Literature DB >> 22347100

Ethyl (2R,3S)-2-benzoyl-3-(4-bromo-phen-yl)-4-nitro-butano-ate.

Yifeng Wang, Ke Wang, Zhaobo Li, Danqian Xu.   

Abstract

The title compoud, C(19)H(18)BrNO(5), was synthesized by an organocatalytic reaction. The aymmetric unit contains two independent mol-ecules, in each of which the carbon between the two carbonyl groups adopts an R configuration, while the adjacent C atom has an S configuration. The dihedral angle between the two benzene rings is different in the two mol-ecules [11.64 (3) and 58.96 (4)°].

Entities:  

Year:  2012        PMID: 22347100      PMCID: PMC3275244          DOI: 10.1107/S1600536812002073

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For the asymmetric synthesis of the title compound, see: Bae et al. (2011 ▶); Malerich et al. (2008 ▶).

Experimental

Crystal data

C19H18BrNO5 M = 420.25 Monoclinic, a = 5.7558 (3) Å b = 21.6262 (9) Å c = 15.1337 (7) Å β = 93.720 (1)° V = 1879.81 (15) Å3 Z = 4 Mo Kα radiation μ = 2.22 mm−1 T = 296 K 0.48 × 0.30 × 0.27 mm

Data collection

Rigaku R-AXIS RAPID/ZJUG diffractometer Absorption correction: multi-scan (ABSCOR; Higashi, 1995 ▶) T min = 0.346, T max = 0.549 16125 measured reflections 7326 independent reflections 4316 reflections with I > 2σ(I) R int = 0.043

Refinement

R[F 2 > 2σ(F 2)] = 0.046 wR(F 2) = 0.127 S = 1.00 7326 reflections 469 parameters 27 restraints H-atom parameters constrained Δρmax = 0.42 e Å−3 Δρmin = −0.54 e Å−3 Absolute structure: Flack (1983 ▶), 3541 Friedel pairs Flack parameter: −0.013 (9) Data collection: PROCESS-AUTO (Rigaku, 2007 ▶); cell refinement: PROCESS-AUTO; data reduction: CrystalClear (Rigaku, 2007 ▶); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997 ▶); software used to prepare material for publication: WinGX (Farrugia, 1999 ▶). Crystal structure: contains datablock(s) global, I. DOI: 10.1107/S1600536812002073/bt5738sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536812002073/bt5738Isup2.hkl Supplementary material file. DOI: 10.1107/S1600536812002073/bt5738Isup3.cml Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C19H18BrNO5F(000) = 856
Mr = 420.25Dx = 1.485 Mg m3
Monoclinic, P21Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ybCell parameters from 11156 reflections
a = 5.7558 (3) Åθ = 3.1–27.4°
b = 21.6262 (9) ŵ = 2.22 mm1
c = 15.1337 (7) ÅT = 296 K
β = 93.720 (1)°Needle, colorless
V = 1879.81 (15) Å30.48 × 0.30 × 0.27 mm
Z = 4
Rigaku R-AXIS RAPID/ZJUG diffractometer7326 independent reflections
Radiation source: rotating anode4316 reflections with I > 2σ(I)
graphiteRint = 0.043
Detector resolution: 10.00 pixels mm-1θmax = 26.0°, θmin = 3.1°
ω scansh = −7→6
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)k = −26→26
Tmin = 0.346, Tmax = 0.549l = −18→18
16125 measured reflections
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.046H-atom parameters constrained
wR(F2) = 0.127w = 1/[σ2(Fo2) + (0.0512P)2 + 0.3123P] where P = (Fo2 + 2Fc2)/3
S = 1.00(Δ/σ)max = 0.001
7326 reflectionsΔρmax = 0.42 e Å3
469 parametersΔρmin = −0.54 e Å3
27 restraintsAbsolute structure: Flack (1983), 3541 Friedel pairs
Primary atom site location: structure-invariant direct methodsFlack parameter: −0.013 (9)
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
Refinement. 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 > σ(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.
xyzUiso*/Ueq
Br1A1.29441 (11)0.56418 (3)0.17401 (5)0.0918 (3)
O1A0.4552 (6)0.81610 (17)0.4794 (3)0.0671 (11)
O2A0.6040 (7)0.7964 (2)0.2713 (3)0.0736 (11)
O3A0.9340 (7)0.85124 (18)0.2842 (2)0.0662 (10)
O4A0.6867 (9)0.6324 (2)0.5360 (3)0.0795 (12)
O5A1.0065 (11)0.6395 (2)0.6147 (4)0.1024 (17)
N1A0.8595 (10)0.6601 (2)0.5607 (3)0.0626 (12)
C1A0.7975 (8)0.7339 (2)0.4326 (3)0.0424 (11)
H1A0.63210.72270.42880.051*
C2A0.8168 (8)0.8036 (2)0.4127 (3)0.0403 (10)
H2A0.97400.81790.43120.048*
C3A0.6384 (9)0.8405 (2)0.4625 (3)0.0476 (12)
C4A0.6864 (9)0.9065 (2)0.4869 (3)0.0466 (12)
C5A0.5307 (10)0.9361 (3)0.5379 (4)0.0645 (15)
H5A0.40350.91450.55700.077*
C6A0.5620 (12)0.9975 (3)0.5609 (5)0.0782 (19)
H6A0.45381.01780.59360.094*
C7A0.7557 (11)1.0283 (3)0.5348 (4)0.0710 (17)
H7A0.78011.06930.55140.085*
C8A0.9117 (11)0.9994 (3)0.4848 (4)0.0668 (17)
H8A1.03871.02140.46620.080*
C9A0.8838 (9)0.9384 (2)0.4617 (4)0.0568 (14)
H9A0.99430.91850.42970.068*
C10A0.7691 (9)0.8160 (2)0.3148 (4)0.0472 (12)
C11A0.9041 (14)0.8701 (4)0.1943 (5)0.101 (2)
H11A0.86190.91350.19160.121*
H11B0.77820.84660.16470.121*
C12A1.1267 (16)0.8601 (6)0.1466 (8)0.160 (4)
H12A1.10160.87280.08590.240*
H12B1.16820.81710.14900.240*
H12C1.25040.88420.17490.240*
C13A0.8929 (10)0.7242 (2)0.5278 (3)0.0533 (13)
H13A1.05790.73380.53190.064*
H13B0.81670.75290.56580.064*
C14A0.9208 (8)0.6937 (2)0.3675 (3)0.0428 (11)
C15A0.8224 (8)0.6384 (2)0.3383 (3)0.0460 (12)
H15A0.67960.62670.35850.055*
C16A0.9288 (9)0.5998 (3)0.2802 (4)0.0587 (14)
H16A0.85890.56270.26230.070*
C17A1.1408 (8)0.6170 (3)0.2490 (4)0.0524 (13)
C18A1.2407 (9)0.6726 (3)0.2778 (4)0.0575 (14)
H18A1.38300.68440.25740.069*
C19A1.1330 (8)0.7107 (2)0.3363 (3)0.0485 (12)
H19A1.20300.74760.35470.058*
Br1B0.63666 (15)0.41912 (3)1.11381 (5)0.0991 (3)
O1B0.5085 (6)0.70722 (17)0.6957 (2)0.0607 (10)
O2B0.1843 (7)0.6699 (2)0.9555 (3)0.0829 (13)
O3B0.5254 (7)0.7107 (2)0.9220 (2)0.0708 (11)
O4B0.8589 (9)0.5332 (2)0.7336 (4)0.0899 (15)
O5B0.6010 (12)0.4713 (3)0.6777 (5)0.147 (3)
N1B0.6594 (11)0.5201 (3)0.7085 (3)0.0722 (14)
C1B0.5169 (8)0.6042 (2)0.8032 (3)0.0474 (12)
H1B0.66660.62550.80070.057*
C2B0.3228 (8)0.6546 (2)0.8097 (3)0.0450 (11)
H2B0.17090.63510.79620.054*
C3B0.3503 (8)0.7079 (2)0.7448 (3)0.0468 (12)
C4B0.1843 (9)0.7606 (2)0.7434 (3)0.0498 (12)
C5B0.2286 (10)0.8121 (3)0.6921 (4)0.0553 (14)
H5B0.35890.81280.65880.066*
C6B0.0800 (11)0.8622 (3)0.6902 (4)0.0674 (16)
H6B0.11220.89670.65630.081*
C7B−0.1159 (10)0.8617 (3)0.7381 (4)0.0611 (15)
H7B−0.21710.89530.73560.073*
C8B−0.1600 (10)0.8112 (3)0.7895 (4)0.0667 (16)
H8B−0.28990.81100.82300.080*
C9B−0.0138 (9)0.7608 (3)0.7918 (4)0.0569 (14)
H9B−0.04750.72660.82590.068*
C10B0.3312 (10)0.6787 (3)0.9041 (4)0.0555 (13)
C11B0.5567 (14)0.7394 (4)1.0100 (5)0.105 (2)
H11C0.40560.74791.03220.126*
H11D0.63850.77841.00550.126*
C12B0.6951 (17)0.6968 (4)1.0744 (6)0.133 (3)
H12D0.71240.71601.13160.199*
H12E0.84600.68921.05310.199*
H12F0.61380.65821.07890.199*
C13B0.4719 (8)0.5678 (3)0.7169 (3)0.0565 (13)
H13C0.32130.54770.71660.068*
H13D0.46970.59590.66690.068*
C14B0.5342 (7)0.5612 (3)0.8821 (3)0.0459 (11)
C15B0.7338 (8)0.5612 (3)0.9380 (4)0.0590 (13)
H15B0.85110.58960.92870.071*
C16B0.7630 (10)0.5195 (3)1.0080 (4)0.0648 (16)
H16B0.89840.52001.04500.078*
C17B0.5928 (10)0.4783 (3)1.0216 (4)0.0612 (15)
C18B0.3873 (10)0.4772 (3)0.9684 (4)0.0584 (14)
H18B0.26990.44920.97920.070*
C19B0.3612 (9)0.5190 (3)0.8987 (4)0.0546 (13)
H19B0.22460.51860.86240.066*
U11U22U33U12U13U23
Br1A0.0684 (4)0.1068 (6)0.1006 (5)0.0089 (4)0.0095 (4)−0.0550 (5)
O1A0.058 (2)0.051 (2)0.095 (3)−0.0120 (19)0.029 (2)−0.011 (2)
O2A0.077 (3)0.080 (3)0.061 (3)−0.012 (2)−0.016 (2)0.010 (2)
O3A0.078 (3)0.069 (3)0.052 (2)−0.009 (2)0.0129 (19)0.020 (2)
O4A0.110 (3)0.067 (3)0.062 (3)−0.026 (3)0.016 (3)0.007 (2)
O5A0.144 (4)0.063 (3)0.096 (4)0.020 (3)−0.031 (3)0.020 (3)
N1A0.095 (4)0.043 (3)0.051 (3)−0.006 (3)0.005 (3)−0.001 (2)
C1A0.052 (3)0.033 (3)0.042 (3)−0.004 (2)0.000 (2)0.000 (2)
C2A0.041 (2)0.037 (3)0.043 (3)0.000 (2)0.002 (2)0.000 (2)
C3A0.053 (3)0.038 (3)0.052 (3)−0.003 (2)0.007 (3)−0.004 (2)
C4A0.057 (3)0.036 (3)0.045 (3)0.003 (2)−0.006 (2)−0.002 (2)
C5A0.063 (3)0.052 (4)0.081 (4)0.007 (3)0.017 (3)−0.004 (3)
C6A0.088 (4)0.054 (4)0.094 (5)0.003 (3)0.019 (4)−0.022 (4)
C7A0.085 (4)0.042 (3)0.084 (5)−0.003 (3)−0.006 (4)−0.008 (3)
C8A0.073 (4)0.042 (3)0.085 (5)−0.015 (3)0.008 (4)−0.001 (3)
C9A0.055 (3)0.041 (3)0.074 (4)−0.005 (2)0.004 (3)−0.006 (3)
C10A0.054 (3)0.036 (3)0.052 (3)0.001 (2)0.006 (3)0.004 (2)
C11A0.101 (3)0.102 (3)0.100 (3)−0.0004 (10)0.0069 (10)0.0018 (10)
C12A0.159 (4)0.161 (4)0.159 (4)0.0003 (10)0.0108 (11)0.0007 (10)
C13A0.075 (3)0.036 (3)0.049 (3)−0.006 (2)0.001 (3)−0.004 (2)
C14A0.045 (2)0.039 (3)0.043 (3)0.006 (2)−0.005 (2)−0.002 (2)
C15A0.042 (3)0.040 (3)0.056 (3)−0.005 (2)0.002 (2)−0.008 (2)
C16A0.052 (3)0.052 (3)0.071 (4)0.000 (3)−0.005 (3)−0.019 (3)
C17A0.049 (3)0.056 (3)0.050 (3)0.009 (3)−0.005 (2)−0.005 (3)
C18A0.044 (3)0.062 (4)0.066 (4)−0.001 (3)0.000 (3)−0.008 (3)
C19A0.044 (3)0.046 (3)0.056 (3)−0.003 (2)0.009 (2)−0.006 (2)
Br1B0.1217 (6)0.0991 (6)0.0771 (5)0.0286 (5)0.0117 (4)0.0363 (4)
O1B0.065 (2)0.054 (2)0.065 (2)0.0025 (18)0.022 (2)0.0053 (19)
O2B0.081 (3)0.100 (3)0.072 (3)0.003 (3)0.035 (2)0.002 (2)
O3B0.087 (3)0.080 (3)0.044 (2)−0.019 (2)0.0017 (19)−0.015 (2)
O4B0.067 (3)0.109 (4)0.096 (4)0.022 (3)0.020 (3)0.006 (3)
O5B0.160 (5)0.103 (5)0.167 (6)0.050 (4)−0.062 (5)−0.078 (5)
N1B0.094 (4)0.070 (4)0.052 (3)0.025 (3)−0.002 (3)0.000 (3)
C1B0.045 (3)0.049 (3)0.048 (3)−0.004 (2)0.004 (2)−0.003 (2)
C2B0.046 (3)0.045 (3)0.044 (3)−0.005 (2)0.007 (2)0.002 (2)
C3B0.046 (3)0.044 (3)0.051 (3)−0.003 (2)0.008 (2)0.001 (2)
C4B0.049 (3)0.050 (3)0.050 (3)−0.002 (2)0.003 (2)−0.005 (3)
C5B0.060 (3)0.058 (4)0.049 (3)0.007 (3)0.007 (3)0.009 (3)
C6B0.076 (4)0.066 (4)0.059 (4)0.001 (3)−0.008 (3)0.004 (3)
C7B0.059 (3)0.052 (4)0.073 (4)0.006 (3)0.003 (3)0.000 (3)
C8B0.058 (3)0.061 (4)0.083 (4)−0.002 (3)0.012 (3)−0.002 (3)
C9B0.051 (3)0.056 (4)0.065 (4)−0.001 (3)0.007 (3)0.002 (3)
C10B0.060 (3)0.055 (3)0.052 (3)0.004 (3)0.009 (3)0.005 (3)
C11B0.105 (3)0.105 (3)0.104 (3)−0.0009 (10)0.0065 (10)−0.0009 (10)
C12B0.133 (3)0.133 (3)0.132 (3)−0.0001 (10)0.0087 (10)−0.0007 (10)
C13B0.061 (3)0.059 (3)0.050 (3)0.009 (3)0.003 (2)−0.004 (3)
C14B0.039 (2)0.050 (3)0.047 (3)−0.002 (3)−0.002 (2)0.001 (3)
C15B0.048 (3)0.070 (4)0.059 (3)−0.011 (3)−0.002 (3)0.005 (3)
C16B0.053 (3)0.085 (5)0.054 (4)0.010 (3)−0.013 (3)0.011 (3)
C17B0.067 (4)0.064 (4)0.052 (3)0.015 (3)0.007 (3)−0.009 (3)
C18B0.067 (3)0.050 (3)0.059 (4)−0.011 (3)0.009 (3)0.004 (3)
C19B0.051 (3)0.061 (3)0.050 (3)−0.004 (3)−0.005 (2)0.006 (3)
Br1A—C17A1.872 (5)Br1B—C17B1.899 (6)
O1A—C3A1.221 (6)O1B—C3B1.212 (5)
O2A—C10A1.197 (6)O2B—C10B1.201 (6)
O3A—C10A1.324 (6)O3B—C10B1.328 (7)
O3A—C11A1.420 (9)O3B—C11B1.470 (9)
O4A—N1A1.201 (6)O4B—N1B1.219 (7)
O5A—N1A1.222 (6)O5B—N1B1.193 (7)
N1A—C13A1.490 (7)N1B—C13B1.505 (7)
C1A—C13A1.522 (7)C1B—C14B1.510 (7)
C1A—C14A1.524 (6)C1B—C13B1.533 (7)
C1A—C2A1.542 (6)C1B—C2B1.568 (7)
C1A—H1A0.9800C1B—H1B0.9800
C2A—C10A1.513 (7)C2B—C10B1.518 (7)
C2A—C3A1.536 (7)C2B—C3B1.530 (7)
C2A—H2A0.9800C2B—H2B0.9800
C3A—C4A1.497 (7)C3B—C4B1.486 (7)
C4A—C5A1.377 (7)C4B—C5B1.392 (7)
C4A—C9A1.403 (7)C4B—C9B1.395 (7)
C5A—C6A1.382 (8)C5B—C6B1.380 (8)
C5A—H5A0.9300C5B—H5B0.9300
C6A—C7A1.379 (9)C6B—C7B1.379 (8)
C6A—H6A0.9300C6B—H6B0.9300
C7A—C8A1.363 (8)C7B—C8B1.375 (8)
C7A—H7A0.9300C7B—H7B0.9300
C8A—C9A1.371 (7)C8B—C9B1.376 (8)
C8A—H8A0.9300C8B—H8B0.9300
C9A—H9A0.9300C9B—H9B0.9300
C11A—C12A1.527 (3)C11B—C12B1.528 (3)
C11A—H11A0.9700C11B—H11C0.9700
C11A—H11B0.9700C11B—H11D0.9700
C12A—H12A0.9600C12B—H12D0.9600
C12A—H12B0.9600C12B—H12E0.9600
C12A—H12C0.9600C12B—H12F0.9600
C13A—H13A0.9700C13B—H13C0.9700
C13A—H13B0.9700C13B—H13D0.9700
C14A—C15A1.384 (7)C14B—C15B1.382 (7)
C14A—C19A1.387 (7)C14B—C19B1.386 (7)
C15A—C16A1.382 (7)C15B—C16B1.393 (8)
C15A—H15A0.9300C15B—H15B0.9300
C16A—C17A1.387 (7)C16B—C17B1.349 (8)
C16A—H16A0.9300C16B—H16B0.9300
C17A—C18A1.389 (7)C17B—C18B1.387 (8)
C18A—C19A1.385 (7)C18B—C19B1.390 (7)
C18A—H18A0.9300C18B—H18B0.9300
C19A—H19A0.9300C19B—H19B0.9300
C10A—O3A—C11A117.1 (5)C10B—O3B—C11B117.2 (5)
O4A—N1A—O5A123.3 (5)O5B—N1B—O4B124.2 (6)
O4A—N1A—C13A118.9 (5)O5B—N1B—C13B117.1 (6)
O5A—N1A—C13A117.7 (5)O4B—N1B—C13B118.7 (6)
C13A—C1A—C14A112.3 (4)C14B—C1B—C13B110.9 (4)
C13A—C1A—C2A107.1 (4)C14B—C1B—C2B112.9 (4)
C14A—C1A—C2A112.8 (4)C13B—C1B—C2B109.1 (4)
C13A—C1A—H1A108.2C14B—C1B—H1B107.9
C14A—C1A—H1A108.2C13B—C1B—H1B107.9
C2A—C1A—H1A108.2C2B—C1B—H1B107.9
C10A—C2A—C3A107.6 (4)C10B—C2B—C3B110.3 (4)
C10A—C2A—C1A110.8 (4)C10B—C2B—C1B108.5 (4)
C3A—C2A—C1A110.7 (4)C3B—C2B—C1B112.3 (4)
C10A—C2A—H2A109.2C10B—C2B—H2B108.5
C3A—C2A—H2A109.2C3B—C2B—H2B108.5
C1A—C2A—H2A109.2C1B—C2B—H2B108.5
O1A—C3A—C4A120.5 (5)O1B—C3B—C4B120.6 (4)
O1A—C3A—C2A119.5 (4)O1B—C3B—C2B119.9 (4)
C4A—C3A—C2A119.9 (4)C4B—C3B—C2B119.6 (4)
C5A—C4A—C9A119.5 (5)C5B—C4B—C9B118.4 (5)
C5A—C4A—C3A117.7 (5)C5B—C4B—C3B118.7 (4)
C9A—C4A—C3A122.8 (5)C9B—C4B—C3B122.8 (5)
C4A—C5A—C6A120.6 (6)C6B—C5B—C4B120.3 (5)
C4A—C5A—H5A119.7C6B—C5B—H5B119.8
C6A—C5A—H5A119.7C4B—C5B—H5B119.8
C7A—C6A—C5A119.1 (6)C7B—C6B—C5B120.7 (6)
C7A—C6A—H6A120.4C7B—C6B—H6B119.7
C5A—C6A—H6A120.4C5B—C6B—H6B119.7
C8A—C7A—C6A120.8 (6)C6B—C7B—C8B119.4 (5)
C8A—C7A—H7A119.6C6B—C7B—H7B120.3
C6A—C7A—H7A119.6C8B—C7B—H7B120.3
C7A—C8A—C9A120.8 (6)C9B—C8B—C7B120.6 (5)
C7A—C8A—H8A119.6C9B—C8B—H8B119.7
C9A—C8A—H8A119.6C7B—C8B—H8B119.7
C8A—C9A—C4A119.2 (5)C8B—C9B—C4B120.6 (5)
C8A—C9A—H9A120.4C8B—C9B—H9B119.7
C4A—C9A—H9A120.4C4B—C9B—H9B119.7
O2A—C10A—O3A124.9 (5)O2B—C10B—O3B124.7 (5)
O2A—C10A—C2A124.2 (5)O2B—C10B—C2B125.0 (5)
O3A—C10A—C2A110.9 (4)O3B—C10B—C2B110.3 (4)
O3A—C11A—C12A111.1 (7)O3B—C11B—C12B110.5 (7)
O3A—C11A—H11A109.4O3B—C11B—H11C109.5
C12A—C11A—H11A109.4C12B—C11B—H11C109.5
O3A—C11A—H11B109.4O3B—C11B—H11D109.5
C12A—C11A—H11B109.4C12B—C11B—H11D109.5
H11A—C11A—H11B108.0H11C—C11B—H11D108.1
C11A—C12A—H12A109.5C11B—C12B—H12D109.5
C11A—C12A—H12B109.5C11B—C12B—H12E109.5
H12A—C12A—H12B109.5H12D—C12B—H12E109.5
C11A—C12A—H12C109.5C11B—C12B—H12F109.5
H12A—C12A—H12C109.5H12D—C12B—H12F109.5
H12B—C12A—H12C109.5H12E—C12B—H12F109.5
N1A—C13A—C1A113.5 (4)N1B—C13B—C1B110.0 (4)
N1A—C13A—H13A108.9N1B—C13B—H13C109.7
C1A—C13A—H13A108.9C1B—C13B—H13C109.7
N1A—C13A—H13B108.9N1B—C13B—H13D109.7
C1A—C13A—H13B108.9C1B—C13B—H13D109.7
H13A—C13A—H13B107.7H13C—C13B—H13D108.2
C15A—C14A—C19A118.1 (4)C15B—C14B—C19B117.8 (5)
C15A—C14A—C1A120.1 (4)C15B—C14B—C1B119.6 (4)
C19A—C14A—C1A121.8 (4)C19B—C14B—C1B122.5 (4)
C16A—C15A—C14A122.3 (5)C14B—C15B—C16B121.4 (5)
C16A—C15A—H15A118.8C14B—C15B—H15B119.3
C14A—C15A—H15A118.8C16B—C15B—H15B119.3
C15A—C16A—C17A119.4 (5)C17B—C16B—C15B119.3 (5)
C15A—C16A—H16A120.3C17B—C16B—H16B120.3
C17A—C16A—H16A120.3C15B—C16B—H16B120.3
C16A—C17A—C18A118.7 (5)C16B—C17B—C18B121.6 (5)
C16A—C17A—Br1A120.2 (4)C16B—C17B—Br1B119.6 (4)
C18A—C17A—Br1A121.0 (4)C18B—C17B—Br1B118.8 (5)
C19A—C18A—C17A121.4 (5)C17B—C18B—C19B118.3 (5)
C19A—C18A—H18A119.3C17B—C18B—H18B120.8
C17A—C18A—H18A119.3C19B—C18B—H18B120.8
C18A—C19A—C14A120.1 (5)C14B—C19B—C18B121.5 (5)
C18A—C19A—H19A120.0C14B—C19B—H19B119.2
C14A—C19A—H19A120.0C18B—C19B—H19B119.2
C13A—C1A—C2A—C10A169.2 (4)C14B—C1B—C2B—C10B41.7 (5)
C14A—C1A—C2A—C10A45.2 (5)C13B—C1B—C2B—C10B165.5 (4)
C13A—C1A—C2A—C3A−71.5 (5)C14B—C1B—C2B—C3B164.0 (4)
C14A—C1A—C2A—C3A164.5 (4)C13B—C1B—C2B—C3B−72.2 (5)
C10A—C2A—C3A—O1A92.0 (6)C10B—C2B—C3B—O1B121.8 (5)
C1A—C2A—C3A—O1A−29.2 (7)C1B—C2B—C3B—O1B0.6 (7)
C10A—C2A—C3A—C4A−85.8 (6)C10B—C2B—C3B—C4B−57.3 (6)
C1A—C2A—C3A—C4A153.0 (4)C1B—C2B—C3B—C4B−178.5 (4)
O1A—C3A—C4A—C5A7.5 (8)O1B—C3B—C4B—C5B−7.0 (7)
C2A—C3A—C4A—C5A−174.6 (5)C2B—C3B—C4B—C5B172.1 (5)
O1A—C3A—C4A—C9A−173.9 (5)O1B—C3B—C4B—C9B173.3 (5)
C2A—C3A—C4A—C9A3.9 (8)C2B—C3B—C4B—C9B−7.6 (7)
C9A—C4A—C5A—C6A2.9 (9)C9B—C4B—C5B—C6B0.6 (8)
C3A—C4A—C5A—C6A−178.4 (6)C3B—C4B—C5B—C6B−179.1 (5)
C4A—C5A—C6A—C7A−2.3 (10)C4B—C5B—C6B—C7B−0.9 (9)
C5A—C6A—C7A—C8A1.8 (10)C5B—C6B—C7B—C8B1.3 (9)
C6A—C7A—C8A—C9A−2.1 (10)C6B—C7B—C8B—C9B−1.5 (9)
C7A—C8A—C9A—C4A2.8 (9)C7B—C8B—C9B—C4B1.3 (9)
C5A—C4A—C9A—C8A−3.2 (9)C5B—C4B—C9B—C8B−0.9 (8)
C3A—C4A—C9A—C8A178.3 (5)C3B—C4B—C9B—C8B178.9 (5)
C11A—O3A—C10A—O2A4.1 (8)C11B—O3B—C10B—O2B−2.7 (8)
C11A—O3A—C10A—C2A−176.0 (5)C11B—O3B—C10B—C2B177.7 (5)
C3A—C2A—C10A—O2A−71.6 (6)C3B—C2B—C10B—O2B125.2 (6)
C1A—C2A—C10A—O2A49.5 (7)C1B—C2B—C10B—O2B−111.3 (6)
C3A—C2A—C10A—O3A108.4 (5)C3B—C2B—C10B—O3B−55.2 (6)
C1A—C2A—C10A—O3A−130.5 (4)C1B—C2B—C10B—O3B68.3 (5)
C10A—O3A—C11A—C12A−132.7 (7)C10B—O3B—C11B—C12B93.6 (7)
O4A—N1A—C13A—C1A−34.8 (7)O5B—N1B—C13B—C1B141.9 (6)
O5A—N1A—C13A—C1A148.1 (5)O4B—N1B—C13B—C1B−37.6 (7)
C14A—C1A—C13A—N1A−62.7 (6)C14B—C1B—C13B—N1B−56.3 (5)
C2A—C1A—C13A—N1A173.0 (4)C2B—C1B—C13B—N1B178.8 (4)
C13A—C1A—C14A—C15A97.8 (5)C13B—C1B—C14B—C15B122.3 (5)
C2A—C1A—C14A—C15A−141.2 (5)C2B—C1B—C14B—C15B−114.9 (5)
C13A—C1A—C14A—C19A−81.7 (6)C13B—C1B—C14B—C19B−54.4 (6)
C2A—C1A—C14A—C19A39.4 (6)C2B—C1B—C14B—C19B68.4 (6)
C19A—C14A—C15A—C16A0.4 (7)C19B—C14B—C15B—C16B1.1 (8)
C1A—C14A—C15A—C16A−179.0 (5)C1B—C14B—C15B—C16B−175.7 (5)
C14A—C15A—C16A—C17A−0.6 (8)C14B—C15B—C16B—C17B−0.1 (9)
C15A—C16A—C17A—C18A0.5 (8)C15B—C16B—C17B—C18B−1.1 (9)
C15A—C16A—C17A—Br1A177.5 (4)C15B—C16B—C17B—Br1B177.4 (4)
C16A—C17A—C18A—C19A−0.2 (8)C16B—C17B—C18B—C19B1.3 (8)
Br1A—C17A—C18A—C19A−177.2 (4)Br1B—C17B—C18B—C19B−177.2 (4)
C17A—C18A—C19A—C14A0.0 (8)C15B—C14B—C19B—C18B−0.9 (8)
C15A—C14A—C19A—C18A−0.2 (7)C1B—C14B—C19B—C18B175.8 (5)
C1A—C14A—C19A—C18A179.3 (5)C17B—C18B—C19B—C14B−0.3 (8)
  3 in total

1.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

2.  Hydrogen bonding mediated enantioselective organocatalysis in brine: significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to β-nitroolefins.

Authors:  Han Yong Bae; Surajit Some; Joong Suk Oh; Yong Seop Lee; Choong Eui Song
Journal:  Chem Commun (Camb)       Date:  2011-07-25       Impact factor: 6.222

3.  Chiral squaramide derivatives are excellent hydrogen bond donor catalysts.

Authors:  Jeremiah P Malerich; Koji Hagihara; Viresh H Rawal
Journal:  J Am Chem Soc       Date:  2008-10-11       Impact factor: 15.419

  3 in total

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