_h_min       -13
_diffrn_reflns_limit_k_max       12
_diffrn_reflns_limit_k_min       -8
_diffrn_reflns_limit_l_max       17
_diffrn_reflns_limit_l_min       -21
_diffrn_reflns_number            10517
_diffrn_reflns_point_group_measured_fraction_full 0.999
_diffrn_reflns_point_group_measured_fraction_max 0.981
_diffrn_reflns_theta_full        67.684
_diffrn_reflns_theta_max         72.365
_diffrn_reflns_theta_min         5.000
_diffrn_ambient_environment      air
_diffrn_ambient_temperature      295.91(10)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 15.9595
_diffrn_detector_type            EosS2
_diffrn_measured_fraction_theta_full 0.999
_diffrn_measured_fraction_theta_max 0.981
_diffrn_measurement_details      
;
#__ type_ start__ end____ width___ exp.time_
  1 omega    1.00   75.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671  -99.0000    0.0000 74

#__ type_ start__ end____ width___ exp.time_
  2 omega    9.00  104.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671   77.0000 -120.0000 95

#__ type_ start__ end____ width___ exp.time_
  3 omega   23.00   90.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671 -125.0000  -60.0000 67

#__ type_ start__ end____ width___ exp.time_
  4 omega  -31.00   53.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671  -57.0000  -90.0000 84

#__ type_ start__ end____ width___ exp.time_
  5 omega    9.00  104.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671   77.0000   30.0000 95

#__ type_ start__ end____ width___ exp.time_
  6 omega    9.00  104.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671   77.0000  120.0000 95

#__ type_ start__ end____ width___ exp.time_
  7 omega   38.00   91.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000  -60.0000 53

#__ type_ start__ end____ width___ exp.time_
  8 omega   38.00   91.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000 -180.0000 53

#__ type_ start__ end____ width___ exp.time_
  9 omega   38.00   91.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000 -120.0000 53

#__ type_ start__ end____ width___ exp.time_
 10 omega   38.00   91.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000  -90.0000 53

#__ type_ start__ end____ width___ exp.time_
 11 omega   39.00  109.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -94.0000 -180.0000 70

#__ type_ start__ end____ width___ exp.time_
 12 omega   39.00  109.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -94.0000  -90.0000 70

#__ type_ start__ end____ width___ exp.time_
 13 omega   38.00   91.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -30.0000  -30.0000 53

#__ type_ start__ end____ width___ exp.time_
 14 omega   91.00  176.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000   45.0000   60.0000 85

#__ type_ start__ end____ width___ exp.time_
 15 omega   39.00  109.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -94.0000 -150.0000 70

#__ type_ start__ end____ width___ exp.time_
 16 omega   40.00  135.00   1.0000    1.1700
omega____ theta____ kappa____ phi______ frames
    -      108.0000  -77.0000  -60.0000 95

#__ type_ start__ end____ width___ exp.time_
 17 omega    9.00   34.00   1.0000    1.0000
omega____ theta____ kappa____ phi______ frames
    -       36.1671   77.0000  -30.0000 25
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'New Gemini, Dual, Cu at zero, EosS2'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_UB_11      -0.0787360000
_diffrn_orient_matrix_UB_12      -0.0462093000
_diffrn_orient_matrix_UB_13      -0.0728506000
_diffrn_orient_matrix_UB_21      -0.1181410000
_diffrn_orient_matrix_UB_22      0.0061397000
_diffrn_orient_matrix_UB_23      0.0402480000
_diffrn_orient_matrix_UB_31      -0.0205462000
_diffrn_orient_matrix_UB_32      0.1412033000
_diffrn_orient_matrix_UB_33      -0.0255989000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           CuK\a
_diffrn_radiation_wavelength     1.54184
_diffrn_source                   'Enhance (Cu) X-ray Source'
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                3290
_reflns_number_total             3854
_reflns_odcompleteness_completeness 99.87
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     66.97
_reflns_special_details          
;
 Reflections were merged by SHELXL according to the crystal
 class for the calculation of statistics and refinement.
 
 _reflns_Friedel_fraction is defined as the number of unique
 Friedel pairs measured divided by the number that would be
 possible theoretically, ignoring centric projections and
 systematic absences.
;
_reflns_threshold_expression     'I > 2σ(I)'
_computing_cell_refinement       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_collection       
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_data_reduction        
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.35 (release 13-08-2014 CrysAlis171 .NET)
(compiled Aug 13 2014,18:06:01)
;
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXT (Sheldrick, 2015)'
_refine_diff_density_max         0.297
_refine_diff_density_min         -0.410
_refine_diff_density_rms         0.116
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.072
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     248
_refine_ls_number_reflns         3854
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0737
_refine_ls_R_factor_gt           0.0671
_refine_ls_restrained_S_all      1.072
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.1160P)²+0.2070P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1697
_refine_ls_wR_factor_ref         0.1800
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Secondary CH2 refined with riding coordinates:
 C1(H1A,H1B), C14(H14A,H14B)
2.b Aromatic/amide H refined with riding coordinates:
 C12(H12), C8(H8), C9(H9), C10(H10), C11(H11)
2.c Idealised Me refined as rotating group:
 C18(H18A,H18B,H18C), C20(H20A,H20B,H20C), C19(H19A,H19B,H19C), C15(H15A,H15B,
 H15C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   ?
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_site_symmetry_order
_atom_site_calc_flag
_atom_site_refinement_flags_posn
_atom_site_refinement_flags_adp
_atom_site_refinement_flags_occupancy
_atom_site_disorder_assembly
_atom_site_disorder_group
O4 O 0.20760(13) 0.55327(12) 0.60907(7) 0.0586(4) Uani 1 1 d . . . . .
O3 O 0.11201(14) 0.40054(13) 0.67272(7) 0.0613(4) Uani 1 1 d . . . . .
O1 O 0.15904(13) 0.60778(13) 0.44553(8) 0.0631(4) Uani 1 1 d . . . . .
O2 O 0.35823(12) 0.54556(12) 0.46856(9) 0.0612(4) Uani 1 1 d . . . . .
N1 N 0.14903(14) 0.37064(13) 0.55196(8) 0.0495(4) Uani 1 1 d . . . . .
C13 C 0.23717(15) 0.53025(14) 0.46537(8) 0.0423(4) Uani 1 1 d . . . . .
C4 C 0.20803(14) 0.39446(14) 0.48775(8) 0.0401(3) Uani 1 1 d . . . . .
C7 C 0.27544(14) 0.27260(15) 0.37587(9) 0.0434(4) Uani 1 1 d . . . . .
N3 N 0.0521(2) 0.00586(19) 0.40692(12) 0.0876(7) Uani 1 1 d . . . . .
C3 C 0.22574(14) 0.28742(15) 0.44852(8) 0.0414(3) Uani 1 1 d . . . . .
C16 C 0.15327(15) 0.44099(15) 0.61747(9) 0.0451(4) Uani 1 1 d . . . . .
C2 C 0.18250(17) 0.17195(15) 0.49369(9) 0.0497(4) Uani 1 1 d . . . . .
C6 C 0.1099(2) 0.07712(17) 0.44478(11) 0.0587(5) Uani 1 1 d . . . . .
C12 C 0.24821(17) 0.36316(18) 0.31870(10) 0.0528(4) Uani 1 1 d . . . . .
H12 H 0.1972 0.4331 0.3262 0.063 Uiso 1 1 calc R . . . .
C8 C 0.35080(17) 0.16791(18) 0.36254(11) 0.0570(5) Uani 1 1 d . . . . .
H8 H 0.3697 0.1059 0.3999 0.068 Uiso 1 1 calc R . . . .
C1 C 0.10051(19) 0.23908(16) 0.54792(10) 0.0561(5) Uani 1 1 d . . . . .
H1A H 0.0133 0.2375 0.5275 0.067 Uiso 1 1 calc R . . . .
H1B H 0.1102 0.1984 0.5973 0.067 Uiso 1 1 calc R . . . .
C17 C 0.22376(19) 0.64953(17) 0.67059(10) 0.0550(4) Uani 1 1 d . . . . .
C5 C 0.2910(2) 0.10656(19) 0.53584(12) 0.0675(6) Uani 1 1 d . . . . .
C9 C 0.39766(19) 0.1558(2) 0.29382(13) 0.0669(6) Uani 1 1 d . . . . .
H9 H 0.4476 0.0854 0.2854 0.080 Uiso 1 1 calc R . . . .
C10 C 0.37103(19) 0.2467(2) 0.23805(12) 0.0690(6) Uani 1 1 d . . . . .
H10 H 0.4032 0.2385 0.1922 0.083 Uiso 1 1 calc R . . . .
C11 C 0.2965(2) 0.3499(2) 0.25064(11) 0.0679(5) Uani 1 1 d . . . . .
H11 H 0.2783 0.4116 0.2130 0.082 Uiso 1 1 calc R . . . .
N2 N 0.3747(3) 0.0606(2) 0.57021(16) 0.1032(8) Uani 1 1 d . . . . .
C18 C 0.2813(3) 0.7617(2) 0.63287(14) 0.0853(8) Uani 1 1 d . . . . .
H18A H 0.3602 0.7358 0.6183 0.128 Uiso 1 1 calc GR . . . .
H18B H 0.2931 0.8328 0.6675 0.128 Uiso 1 1 calc GR . . . .
H18C H 0.2271 0.7875 0.5888 0.128 Uiso 1 1 calc GR . . . .
C14 C 0.4046(3) 0.6685(2) 0.44357(17) 0.0874(8) Uani 1 1 d . . . . .
H14A H 0.4660 0.7032 0.4825 0.105 Uiso 1 1 calc R . . . .
H14B H 0.3366 0.7298 0.4350 0.105 Uiso 1 1 calc R . . . .
C20 C 0.3119(3) 0.5949(3) 0.73487(15) 0.0959(9) Uani 1 1 d . . . . .
H20A H 0.2736 0.5226 0.7565 0.144 Uiso 1 1 calc GR . . . .
H20B H 0.3311 0.6602 0.7728 0.144 Uiso 1 1 calc GR . . . .
H20C H 0.3872 0.5673 0.7162 0.144 Uiso 1 1 calc GR . . . .
C19 C 0.1006(3) 0.6856(3) 0.6953(2) 0.0984(9) Uani 1 1 d . . . . .
H19A H 0.0428 0.7061 0.6518 0.148 Uiso 1 1 calc GR . . . .
H19B H 0.1110 0.7594 0.7281 0.148 Uiso 1 1 calc GR . . . .
H19C H 0.0692 0.6145 0.7219 0.148 Uiso 1 1 calc GR . . . .
C15 C 0.4608(3) 0.6501(3) 0.37373(18) 0.1003(9) Uani 1 1 d . . . . .
H15A H 0.3998 0.6156 0.3354 0.150 Uiso 1 1 calc GR . . . .
H15B H 0.5294 0.5910 0.3827 0.150 Uiso 1 1 calc GR . . . .
H15C H 0.4902 0.7315 0.3572 0.150 Uiso 1 1 calc GR . . . .


_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
O4 C16 1.3196(18) . ?
O4 C17 1.4765(19) . ?
O3 C16 1.2043(19) . ?
O1 C13 1.189(2) . ?
O2 C13 1.314(2) . ?
O2 C14 1.458(2) . ?
N1 C4 1.3978(18) . ?
N1 C16 1.372(2) . ?
N1 C1 1.4588(19) . ?
C13 C4 1.505(2) . ?
C4 C3 1.337(2) . ?
C7 C3 1.469(2) . ?
C7 C12 1.390(2) . ?
C7 C8 1.394(2) . ?
N3 C6 1.136(3) . ?
C3 C2 1.545(2) . ?
C2 C6 1.475(2) . ?
C2 C1 1.553(2) . ?
C2 C5 1.480(3) . ?
C12 H12 0.9300 . ?
C12 C11 1.384(2) . ?
C8 H8 0.9300 . ?
C8 C9 1.386(3) . ?
C1 H1A 0.9700 . ?
C1 H1B 0.9700 . ?
C17 C18 1.513(3) . ?
C17 C20 1.510(3) . ?
C17 C19 1.501(3) . ?
C5 N2 1.135(3) . ?
C9 H9 0.9300 . ?
C9 C10 1.375(3) . ?
C10 H10 0.9300 . ?
C10 C11 1.373(3) . ?
C11 H11 0.9300 . ?
C18 H18A 0.9600 . ?
C18 H18B 0.9600 . ?
C18 H18C 0.9600 . ?
C14 H14A 0.9700 . ?
C14 H14B 0.9700 . ?
C14 C15 1.462(4) . ?
C20 H20A 0.9600 . ?
C20 H20B 0.9600 . ?
C20 H20C 0.9600 . ?
C19 H19A 0.9600 . ?
C19 H19B 0.9600 . ?
C19 H19C 0.9600 . ?
C15 H15A 0.9600 . ?
C15 H15B 0.9600 . ?
C15 H15C 0.9600 . ?

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
C16 O4 C17 121.69(12) . . ?
C13 O2 C14 118.05(17) . . ?
C4 N1 C1 108.76(12) . . ?
C16 N1 C4 129.12(13) . . ?
C16 N1 C1 120.86(13) . . ?
O1 C13 O2 126.96(15) . . ?
O1 C13 C4 123.06(15) . . ?
O2 C13 C4 109.93(13) . . ?
N1 C4 C13 120.84(13) . . ?
C3 C4 N1 112.96(13) . . ?
C3 C4 C13 126.04(13) . . ?
C12 C7 C3 120.51(14) . . ?
C12 C7 C8 118.47(15) . . ?
C8 C7 C3 121.02(15) . . ?
C4 C3 C7 129.69(14) . . ?
C4 C3 C2 107.33(13) . . ?
C7 C3 C2 122.98(13) . . ?
O4 C16 N1 109.95(13) . . ?
O3 C16 O4 127.83(15) . . ?
O3 C16 N1 122.22(14) . . ?
C3 C2 C1 102.08(12) . . ?
C6 C2 C3 112.36(14) . . ?
C6 C2 C1 111.22(15) . . ?
C6 C2 C5 109.21(16) . . ?
C5 C2 C3 110.30(15) . . ?
C5 C2 C1 111.53(16) . . ?
N3 C6 C2 178.6(3) . . ?
C7 C12 H12 119.8 . . ?
C11 C12 C7 120.42(18) . . ?
C11 C12 H12 119.8 . . ?
C7 C8 H8 119.8 . . ?
C9 C8 C7 120.32(19) . . ?
C9 C8 H8 119.8 . . ?
N1 C1 C2 102.68(12) . . ?
N1 C1 H1A 111.2 . . ?
N1 C1 H1B 111.2 . . ?
C2 C1 H1A 111.2 . . ?
C2 C1 H1B 111.2 . . ?
H1A C1 H1B 109.1 . . ?
O4 C17 C18 101.93(14) . . ?
O4 C17 C20 108.55(17) . . ?
O4 C17 C19 110.86(18) . . ?
C20 C17 C18 111.6(2) . . ?
C19 C17 C18 111.5(2) . . ?
C19 C17 C20 111.9(2) . . ?
N2 C5 C2 177.1(3) . . ?
C8 C9 H9 119.7 . . ?
C10 C9 C8 120.61(19) . . ?
C10 C9 H9 119.7 . . ?
C9 C10 H10 120.3 . . ?
C11 C10 C9 119.43(18) . . ?
C11 C10 H10 120.3 . . ?
C12 C11 H11 119.6 . . ?
C10 C11 C12 120.8(2) . . ?
C10 C11 H11 119.6 . . ?
C17 C18 H18A 109.5 . . ?
C17 C18 H18B 109.5 . . ?
C17 C18 H18C 109.5 . . ?
H18A C18 H18B 109.5 . . ?
H18A C18 H18C 109.5 . . ?
H18B C18 H18C 109.5 . . ?
O2 C14 H14A 109.7 . . ?
O2 C14 H14B 109.7 . . ?
O2 C14 C15 109.8(2) . . ?
H14A C14 H14B 108.2 . . ?
C15 C14 H14A 109.7 . . ?
C15 C14 H14B 109.7 . . ?
C17 C20 H20A 109.5 . . ?
C17 C20 H20B 109.5 . . ?
C17 C20 H20C 109.5 . . ?
H20A C20 H20B 109.5 . . ?
H20A C20 H20C 109.5 . . ?
H20B C20 H20C 109.5 . . ?
C17 C19 H19A 109.5 . . ?
C17 C19 H19B 109.5 . . ?
C17 C19 H19C 109.5 . . ?
H19A C19 H19B 109.5 . . ?
H19A C19 H19C 109.5 . . ?
H19B C19 H19C 109.5 . . ?
C14 C15 H15A 109.5 . . ?
C14 C15 H15B 109.5 . . ?
C14 C15 H15C 109.5 . . ?
H15A C15 H15B 109.5 . . ?
H15A C15 H15C 109.5 . . ?
H15B C15 H15C 109.5 . . ?

_olex2_submission_special_instructions 'No special instructions were received'
