# Electronic Supplementary Material (ESI) for Organic Chemistry Frontiers.
# This journal is © the Partner Organisations 2017

####################################################################### 
# 
# 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. 
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#######################################################################

data_cu_d8v17020_0m
_database_code_depnum_ccdc_archive 'CCDC 1566708'
_audit_update_record             
;
2017-08-04 deposited with the CCDC.
2017-11-06 downloaded from the CCDC.
;
_audit_creation_date             2017-05-17
_audit_creation_method           
;
Olex2 1.2
(compiled 2017.03.28 svn.r3405 for OlexSys, GUI svn.r5335)
;
_shelx_SHELXL_version_number     2016/6
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C23 H25 N O2'
_chemical_formula_sum            'C23 H25 N O2'
_chemical_formula_weight         347.44
_chemical_absolute_configuration rmad
_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           5
_space_group_name_H-M_alt        'C 1 2 1'
_space_group_name_Hall           'C 2y'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, y, -z'
'x+1/2, y+1/2, z'
'-x+1/2, y+1/2, -z'

_cell_length_a                   17.0278(9)
_cell_length_b                   8.4534(5)
_cell_length_c                   14.6680(8)
_cell_angle_alpha                90
_cell_angle_beta                 110.034(2)
_cell_angle_gamma                90
_cell_volume                     1983.59(19)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    8702
_cell_measurement_temperature    301(2)
_cell_measurement_theta_max      70.11
_cell_measurement_theta_min      5.360
_shelx_estimated_absorpt_T_max   0.918
_shelx_estimated_absorpt_T_min   0.846
_exptl_absorpt_coefficient_mu    0.578
_exptl_absorpt_correction_T_max  0.7533
_exptl_absorpt_correction_T_min  0.5298
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2016/2 (Bruker,2016/2) was used for absorption correction. wR2(int) was 0.1466 before and 0.0857 after correction. The Ratio of minimum to maximum transmission is 0.7033. The λ/2 correction factor is Not present.'
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            colourless
_exptl_crystal_density_diffrn    1.163
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             744
_exptl_crystal_size_max          0.3
_exptl_crystal_size_mid          0.25
_exptl_crystal_size_min          0.15
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0492
_diffrn_reflns_av_unetI/netI     0.0438
_diffrn_reflns_Laue_measured_fraction_full 0.979
_diffrn_reflns_Laue_measured_fraction_max 0.976
_diffrn_reflns_limit_h_max       20
_diffrn_reflns_limit_h_min       -20
_diffrn_reflns_limit_k_max       10
_diffrn_reflns_limit_k_min       -10
_diffrn_reflns_limit_l_max       17
_diffrn_reflns_limit_l_min       -17
_diffrn_reflns_number            13417
_diffrn_reflns_point_group_measured_fraction_full 0.968
_diffrn_reflns_point_group_measured_fraction_max 0.964
_diffrn_reflns_theta_full        67.679
_diffrn_reflns_theta_max         70.161
_diffrn_reflns_theta_min         5.359
_diffrn_ambient_temperature      301.2
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.979
_diffrn_measured_fraction_theta_max 0.976
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_type           CuK\a
_diffrn_radiation_wavelength     1.54178
_diffrn_source                   ?
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.840
_reflns_Friedel_fraction_full    0.955
_reflns_Friedel_fraction_max     0.949
_reflns_number_gt                3230
_reflns_number_total             3654
_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       'SAINT v8.37A (Bruker, 2015)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT v8.37A (Bruker, 2015)'
_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         0.187
_refine_diff_density_min         -0.174
_refine_diff_density_rms         0.031
_refine_ls_abs_structure_details 
;
 Flack x determined using 1228 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_refine_ls_abs_structure_Flack   0.07(18)
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.048
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     238
_refine_ls_number_reflns         3654
_refine_ls_number_restraints     1
_refine_ls_R_factor_all          0.0703
_refine_ls_R_factor_gt           0.0640
_refine_ls_restrained_S_all      1.048
_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)+(0.1124P)²+0.3301P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1766
_refine_ls_wR_factor_ref         0.1844
_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 Ternary CH refined with riding coordinates:
 C1(H1)
2.b Secondary CH2 refined with riding coordinates:
 C9(H9A,H9B), C17(H17A,H17B)
2.c Aromatic/amide H refined with riding coordinates:
 C3(H3), C12(H12), C13(H13), C14(H14), C15(H15), C16(H16), C19(H19), C20(H20),
 C21(H21), C22(H22), C23(H23)
2.d Idealised Me refined as rotating group:
 C6(H6A,H6B,H6C), C7(H7A,H7B,H7C), C10(H10A,H10B,H10C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     dual
_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
O1 O -0.3619(3) -0.7181(8) -0.1185(5) 0.210(4) Uani 1 1 d . . . . .
O2 O -0.4627(3) -0.8211(5) -0.2373(3) 0.1379(16) Uani 1 1 d . . . . .
N1 N -0.61247(17) -0.3011(5) -0.2622(2) 0.0778(8) Uani 1 1 d . . . . .
C1 C -0.4338(2) -0.5537(5) -0.2530(3) 0.0735(9) Uani 1 1 d . . . . .
H1 H -0.451437 -0.584144 -0.321538 0.088 Uiso 1 1 calc R . . . .
C2 C -0.5064(2) -0.4673(4) -0.2385(2) 0.0702(8) Uani 1 1 d . . . . .
C3 C -0.5292(2) -0.4643(6) -0.1545(3) 0.0843(11) Uani 1 1 d . . . . .
H3 H -0.503729 -0.521869 -0.098071 0.101 Uiso 1 1 calc R . . . .
C4 C -0.5947(2) -0.3632(6) -0.1700(3) 0.0863(12) Uani 1 1 d . . . . .
C5 C -0.55872(19) -0.3655(5) -0.3042(2) 0.0693(8) Uani 1 1 d . . . . .
C6 C -0.5609(3) -0.3216(6) -0.4030(3) 0.0882(11) Uani 1 1 d . . . . .
H6A H -0.529066 -0.226680 -0.399617 0.132 Uiso 1 1 calc GR . . . .
H6B H -0.617741 -0.304004 -0.444032 0.132 Uiso 1 1 calc GR . . . .
H6C H -0.537335 -0.405690 -0.429328 0.132 Uiso 1 1 calc GR . . . .
C7 C -0.6411(3) -0.3168(10) -0.1042(4) 0.121(2) Uani 1 1 d . . . . .
H7A H -0.695693 -0.364076 -0.126572 0.182 Uiso 1 1 calc GR . . . .
H7B H -0.646519 -0.203743 -0.104150 0.182 Uiso 1 1 calc GR . . . .
H7C H -0.611009 -0.352714 -0.039512 0.182 Uiso 1 1 calc GR . . . .
C8 C -0.4128(3) -0.7053(6) -0.1937(4) 0.1001(15) Uani 1 1 d . . . . .
C9 C -0.4443(9) -0.9764(10) -0.1902(8) 0.220(6) Uani 1 1 d . . . . .
H9A H -0.466632 -1.059284 -0.237776 0.264 Uiso 1 1 calc R . . . .
H9B H -0.384306 -0.990931 -0.161743 0.264 Uiso 1 1 calc R . . . .
C10 C -0.4787(8) -0.9853(15) -0.1215(11) 0.235(7) Uani 1 1 d . . . . .
H10A H -0.447604 -0.920517 -0.067370 0.353 Uiso 1 1 calc GR . . . .
H10B H -0.477795 -1.093085 -0.100532 0.353 Uiso 1 1 calc GR . . . .
H10C H -0.535416 -0.948692 -0.146869 0.353 Uiso 1 1 calc GR . . . .
C11 C -0.3575(2) -0.4480(4) -0.2329(2) 0.0710(8) Uani 1 1 d . . . . .
C12 C -0.3322(3) -0.4031(6) -0.3079(3) 0.0880(11) Uani 1 1 d . . . . .
H12 H -0.361564 -0.439525 -0.370109 0.106 Uiso 1 1 calc R . . . .
C13 C -0.2644(4) -0.3054(8) -0.2940(6) 0.1223(19) Uani 1 1 d . . . . .
H13 H -0.248781 -0.275875 -0.346483 0.147 Uiso 1 1 calc R . . . .
C14 C -0.2206(3) -0.2527(8) -0.2042(7) 0.129(2) Uani 1 1 d . . . . .
H14 H -0.174332 -0.187835 -0.194401 0.155 Uiso 1 1 calc R . . . .
C15 C -0.2445(3) -0.2949(9) -0.1276(5) 0.130(2) Uani 1 1 d . . . . .
H15 H -0.213970 -0.258527 -0.065674 0.156 Uiso 1 1 calc R . . . .
C16 C -0.3141(3) -0.3920(8) -0.1409(4) 0.1075(16) Uani 1 1 d . . . . .
H16 H -0.330885 -0.418376 -0.088730 0.129 Uiso 1 1 calc R . . . .
C17 C -0.6763(2) -0.1840(6) -0.3079(3) 0.0881(11) Uani 1 1 d . . . . .
H17A H -0.652274 -0.103765 -0.337670 0.106 Uiso 1 1 calc R . . . .
H17B H -0.692739 -0.132822 -0.258035 0.106 Uiso 1 1 calc R . . . .
C18 C -0.7538(2) -0.2506(5) -0.3844(3) 0.0755(9) Uani 1 1 d . . . . .
C19 C -0.7939(2) -0.3807(6) -0.3655(3) 0.0890(11) Uani 1 1 d . . . . .
H19 H -0.771992 -0.432358 -0.306133 0.107 Uiso 1 1 calc R . . . .
C20 C -0.8667(3) -0.4355(7) -0.4341(4) 0.0995(13) Uani 1 1 d . . . . .
H20 H -0.893363 -0.523849 -0.420514 0.119 Uiso 1 1 calc R . . . .
C21 C -0.8998(2) -0.3619(7) -0.5213(3) 0.0957(13) Uani 1 1 d . . . . .
H21 H -0.949016 -0.399296 -0.566881 0.115 Uiso 1 1 calc R . . . .
C22 C -0.8607(3) -0.2330(7) -0.5415(3) 0.0938(13) Uani 1 1 d . . . . .
H22 H -0.882759 -0.182435 -0.601161 0.113 Uiso 1 1 calc R . . . .
C23 C -0.7878(2) -0.1774(6) -0.4728(3) 0.0857(11) Uani 1 1 d . . . . .
H23 H -0.761494 -0.089062 -0.486878 0.103 Uiso 1 1 calc R . . . .


_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
O1 C8 1.151(6) . ?
O2 C8 1.311(6) . ?
O2 C9 1.467(9) . ?
N1 C4 1.384(5) . ?
N1 C5 1.378(5) . ?
N1 C17 1.453(5) . ?
C1 H1 0.9800 . ?
C1 C2 1.512(5) . ?
C1 C8 1.521(6) . ?
C1 C11 1.521(5) . ?
C2 C3 1.412(5) . ?
C2 C5 1.369(5) . ?
C3 H3 0.9300 . ?
C3 C4 1.361(6) . ?
C4 C7 1.494(6) . ?
C5 C6 1.485(5) . ?
C6 H6A 0.9600 . ?
C6 H6B 0.9600 . ?
C6 H6C 0.9600 . ?
C7 H7A 0.9600 . ?
C7 H7B 0.9600 . ?
C7 H7C 0.9600 . ?
C9 H9A 0.9700 . ?
C9 H9B 0.9700 . ?
C9 C10 1.33(2) . ?
C10 H10A 0.9600 . ?
C10 H10B 0.9600 . ?
C10 H10C 0.9600 . ?
C11 C12 1.366(5) . ?
C11 C16 1.381(6) . ?
C12 H12 0.9300 . ?
C12 C13 1.377(8) . ?
C13 H13 0.9300 . ?
C13 C14 1.348(9) . ?
C14 H14 0.9300 . ?
C14 C15 1.367(10) . ?
C15 H15 0.9300 . ?
C15 C16 1.401(8) . ?
C16 H16 0.9300 . ?
C17 H17A 0.9700 . ?
C17 H17B 0.9700 . ?
C17 C18 1.517(5) . ?
C18 C19 1.373(6) . ?
C18 C23 1.374(6) . ?
C19 H19 0.9300 . ?
C19 C20 1.382(6) . ?
C20 H20 0.9300 . ?
C20 C21 1.358(7) . ?
C21 H21 0.9300 . ?
C21 C22 1.363(8) . ?
C22 H22 0.9300 . ?
C22 C23 1.384(6) . ?
C23 H23 0.9300 . ?

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
C8 O2 C9 116.1(5) . . ?
C4 N1 C17 126.0(3) . . ?
C5 N1 C4 109.3(3) . . ?
C5 N1 C17 124.7(3) . . ?
C2 C1 H1 107.1 . . ?
C2 C1 C8 111.8(3) . . ?
C2 C1 C11 112.0(3) . . ?
C8 C1 H1 107.1 . . ?
C8 C1 C11 111.4(3) . . ?
C11 C1 H1 107.1 . . ?
C3 C2 C1 127.8(3) . . ?
C5 C2 C1 124.8(3) . . ?
C5 C2 C3 107.2(3) . . ?
C2 C3 H3 125.7 . . ?
C4 C3 C2 108.7(3) . . ?
C4 C3 H3 125.7 . . ?
N1 C4 C7 123.0(4) . . ?
C3 C4 N1 107.0(3) . . ?
C3 C4 C7 129.9(4) . . ?
N1 C5 C6 122.6(3) . . ?
C2 C5 N1 107.8(3) . . ?
C2 C5 C6 129.6(4) . . ?
C5 C6 H6A 109.5 . . ?
C5 C6 H6B 109.5 . . ?
C5 C6 H6C 109.5 . . ?
H6A C6 H6B 109.5 . . ?
H6A C6 H6C 109.5 . . ?
H6B C6 H6C 109.5 . . ?
C4 C7 H7A 109.5 . . ?
C4 C7 H7B 109.5 . . ?
C4 C7 H7C 109.5 . . ?
H7A C7 H7B 109.5 . . ?
H7A C7 H7C 109.5 . . ?
H7B C7 H7C 109.5 . . ?
O1 C8 O2 123.1(5) . . ?
O1 C8 C1 125.5(5) . . ?
O2 C8 C1 111.3(3) . . ?
O2 C9 H9A 109.8 . . ?
O2 C9 H9B 109.8 . . ?
H9A C9 H9B 108.3 . . ?
C10 C9 O2 109.2(13) . . ?
C10 C9 H9A 109.8 . . ?
C10 C9 H9B 109.8 . . ?
C9 C10 H10A 109.5 . . ?
C9 C10 H10B 109.5 . . ?
C9 C10 H10C 109.5 . . ?
H10A C10 H10B 109.5 . . ?
H10A C10 H10C 109.5 . . ?
H10B C10 H10C 109.5 . . ?
C12 C11 C1 119.4(4) . . ?
C12 C11 C16 118.8(4) . . ?
C16 C11 C1 121.7(4) . . ?
C11 C12 H12 119.1 . . ?
C11 C12 C13 121.8(5) . . ?
C13 C12 H12 119.1 . . ?
C12 C13 H13 120.1 . . ?
C14 C13 C12 119.8(5) . . ?
C14 C13 H13 120.1 . . ?
C13 C14 H14 120.1 . . ?
C13 C14 C15 119.8(5) . . ?
C15 C14 H14 120.1 . . ?
C14 C15 H15 119.5 . . ?
C14 C15 C16 121.0(6) . . ?
C16 C15 H15 119.5 . . ?
C11 C16 C15 118.7(5) . . ?
C11 C16 H16 120.6 . . ?
C15 C16 H16 120.6 . . ?
N1 C17 H17A 108.7 . . ?
N1 C17 H17B 108.7 . . ?
N1 C17 C18 114.3(4) . . ?
H17A C17 H17B 107.6 . . ?
C18 C17 H17A 108.7 . . ?
C18 C17 H17B 108.7 . . ?
C19 C18 C17 121.0(4) . . ?
C19 C18 C23 118.2(4) . . ?
C23 C18 C17 120.7(4) . . ?
C18 C19 H19 119.8 . . ?
C18 C19 C20 120.4(4) . . ?
C20 C19 H19 119.8 . . ?
C19 C20 H20 119.6 . . ?
C21 C20 C19 120.8(5) . . ?
C21 C20 H20 119.6 . . ?
C20 C21 H21 120.2 . . ?
C20 C21 C22 119.7(4) . . ?
C22 C21 H21 120.2 . . ?
C21 C22 H22 120.1 . . ?
C21 C22 C23 119.8(4) . . ?
C23 C22 H22 120.1 . . ?
C18 C23 C22 121.2(4) . . ?
C18 C23 H23 119.4 . . ?
C22 C23 H23 119.4 . . ?

_olex2_submission_special_instructions 'No special instructions were received'
