Literature DB >> 21583566

Benzyl 3-dehydr-oxy-1,2,5-oxadiazolo[3',4':2,3]oleanolate.

Jun Hu1, Xiaoyun Gong, Ruji Wang, Yong Ju.   

Abstract

The title compound, C(37)H(50)N(2)O(3), is a benzyl ester derivative of oleanolic acid, a penta-cyclic triterpene, with a five-membered oxadiazole ring fused to the ring A. The triterpene A and C rings adopt slightly distorted half-chair conformations, whereas the remaining three six-membered rings are in chair forms.

Entities:  

Year:  2009        PMID: 21583566      PMCID: PMC2977140          DOI: 10.1107/S1600536809026695

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


Related literature

For information on oleanolic acid and its derivatives, see: Chen et al. (2006 ▶); Liu (2005 ▶).

Experimental

Crystal data

C37H50N2O3 M = 570.79 Orthorhombic, a = 8.7124 (19) Å b = 19.054 (3) Å c = 19.480 (3) Å V = 3233.7 (10) Å3 Z = 4 Mo Kα radiation μ = 0.07 mm−1 T = 295 K 0.4 × 0.3 × 0.2 mm

Data collection

Bruker P4 diffractometer Absorption correction: none 4315 measured reflections 3398 independent reflections 1649 reflections with I > 2σ(I) R int = 0.060 3 standard reflections every 97 reflections intensity decay: none

Refinement

R[F 2 > 2σ(F 2)] = 0.054 wR(F 2) = 0.131 S = 1.00 3398 reflections 381 parameters 1 restraint H-atom parameters constrained Δρmax = 0.16 e Å−3 Δρmin = −0.22 e Å−3 Data collection: XSCANS (Bruker, 1997 ▶); cell refinement: XSCANS; data reduction: XSCANS; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL. Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536809026695/gk2215sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536809026695/gk2215Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C37H50N2O3F(000) = 1240
Mr = 570.79Dx = 1.172 Mg m3
Orthorhombic, P212121Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ac 2abCell parameters from 49 reflections
a = 8.7124 (19) Åθ = 2.1–15.1°
b = 19.054 (3) ŵ = 0.07 mm1
c = 19.480 (3) ÅT = 295 K
V = 3233.7 (10) Å3Prism, colorless
Z = 40.4 × 0.3 × 0.2 mm
Bruker P4 diffractometerRint = 0.060
Radiation source: fine-focus sealed tubeθmax = 25.5°, θmin = 2.1°
graphiteh = −1→10
ω scansk = −23→1
4315 measured reflectionsl = −1→23
3398 independent reflections3 standard reflections every 97 reflections
1649 reflections with I > 2σ(I) intensity decay: none
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.054H-atom parameters constrained
wR(F2) = 0.131w = 1/[σ2(Fo2) + (0.001P)2 + 1.8P] where P = (Fo2 + 2Fc2)/3
S = 1.00(Δ/σ)max = 0.008
3398 reflectionsΔρmax = 0.16 e Å3
381 parametersΔρmin = −0.22 e Å3
1 restraintExtinction correction: SHELXTL (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.00114 (8)
Experimental. absolute configuration has not been established by anomalous dispersion effects in diffraction measurements on the crystal. The enantiomer has been assigned by reference to unchanging chiral centres in the synthetic procedure. The Friedel pairs were averaged in the final refinement because the Mo Kα radiation was used and the compound was made of C, H, N and O.
Geometry. 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.
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
O11.1911 (2)0.29241 (10)0.64263 (10)0.0744 (7)
O20.4830 (2)0.57882 (10)0.26204 (9)0.0712 (6)
O30.2427 (2)0.55498 (10)0.29343 (10)0.0716 (6)
N11.0434 (3)0.26443 (11)0.64843 (12)0.0666 (8)
N21.1866 (3)0.35735 (12)0.60900 (12)0.0664 (8)
C10.9740 (3)0.42957 (13)0.55969 (15)0.0616 (9)
H1A1.04690.44750.52640.074*
H1B0.95140.46670.59220.074*
C21.0416 (3)0.36797 (13)0.59652 (13)0.0537 (8)
C30.9526 (3)0.31095 (13)0.62036 (14)0.0538 (8)
C40.7825 (3)0.30445 (13)0.61483 (14)0.0551 (9)
C50.7189 (3)0.37107 (12)0.57597 (13)0.0513 (8)
H5A0.70440.40640.61190.062*
C60.5586 (3)0.35847 (13)0.54702 (15)0.0601 (9)
H6A0.49630.33440.58090.072*
H6B0.56540.32890.50660.072*
C70.4830 (3)0.42843 (13)0.52804 (14)0.0584 (9)
H7A0.47050.45620.56940.070*
H7B0.38150.41910.50970.070*
C80.5739 (3)0.47144 (12)0.47542 (13)0.0486 (8)
C90.7459 (3)0.47566 (12)0.49632 (13)0.0478 (8)
H9A0.74810.50770.53570.057*
C100.8244 (3)0.40676 (12)0.52265 (14)0.0488 (8)
C110.8355 (3)0.51355 (12)0.44024 (14)0.0544 (8)
H11A0.93200.52990.45930.065*
H11B0.85930.48040.40400.065*
C120.7521 (3)0.57467 (13)0.40973 (13)0.0535 (8)
H12A0.80760.60330.38010.064*
C130.6062 (3)0.59207 (12)0.42089 (13)0.0476 (8)
C140.5073 (3)0.54920 (12)0.47100 (13)0.0482 (8)
C150.3371 (3)0.54676 (13)0.44892 (15)0.0582 (9)
H15A0.32450.50990.41500.070*
H15B0.27520.53440.48850.070*
C160.2764 (3)0.61563 (12)0.41882 (13)0.0555 (9)
H16A0.17170.60860.40340.067*
H16B0.27490.65100.45460.067*
C170.3727 (3)0.64233 (13)0.35880 (14)0.0527 (8)
C180.5388 (3)0.65564 (12)0.38321 (13)0.0528 (8)
H18A0.60140.66300.34200.063*
C190.5519 (3)0.72292 (12)0.42714 (13)0.0573 (9)
H19A0.50030.71510.47060.069*
H19B0.65940.73160.43690.069*
C200.4830 (4)0.78871 (12)0.39294 (14)0.0590 (9)
C210.3161 (3)0.77305 (13)0.37401 (14)0.0595 (9)
H21A0.25780.76480.41560.071*
H21B0.27240.81370.35120.071*
C220.3016 (3)0.70920 (13)0.32701 (14)0.0590 (9)
H22A0.35230.71920.28370.071*
H22B0.19390.70070.31750.071*
C230.7150 (4)0.30364 (15)0.68788 (14)0.0743 (10)
H23A0.75260.26330.71220.112*
H23B0.60500.30150.68530.112*
H23C0.74510.34550.71170.112*
C240.7422 (4)0.23391 (13)0.57912 (16)0.0779 (11)
H24A0.78360.23370.53340.117*
H24B0.63270.22870.57700.117*
H24C0.78530.19570.60480.117*
C250.8705 (3)0.35522 (13)0.46425 (14)0.0644 (9)
H25A0.78000.33940.44080.097*
H25B0.92330.31560.48350.097*
H25C0.93680.37880.43230.097*
C260.5545 (3)0.43558 (13)0.40356 (13)0.0616 (9)
H26A0.44780.42590.39560.092*
H26B0.61150.39250.40270.092*
H26C0.59220.46640.36840.092*
C270.5144 (3)0.58773 (12)0.54287 (12)0.0602 (9)
H27A0.47320.63420.53840.090*
H27B0.61910.59040.55800.090*
H27C0.45510.56190.57580.090*
C280.4855 (4)0.85000 (13)0.44522 (15)0.0815 (11)
H28A0.58970.86060.45730.122*
H28B0.42960.83670.48570.122*
H28C0.43860.89070.42510.122*
C290.5774 (4)0.81142 (14)0.33019 (15)0.0767 (11)
H29A0.57880.77410.29710.115*
H29B0.68050.82190.34420.115*
H29C0.53190.85250.31010.115*
C300.3771 (3)0.58947 (14)0.30003 (14)0.0593 (9)
C310.2337 (4)0.50425 (15)0.23783 (15)0.0753 (10)
H31A0.31750.47090.24100.090*
H31B0.23990.52780.19380.090*
C320.0835 (3)0.46753 (14)0.24481 (14)0.0614 (9)
C330.0760 (4)0.39893 (15)0.26336 (16)0.0816 (12)
H33A0.16680.37440.27080.098*
C34−0.0612 (4)0.36458 (17)0.27150 (17)0.0924 (13)
H34A−0.06340.31740.28370.111*
C35−0.1919 (4)0.40016 (18)0.26151 (17)0.0987 (13)
H35A−0.28490.37710.26820.118*
C36−0.1941 (4)0.4695 (2)0.24168 (16)0.0971 (13)
H36A−0.28580.49300.23340.116*
C37−0.0519 (4)0.50313 (16)0.23452 (15)0.0804 (11)
H37A−0.04900.55040.22260.096*
U11U22U33U12U13U23
O10.0625 (13)0.0800 (13)0.0808 (13)0.0098 (12)−0.0046 (12)0.0181 (12)
O20.0653 (12)0.0774 (12)0.0710 (12)−0.0048 (12)0.0123 (12)−0.0125 (11)
O30.0688 (13)0.0741 (11)0.0718 (12)−0.0144 (13)0.0066 (12)−0.0206 (11)
N10.0565 (15)0.0613 (13)0.0820 (16)0.0021 (14)−0.0040 (15)0.0038 (14)
N20.0561 (14)0.0712 (14)0.0720 (15)0.0048 (14)0.0006 (15)0.0129 (14)
C10.0469 (15)0.0509 (14)0.087 (2)−0.0029 (15)−0.0043 (17)0.0110 (16)
C20.0470 (16)0.0578 (15)0.0564 (16)0.0052 (15)0.0004 (15)−0.0019 (14)
C30.0513 (16)0.0497 (14)0.0603 (17)−0.0033 (15)−0.0011 (16)0.0004 (14)
C40.0536 (16)0.0426 (13)0.0691 (18)−0.0012 (14)−0.0076 (17)0.0090 (15)
C50.0541 (16)0.0429 (13)0.0570 (16)−0.0053 (14)−0.0005 (15)0.0004 (13)
C60.0482 (16)0.0533 (15)0.0789 (19)−0.0037 (15)−0.0041 (17)0.0129 (16)
C70.0508 (16)0.0536 (15)0.0708 (18)−0.0008 (15)−0.0001 (17)0.0126 (15)
C80.0447 (15)0.0458 (13)0.0553 (15)−0.0034 (14)0.0071 (14)−0.0011 (13)
C90.0456 (14)0.0447 (13)0.0531 (15)0.0027 (14)0.0036 (14)−0.0006 (13)
C100.0445 (15)0.0405 (13)0.0613 (16)−0.0005 (13)0.0034 (15)0.0068 (13)
C110.0519 (16)0.0456 (14)0.0656 (17)0.0032 (14)0.0037 (16)0.0070 (14)
C120.0586 (17)0.0491 (14)0.0530 (15)−0.0001 (16)0.0016 (16)0.0063 (14)
C130.0518 (16)0.0414 (13)0.0498 (15)0.0030 (14)0.0026 (15)0.0009 (13)
C140.0468 (15)0.0438 (13)0.0540 (15)0.0008 (13)0.0081 (15)0.0018 (13)
C150.0487 (16)0.0581 (16)0.0679 (17)0.0012 (15)0.0051 (16)0.0062 (16)
C160.0557 (17)0.0541 (15)0.0566 (16)0.0067 (16)−0.0029 (16)0.0062 (14)
C170.0530 (16)0.0514 (14)0.0537 (16)0.0034 (15)0.0049 (15)0.0054 (14)
C180.0619 (18)0.0429 (13)0.0536 (16)0.0046 (15)−0.0007 (16)0.0061 (13)
C190.0622 (18)0.0486 (14)0.0609 (17)0.0049 (16)−0.0081 (17)0.0037 (14)
C200.072 (2)0.0411 (13)0.0638 (17)−0.0008 (16)0.0027 (18)−0.0011 (14)
C210.0629 (18)0.0579 (16)0.0578 (17)0.0085 (17)−0.0036 (17)0.0028 (15)
C220.0648 (19)0.0524 (15)0.0598 (16)0.0023 (17)−0.0090 (17)0.0011 (15)
C230.066 (2)0.0791 (19)0.078 (2)−0.0034 (19)0.0058 (19)0.0283 (18)
C240.070 (2)0.0465 (15)0.117 (3)−0.0008 (18)−0.015 (2)−0.0007 (19)
C250.0627 (18)0.0582 (16)0.0722 (19)0.0106 (17)0.0095 (18)−0.0040 (16)
C260.0556 (17)0.0552 (15)0.0739 (19)−0.0023 (17)−0.0038 (18)−0.0032 (16)
C270.0718 (19)0.0519 (15)0.0568 (16)0.0080 (16)0.0083 (18)0.0032 (14)
C280.102 (3)0.0570 (17)0.085 (2)0.018 (2)−0.016 (2)−0.0103 (18)
C290.085 (2)0.0624 (17)0.083 (2)0.000 (2)0.006 (2)0.0221 (17)
C300.0629 (18)0.0577 (16)0.0572 (17)0.0024 (17)0.0026 (17)0.0015 (15)
C310.080 (2)0.0779 (18)0.0681 (18)−0.017 (2)0.005 (2)−0.0234 (17)
C320.0621 (18)0.0638 (17)0.0584 (17)0.0028 (17)0.0008 (17)−0.0110 (15)
C330.085 (2)0.0689 (19)0.091 (2)0.012 (2)−0.012 (2)−0.0114 (19)
C340.109 (3)0.0729 (19)0.095 (2)−0.023 (2)0.015 (3)−0.013 (2)
C350.089 (2)0.125 (3)0.082 (2)−0.034 (2)0.013 (2)−0.043 (2)
C360.073 (2)0.146 (3)0.071 (2)0.032 (3)−0.014 (2)−0.023 (2)
C370.090 (2)0.078 (2)0.074 (2)0.011 (2)−0.005 (2)−0.0125 (18)
O1—N11.398 (3)C17—C221.546 (4)
O1—N21.401 (3)C18—C191.545 (3)
O2—C301.200 (3)C18—H18A0.9800
O3—C301.349 (3)C19—C201.541 (3)
O3—C311.454 (3)C19—H19A0.9700
N1—C31.308 (3)C19—H19B0.9700
N2—C21.302 (4)C20—C211.529 (4)
C1—C21.497 (4)C20—C291.536 (4)
C1—C101.551 (4)C20—C281.550 (4)
C1—H1A0.9700C21—C221.528 (4)
C1—H1B0.9700C21—H21A0.9700
C2—C31.413 (4)C21—H21B0.9700
C3—C41.491 (4)C22—H22A0.9700
C4—C231.540 (4)C22—H22B0.9700
C4—C241.554 (4)C23—H23A0.9600
C4—C51.579 (3)C23—H23B0.9600
C5—C61.525 (4)C23—H23C0.9600
C5—C101.545 (4)C24—H24A0.9600
C5—H5A0.9800C24—H24B0.9600
C6—C71.532 (3)C24—H24C0.9600
C6—H6A0.9700C25—H25A0.9600
C6—H6B0.9700C25—H25B0.9600
C7—C81.533 (3)C25—H25C0.9600
C7—H7A0.9700C26—H26A0.9600
C7—H7B0.9700C26—H26B0.9600
C8—C91.555 (4)C26—H26C0.9600
C8—C261.567 (3)C27—H27A0.9600
C8—C141.593 (3)C27—H27B0.9600
C9—C111.524 (3)C27—H27C0.9600
C9—C101.567 (3)C28—H28A0.9600
C9—H9A0.9800C28—H28B0.9600
C10—C251.556 (4)C28—H28C0.9600
C11—C121.496 (3)C29—H29A0.9600
C11—H11A0.9700C29—H29B0.9600
C11—H11B0.9700C29—H29C0.9600
C12—C131.332 (4)C31—C321.490 (4)
C12—H12A0.9300C31—H31A0.9700
C13—C181.533 (3)C31—H31B0.9700
C13—C141.537 (3)C32—C331.358 (4)
C14—C151.545 (4)C32—C371.376 (4)
C14—C271.582 (3)C33—C341.372 (5)
C15—C161.531 (3)C33—H33A0.9300
C15—H15A0.9700C34—C351.340 (5)
C15—H15B0.9700C34—H34A0.9300
C16—C171.526 (4)C35—C361.377 (5)
C16—H16A0.9700C35—H35A0.9300
C16—H16B0.9700C36—C371.402 (5)
C17—C301.525 (4)C36—H36A0.9300
C17—C181.544 (4)C37—H37A0.9300
N1—O1—N2110.42 (19)C13—C18—H18A107.0
C30—O3—C31116.2 (2)C17—C18—H18A107.0
C3—N1—O1105.3 (2)C19—C18—H18A107.0
C2—N2—O1104.6 (2)C20—C19—C18114.0 (2)
C2—C1—C10109.5 (2)C20—C19—H19A108.8
C2—C1—H1A109.8C18—C19—H19A108.8
C10—C1—H1A109.8C20—C19—H19B108.8
C2—C1—H1B109.8C18—C19—H19B108.8
C10—C1—H1B109.8H19A—C19—H19B107.6
H1A—C1—H1B108.2C21—C20—C29111.9 (2)
N2—C2—C3110.6 (2)C21—C20—C19108.4 (2)
N2—C2—C1126.4 (2)C29—C20—C19111.4 (2)
C3—C2—C1123.0 (2)C21—C20—C28108.6 (2)
N1—C3—C2109.1 (2)C29—C20—C28107.7 (2)
N1—C3—C4125.1 (2)C19—C20—C28108.9 (2)
C2—C3—C4125.8 (2)C22—C21—C20112.2 (2)
C3—C4—C23108.3 (2)C22—C21—H21A109.2
C3—C4—C24109.2 (2)C20—C21—H21A109.2
C23—C4—C24108.6 (2)C22—C21—H21B109.2
C3—C4—C5108.5 (2)C20—C21—H21B109.2
C23—C4—C5108.5 (2)H21A—C21—H21B107.9
C24—C4—C5113.7 (2)C21—C22—C17112.5 (2)
C6—C5—C10111.5 (2)C21—C22—H22A109.1
C6—C5—C4111.9 (2)C17—C22—H22A109.1
C10—C5—C4117.8 (2)C21—C22—H22B109.1
C6—C5—H5A104.8C17—C22—H22B109.1
C10—C5—H5A104.8H22A—C22—H22B107.8
C4—C5—H5A104.8C4—C23—H23A109.5
C5—C6—C7110.2 (2)C4—C23—H23B109.5
C5—C6—H6A109.6H23A—C23—H23B109.5
C7—C6—H6A109.6C4—C23—H23C109.5
C5—C6—H6B109.6H23A—C23—H23C109.5
C7—C6—H6B109.6H23B—C23—H23C109.5
H6A—C6—H6B108.1C4—C24—H24A109.5
C6—C7—C8113.8 (2)C4—C24—H24B109.5
C6—C7—H7A108.8H24A—C24—H24B109.5
C8—C7—H7A108.8C4—C24—H24C109.5
C6—C7—H7B108.8H24A—C24—H24C109.5
C8—C7—H7B108.8H24B—C24—H24C109.5
H7A—C7—H7B107.7C10—C25—H25A109.5
C7—C8—C9110.5 (2)C10—C25—H25B109.5
C7—C8—C26107.9 (2)H25A—C25—H25B109.5
C9—C8—C26111.2 (2)C10—C25—H25C109.5
C7—C8—C14110.2 (2)H25A—C25—H25C109.5
C9—C8—C14108.48 (19)H25B—C25—H25C109.5
C26—C8—C14108.5 (2)C8—C26—H26A109.5
C11—C9—C8109.3 (2)C8—C26—H26B109.5
C11—C9—C10114.1 (2)H26A—C26—H26B109.5
C8—C9—C10117.6 (2)C8—C26—H26C109.5
C11—C9—H9A104.8H26A—C26—H26C109.5
C8—C9—H9A104.8H26B—C26—H26C109.5
C10—C9—H9A104.8C14—C27—H27A109.5
C5—C10—C1108.1 (2)C14—C27—H27B109.5
C5—C10—C25111.6 (2)H27A—C27—H27B109.5
C1—C10—C25107.5 (2)C14—C27—H27C109.5
C5—C10—C9109.2 (2)H27A—C27—H27C109.5
C1—C10—C9106.51 (19)H27B—C27—H27C109.5
C25—C10—C9113.7 (2)C20—C28—H28A109.5
C12—C11—C9113.9 (2)C20—C28—H28B109.5
C12—C11—H11A108.8H28A—C28—H28B109.5
C9—C11—H11A108.8C20—C28—H28C109.5
C12—C11—H11B108.8H28A—C28—H28C109.5
C9—C11—H11B108.8H28B—C28—H28C109.5
H11A—C11—H11B107.7C20—C29—H29A109.5
C13—C12—C11126.4 (2)C20—C29—H29B109.5
C13—C12—H12A116.8H29A—C29—H29B109.5
C11—C12—H12A116.8C20—C29—H29C109.5
C12—C13—C18119.0 (2)H29A—C29—H29C109.5
C12—C13—C14120.4 (2)H29B—C29—H29C109.5
C18—C13—C14120.6 (2)O2—C30—O3121.8 (3)
C13—C14—C15112.1 (2)O2—C30—C17126.4 (3)
C13—C14—C27107.1 (2)O3—C30—C17111.8 (2)
C15—C14—C27107.3 (2)O3—C31—C32106.9 (2)
C13—C14—C8108.9 (2)O3—C31—H31A110.3
C15—C14—C8109.7 (2)C32—C31—H31A110.3
C27—C14—C8111.70 (19)O3—C31—H31B110.3
C16—C15—C14114.4 (2)C32—C31—H31B110.3
C16—C15—H15A108.7H31A—C31—H31B108.6
C14—C15—H15A108.7C33—C32—C37118.2 (3)
C16—C15—H15B108.7C33—C32—C31121.2 (3)
C14—C15—H15B108.7C37—C32—C31120.6 (3)
H15A—C15—H15B107.6C32—C33—C34122.1 (3)
C17—C16—C15112.9 (2)C32—C33—H33A118.9
C17—C16—H16A109.0C34—C33—H33A118.9
C15—C16—H16A109.0C35—C34—C33118.9 (3)
C17—C16—H16B109.0C35—C34—H34A120.6
C15—C16—H16B109.0C33—C34—H34A120.6
H16A—C16—H16B107.8C34—C35—C36122.5 (4)
C30—C17—C16111.6 (2)C34—C35—H35A118.7
C30—C17—C18108.4 (2)C36—C35—H35A118.7
C16—C17—C18109.5 (2)C35—C36—C37117.1 (3)
C30—C17—C22104.7 (2)C35—C36—H36A121.5
C16—C17—C22111.2 (2)C37—C36—H36A121.5
C18—C17—C22111.3 (2)C32—C37—C36121.2 (3)
C13—C18—C17112.1 (2)C32—C37—H37A119.4
C13—C18—C19111.2 (2)C36—C37—H37A119.4
C17—C18—C19112.1 (2)
N2—O1—N1—C3−0.9 (3)C12—C13—C14—C8−25.8 (3)
N1—O1—N2—C21.1 (3)C18—C13—C14—C8154.5 (2)
O1—N2—C2—C3−0.9 (3)C7—C8—C14—C13176.9 (2)
O1—N2—C2—C1−178.5 (2)C9—C8—C14—C1355.8 (3)
C10—C1—C2—N2150.4 (3)C26—C8—C14—C13−65.1 (3)
C10—C1—C2—C3−26.9 (4)C7—C8—C14—C15−60.0 (3)
O1—N1—C3—C20.3 (3)C9—C8—C14—C15178.9 (2)
O1—N1—C3—C4−179.5 (2)C26—C8—C14—C1558.0 (3)
N2—C2—C3—N10.4 (3)C7—C8—C14—C2758.9 (3)
C1—C2—C3—N1178.1 (2)C9—C8—C14—C27−62.3 (3)
N2—C2—C3—C4−179.8 (3)C26—C8—C14—C27176.8 (2)
C1—C2—C3—C4−2.1 (4)C13—C14—C15—C16−38.5 (3)
N1—C3—C4—C2363.8 (3)C27—C14—C15—C1678.8 (3)
C2—C3—C4—C23−116.0 (3)C8—C14—C15—C16−159.6 (2)
N1—C3—C4—C24−54.2 (4)C14—C15—C16—C1754.7 (3)
C2—C3—C4—C24125.9 (3)C15—C16—C17—C3059.8 (3)
N1—C3—C4—C5−178.6 (2)C15—C16—C17—C18−60.3 (3)
C2—C3—C4—C51.6 (4)C15—C16—C17—C22176.3 (2)
C3—C4—C5—C6160.9 (2)C12—C13—C18—C17140.0 (2)
C23—C4—C5—C6−81.6 (3)C14—C13—C18—C17−40.2 (3)
C24—C4—C5—C639.2 (3)C12—C13—C18—C19−93.6 (3)
C3—C4—C5—C1029.8 (3)C14—C13—C18—C1986.1 (3)
C23—C4—C5—C10147.2 (2)C30—C17—C18—C13−70.7 (3)
C24—C4—C5—C10−91.9 (3)C16—C17—C18—C1351.4 (3)
C10—C5—C6—C7−61.6 (3)C22—C17—C18—C13174.7 (2)
C4—C5—C6—C7164.1 (2)C30—C17—C18—C19163.4 (2)
C5—C6—C7—C858.4 (3)C16—C17—C18—C19−74.6 (3)
C6—C7—C8—C9−47.9 (3)C22—C17—C18—C1948.8 (3)
C6—C7—C8—C2673.9 (3)C13—C18—C19—C20−178.7 (2)
C6—C7—C8—C14−167.8 (2)C17—C18—C19—C20−52.3 (3)
C7—C8—C9—C11175.45 (19)C18—C19—C20—C2155.3 (3)
C26—C8—C9—C1155.6 (3)C18—C19—C20—C29−68.2 (3)
C14—C8—C9—C11−63.7 (2)C18—C19—C20—C28173.2 (2)
C7—C8—C9—C1043.3 (3)C29—C20—C21—C2266.0 (3)
C26—C8—C9—C10−76.5 (3)C19—C20—C21—C22−57.2 (3)
C14—C8—C9—C10164.2 (2)C28—C20—C21—C22−175.3 (2)
C6—C5—C10—C1170.1 (2)C20—C21—C22—C1757.3 (3)
C4—C5—C10—C1−58.6 (3)C30—C17—C22—C21−168.8 (2)
C6—C5—C10—C25−72.0 (3)C16—C17—C22—C2170.6 (3)
C4—C5—C10—C2559.3 (3)C18—C17—C22—C21−51.8 (3)
C6—C5—C10—C954.6 (3)C31—O3—C30—O20.1 (4)
C4—C5—C10—C9−174.1 (2)C31—O3—C30—C17178.8 (2)
C2—C1—C10—C553.2 (3)C16—C17—C30—O2−145.9 (3)
C2—C1—C10—C25−67.3 (3)C18—C17—C30—O2−25.2 (4)
C2—C1—C10—C9170.4 (2)C22—C17—C30—O293.7 (3)
C11—C9—C10—C5−176.7 (2)C16—C17—C30—O335.4 (3)
C8—C9—C10—C5−46.8 (3)C18—C17—C30—O3156.1 (2)
C11—C9—C10—C166.8 (3)C22—C17—C30—O3−85.0 (3)
C8—C9—C10—C1−163.3 (2)C30—O3—C31—C32174.1 (2)
C11—C9—C10—C25−51.4 (3)O3—C31—C32—C33−111.0 (3)
C8—C9—C10—C2578.5 (3)O3—C31—C32—C3767.0 (3)
C8—C9—C11—C1239.5 (3)C37—C32—C33—C340.5 (5)
C10—C9—C11—C12173.5 (2)C31—C32—C33—C34178.6 (3)
C9—C11—C12—C13−8.8 (4)C32—C33—C34—C35−0.7 (5)
C11—C12—C13—C18−178.2 (2)C33—C34—C35—C361.7 (5)
C11—C12—C13—C142.1 (4)C34—C35—C36—C37−2.3 (5)
C12—C13—C14—C15−147.4 (2)C33—C32—C37—C36−1.1 (4)
C18—C13—C14—C1532.9 (3)C31—C32—C37—C36−179.3 (3)
C12—C13—C14—C2795.2 (3)C35—C36—C37—C322.0 (5)
C18—C13—C14—C27−84.6 (3)
  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

Review 2.  Oleanolic acid and ursolic acid: research perspectives.

Authors:  Jie Liu
Journal:  J Ethnopharmacol       Date:  2005-08-22       Impact factor: 4.360

3.  Pentacyclic triterpenes. Part 3: Synthesis and biological evaluation of oleanolic acid derivatives as novel inhibitors of glycogen phosphorylase.

Authors:  Jun Chen; Jun Liu; Luyong Zhang; Guanzhong Wu; Weiyi Hua; Xiaoming Wu; Hongbin Sun
Journal:  Bioorg Med Chem Lett       Date:  2006-03-20       Impact factor: 2.823

  3 in total

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