# Electronic Supplementary Material (ESI) for Chemical Communications.
# This journal is © The Royal Society of Chemistry 2018

####################################################################### 
# 
# 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 
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data_sf20180619_lyn_0m
_database_code_depnum_ccdc_archive 'CCDC 1869247'
_audit_update_record             
;
2018-09-23 deposited with the CCDC.
2018-11-08 downloaded from the CCDC.
;
_audit_creation_date             2018-06-19
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.18 svn.r3508 for OlexSys, GUI svn.r5497)
;
_shelx_SHELXL_version_number     2017/1
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C18 H18 N2 O3 S'
_chemical_formula_sum            'C18 H18 N2 O3 S'
_chemical_formula_weight         342.40
_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 0.0033 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'
N N 0.0061 0.0033 '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'
S S 0.1246 0.1234 '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      orthorhombic
_space_group_IT_number           19
_space_group_name_H-M_alt        'P 21 21 21'
_space_group_name_Hall           'P 2ac 2ab'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, -y, z+1/2'
'-x, y+1/2, -z+1/2'
'x+1/2, -y+1/2, -z'

_cell_length_a                   8.2292(12)
_cell_length_b                   12.3415(18)
_cell_length_c                   17.181(3)
_cell_angle_alpha                90
_cell_angle_beta                 90
_cell_angle_gamma                90
_cell_volume                     1744.9(4)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    3885
_cell_measurement_temperature    296(2)
_cell_measurement_theta_max      25.669
_cell_measurement_theta_min      2.744
_shelx_estimated_absorpt_T_max   0.960
_shelx_estimated_absorpt_T_min   0.905
_exptl_absorpt_coefficient_mu    0.203
_exptl_absorpt_correction_T_max  0.7458
_exptl_absorpt_correction_T_min  0.6589
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
'SADABS-2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.0552 before and 0.0435 after correction. The Ratio of minimum to maximum transmission is 0.8835. The λ/2 correction factor is 0.0015.'
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            colourless
_exptl_crystal_density_diffrn    1.303
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             720
_exptl_crystal_size_max          0.5
_exptl_crystal_size_mid          0.3
_exptl_crystal_size_min          0.2
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0249
_diffrn_reflns_av_unetI/netI     0.0328
_diffrn_reflns_Laue_measured_fraction_full 0.998
_diffrn_reflns_Laue_measured_fraction_max 0.925
_diffrn_reflns_limit_h_max       10
_diffrn_reflns_limit_h_min       -8
_diffrn_reflns_limit_k_max       14
_diffrn_reflns_limit_k_min       -15
_diffrn_reflns_limit_l_max       22
_diffrn_reflns_limit_l_min       -22
_diffrn_reflns_number            10539
_diffrn_reflns_point_group_measured_fraction_full 0.998
_diffrn_reflns_point_group_measured_fraction_max 0.906
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         28.638
_diffrn_reflns_theta_min         2.744
_diffrn_ambient_temperature      296.15
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.998
_diffrn_measured_fraction_theta_max 0.925
_diffrn_measurement_device_type  'Bruker APEX-II CCD'
_diffrn_measurement_method       'φ and ω scans'
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   ?
_diffrn_standards_number         0
_reflns_Friedel_coverage         0.717
_reflns_Friedel_fraction_full    0.998
_reflns_Friedel_fraction_max     0.880
_reflns_number_gt                3579
_reflns_number_total             4058
_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 v7.68A (Bruker, 2009)'
_computing_data_collection       ?
_computing_data_reduction        'SAINT v7.68A (Bruker, 2009)'
_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         0.248
_refine_diff_density_min         -0.269
_refine_diff_density_rms         0.050
_refine_ls_abs_structure_details 
;
 Flack x determined using 1341 quotients [(I+)-(I-)]/[(I+)+(I-)]
 (Parsons, Flack and Wagner, Acta Cryst. B69 (2013) 249-259).
;
_refine_ls_abs_structure_Flack   0.00(3)
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.027
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     219
_refine_ls_number_reflns         4058
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.0472
_refine_ls_R_factor_gt           0.0403
_refine_ls_restrained_S_all      1.027
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0624P)²+0.0515P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.0981
_refine_ls_wR_factor_ref         0.1025
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups, All N(H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Ternary CH refined with riding coordinates:
 C1(H1A)
2.b Aromatic/amide H refined with riding coordinates:
 N1(H1), C4(H4), C6(H6), C7(H7), C9(H9), C13(H13), C14(H14), C16(H16), C17(H17)
2.c X=CH2 refined with riding coordinates:
 C10(H10A,H10B)
2.d Idealised Me refined as rotating group:
 C11(H11A,H11B,H11C), C18(H18A,H18B,H18C)
;
_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
S1 S 0.36618(8) 0.43910(5) 0.84159(3) 0.03733(17) Uani 1 1 d . . . . .
O1 O 0.5456(2) 0.23853(15) 0.82674(11) 0.0462(5) Uani 1 1 d . . . . .
O2 O 0.2817(3) 0.53340(15) 0.81289(11) 0.0482(5) Uani 1 1 d . . . . .
O3 O 0.4658(3) 0.45161(17) 0.90877(10) 0.0536(5) Uani 1 1 d . . . . .
N1 N 0.5966(3) 0.25703(17) 0.69800(12) 0.0431(6) Uani 1 1 d . . . . .
H1 H 0.652117 0.198016 0.697509 0.052 Uiso 1 1 calc R . . . .
N2 N 0.4718(3) 0.39618(16) 0.76491(11) 0.0345(5) Uani 1 1 d . . . . .
C1 C 0.5269(3) 0.47550(19) 0.70525(14) 0.0355(5) Uani 1 1 d . . . . .
H1A H 0.446624 0.534033 0.702322 0.043 Uiso 1 1 calc R . . . .
C2 C 0.5409(3) 0.2922(2) 0.76725(15) 0.0365(5) Uani 1 1 d . . . . .
C3 C 0.5705(4) 0.3099(2) 0.62601(15) 0.0430(6) Uani 1 1 d . . . . .
C4 C 0.5851(5) 0.2543(3) 0.55685(17) 0.0610(9) Uani 1 1 d . . . . .
H4 H 0.611797 0.181085 0.557103 0.073 Uiso 1 1 calc R . . . .
C5 C 0.5599(6) 0.3076(3) 0.48677(19) 0.0708(10) Uani 1 1 d . . . . .
C6 C 0.5210(5) 0.4169(3) 0.48809(18) 0.0670(10) Uani 1 1 d . . . . .
H6 H 0.504286 0.453528 0.441472 0.080 Uiso 1 1 calc R . . . .
C7 C 0.5068(4) 0.4721(3) 0.55768(16) 0.0515(7) Uani 1 1 d . . . . .
H7 H 0.480170 0.545322 0.557475 0.062 Uiso 1 1 calc R . . . .
C8 C 0.5319(3) 0.4191(2) 0.62795(15) 0.0385(6) Uani 1 1 d . . . . .
C9 C 0.6894(4) 0.5243(2) 0.72473(18) 0.0483(7) Uani 1 1 d . . . . .
H9 H 0.729414 0.575339 0.689786 0.058 Uiso 1 1 calc R . . . .
C10 C 0.7795(4) 0.5037(3) 0.7842(2) 0.0641(9) Uani 1 1 d . . . . .
H10A H 0.745666 0.453357 0.821090 0.077 Uiso 1 1 calc R . . . .
H10B H 0.878492 0.539098 0.790280 0.077 Uiso 1 1 calc R . . . .
C11 C 0.5737(9) 0.2462(4) 0.4099(2) 0.114(2) Uani 1 1 d . . . . .
H11A H 0.662648 0.196028 0.412673 0.171 Uiso 1 1 calc GR . . . .
H11B H 0.592407 0.296646 0.368289 0.171 Uiso 1 1 calc GR . . . .
H11C H 0.474666 0.207272 0.400286 0.171 Uiso 1 1 calc GR . . . .
C12 C 0.2242(3) 0.33551(19) 0.85742(14) 0.0356(5) Uani 1 1 d . . . . .
C13 C 0.2332(4) 0.2740(2) 0.92437(14) 0.0442(6) Uani 1 1 d . . . . .
H13 H 0.314073 0.286888 0.961012 0.053 Uiso 1 1 calc R . . . .
C14 C 0.1200(4) 0.1928(3) 0.93607(15) 0.0470(7) Uani 1 1 d . . . . .
H14 H 0.123987 0.151880 0.981485 0.056 Uiso 1 1 calc R . . . .
C15 C 0.0010(3) 0.1715(2) 0.88140(16) 0.0428(6) Uani 1 1 d . . . . .
C16 C -0.0054(4) 0.2353(3) 0.81501(17) 0.0485(7) Uani 1 1 d . . . . .
H16 H -0.085884 0.222481 0.778112 0.058 Uiso 1 1 calc R . . . .
C17 C 0.1051(3) 0.3172(2) 0.80279(15) 0.0442(6) Uani 1 1 d . . . . .
H17 H 0.099441 0.359648 0.758145 0.053 Uiso 1 1 calc R . . . .
C18 C -0.1161(5) 0.0803(3) 0.8920(2) 0.0656(9) Uani 1 1 d . . . . .
H18A H -0.224896 0.106393 0.884387 0.098 Uiso 1 1 calc GR . . . .
H18B H -0.105623 0.051539 0.943628 0.098 Uiso 1 1 calc GR . . . .
H18C H -0.093201 0.024456 0.854678 0.098 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
S1 O2 1.443(2) . ?
S1 O3 1.424(2) . ?
S1 N2 1.665(2) . ?
S1 C12 1.753(2) . ?
O1 C2 1.219(3) . ?
N1 H1 0.8600 . ?
N1 C2 1.347(3) . ?
N1 C3 1.415(3) . ?
N2 C1 1.488(3) . ?
N2 C2 1.404(3) . ?
C1 H1A 0.9800 . ?
C1 C8 1.500(3) . ?
C1 C9 1.505(4) . ?
C3 C4 1.377(4) . ?
C3 C8 1.386(4) . ?
C4 H4 0.9300 . ?
C4 C5 1.388(5) . ?
C5 C6 1.386(5) . ?
C5 C11 1.528(5) . ?
C6 H6 0.9300 . ?
C6 C7 1.381(4) . ?
C7 H7 0.9300 . ?
C7 C8 1.388(4) . ?
C9 H9 0.9300 . ?
C9 C10 1.288(4) . ?
C10 H10A 0.9300 . ?
C10 H10B 0.9300 . ?
C11 H11A 0.9600 . ?
C11 H11B 0.9600 . ?
C11 H11C 0.9600 . ?
C12 C13 1.380(3) . ?
C12 C17 1.375(4) . ?
C13 H13 0.9300 . ?
C13 C14 1.382(4) . ?
C14 H14 0.9300 . ?
C14 C15 1.382(4) . ?
C15 C16 1.387(4) . ?
C15 C18 1.492(4) . ?
C16 H16 0.9300 . ?
C16 C17 1.376(4) . ?
C17 H17 0.9300 . ?
C18 H18A 0.9600 . ?
C18 H18B 0.9600 . ?
C18 H18C 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
O2 S1 N2 103.77(11) . . ?
O2 S1 C12 108.66(13) . . ?
O3 S1 O2 117.84(13) . . ?
O3 S1 N2 112.04(13) . . ?
O3 S1 C12 109.70(12) . . ?
N2 S1 C12 103.81(11) . . ?
C2 N1 H1 117.5 . . ?
C2 N1 C3 124.9(2) . . ?
C3 N1 H1 117.5 . . ?
C1 N2 S1 119.65(16) . . ?
C2 N2 S1 118.66(17) . . ?
C2 N2 C1 119.8(2) . . ?
N2 C1 H1A 108.4 . . ?
N2 C1 C8 108.24(19) . . ?
N2 C1 C9 112.4(2) . . ?
C8 C1 H1A 108.4 . . ?
C8 C1 C9 111.0(2) . . ?
C9 C1 H1A 108.4 . . ?
O1 C2 N1 123.7(2) . . ?
O1 C2 N2 122.3(2) . . ?
N1 C2 N2 114.0(2) . . ?
C4 C3 N1 120.8(3) . . ?
C4 C3 C8 121.7(3) . . ?
C8 C3 N1 117.5(2) . . ?
C3 C4 H4 120.0 . . ?
C3 C4 C5 120.0(3) . . ?
C5 C4 H4 120.0 . . ?
C4 C5 C11 120.2(4) . . ?
C6 C5 C4 118.8(3) . . ?
C6 C5 C11 120.9(3) . . ?
C5 C6 H6 119.5 . . ?
C7 C6 C5 120.9(3) . . ?
C7 C6 H6 119.5 . . ?
C6 C7 H7 119.7 . . ?
C6 C7 C8 120.5(3) . . ?
C8 C7 H7 119.7 . . ?
C3 C8 C1 118.6(2) . . ?
C3 C8 C7 118.1(3) . . ?
C7 C8 C1 123.2(2) . . ?
C1 C9 H9 116.2 . . ?
C10 C9 C1 127.5(3) . . ?
C10 C9 H9 116.2 . . ?
C9 C10 H10A 120.0 . . ?
C9 C10 H10B 120.0 . . ?
H10A C10 H10B 120.0 . . ?
C5 C11 H11A 109.5 . . ?
C5 C11 H11B 109.5 . . ?
C5 C11 H11C 109.5 . . ?
H11A C11 H11B 109.5 . . ?
H11A C11 H11C 109.5 . . ?
H11B C11 H11C 109.5 . . ?
C13 C12 S1 119.6(2) . . ?
C17 C12 S1 119.25(19) . . ?
C17 C12 C13 121.1(2) . . ?
C12 C13 H13 120.5 . . ?
C12 C13 C14 118.9(3) . . ?
C14 C13 H13 120.5 . . ?
C13 C14 H14 119.5 . . ?
C15 C14 C13 121.1(2) . . ?
C15 C14 H14 119.5 . . ?
C14 C15 C16 118.5(2) . . ?
C14 C15 C18 121.2(3) . . ?
C16 C15 C18 120.2(3) . . ?
C15 C16 H16 119.4 . . ?
C17 C16 C15 121.1(3) . . ?
C17 C16 H16 119.4 . . ?
C12 C17 C16 119.2(2) . . ?
C12 C17 H17 120.4 . . ?
C16 C17 H17 120.4 . . ?
C15 C18 H18A 109.5 . . ?
C15 C18 H18B 109.5 . . ?
C15 C18 H18C 109.5 . . ?
H18A C18 H18B 109.5 . . ?
H18A C18 H18C 109.5 . . ?
H18B C18 H18C 109.5 . . ?

_olex2_submission_special_instructions 'No special instructions were received'
