Literature DB >> 21754518

Absolute configuration of 3β-acet-oxy-olean-11,12-aziridin-28,13-β-olide.

Wen Nee Tan, Keng Chong Wong, Melati Khairuddean, Madhukar Hemamalini, Hoong-Kun Fun.   

Abstract

The title compound, C(32)H(49)NO(4), has been isolated from the dichloro-methane extract of the stem bark of Garcinia atroviridis Griff. ex T. Anders. Rings A and B, B and C, and C and D are trans-fused, whereas rings D and E are cis-fused. Rings A, B, C and E have slightly distorted chair conformations, while ring D is most heavily distorted towards a half-chair conformation owing to the strain induced by the lactonization. The ester group attached to ring A is in an equatorial position.

Entities:  

Year:  2011        PMID: 21754518      PMCID: PMC3089217          DOI: 10.1107/S1600536811014875

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


Related literature

For details and applications of Garcinia atroviridis Griff. ex T. Anders, see: Permana et al. (2001 ▶); Amran et al. (2009 ▶). For bond-length data, see: Allen et al. (1987 ▶). For ring conformations, see: Cremer & Pople (1975 ▶). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986 ▶).

Experimental

Crystal data

C32H49NO4 M = 511.72 Monoclinic, a = 13.0197 (2) Å b = 6.7460 (1) Å c = 32.0674 (5) Å β = 100.6452 (4)° V = 2768.04 (7) Å3 Z = 4 Cu Kα radiation μ = 0.62 mm−1 T = 100 K 0.73 × 0.15 × 0.14 mm

Data collection

Bruker SMART APEX DUO CCD area-detector diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2009 ▶) T min = 0.659, T max = 0.917 8407 measured reflections 3061 independent reflections 3050 reflections with I > 2σ(I) R int = 0.018

Refinement

R[F 2 > 2σ(F 2)] = 0.033 wR(F 2) = 0.087 S = 1.02 3061 reflections 342 parameters 1 restraint H-atom parameters constrained Δρmax = 0.32 e Å−3 Δρmin = −0.37 e Å−3 Absolute structure: Flack (1983 ▶), 721 Friedel pairs Flack parameter: 0.1 (2) Data collection: APEX2 (Bruker, 2009 ▶); cell refinement: SAINT (Bruker, 2009 ▶); data reduction: SAINT; 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 and PLATON (Spek, 2009 ▶). Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536811014875/is2699sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536811014875/is2699Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C32H49NO4F(000) = 1120
Mr = 511.72Dx = 1.228 Mg m3
Monoclinic, C2Cu Kα radiation, λ = 1.54178 Å
Hall symbol: C 2yCell parameters from 8407 reflections
a = 13.0197 (2) Åθ = 4.2–62.5°
b = 6.7460 (1) ŵ = 0.62 mm1
c = 32.0674 (5) ÅT = 100 K
β = 100.6452 (4)°Block, colourless
V = 2768.04 (7) Å30.73 × 0.15 × 0.14 mm
Z = 4
Bruker SMART APEX DUO CCD area-detector diffractometer3061 independent reflections
Radiation source: fine-focus sealed tube3050 reflections with I > 2σ(I)
graphiteRint = 0.018
φ and ω scansθmax = 62.5°, θmin = 4.2°
Absorption correction: multi-scan (SADABS; Bruker, 2009)h = −14→14
Tmin = 0.659, Tmax = 0.917k = −7→5
8407 measured reflectionsl = −36→36
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.033H-atom parameters constrained
wR(F2) = 0.087w = 1/[σ2(Fo2) + (0.0534P)2 + 1.724P] where P = (Fo2 + 2Fc2)/3
S = 1.02(Δ/σ)max = 0.001
3061 reflectionsΔρmax = 0.32 e Å3
342 parametersΔρmin = −0.37 e Å3
1 restraintAbsolute structure: Flack (1983), 721 Friedel pairs
Primary atom site location: structure-invariant direct methodsFlack parameter: 0.1 (2)
Experimental. The crystal was placed in the cold stream of an Oxford Cryosystems Cobra open-flow nitrogen cryostat (Cosier & Glazer, 1986) operating at 100.0 (1) K.
Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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 > 2σ(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
O10.32106 (11)−0.0737 (2)0.17064 (4)0.0246 (3)
O20.62607 (11)0.4500 (2)0.44068 (4)0.0270 (4)
O30.67821 (13)0.7573 (3)0.42805 (4)0.0378 (4)
O40.19103 (13)−0.2023 (3)0.12291 (5)0.0355 (4)
N10.55624 (13)0.2185 (4)0.21012 (6)0.0339 (5)
H10.59370.31720.20300.041*
C10.24506 (16)−0.0616 (4)0.13528 (6)0.0246 (5)
C20.24394 (14)0.1455 (3)0.11795 (6)0.0205 (4)
C30.21283 (15)0.1641 (4)0.06963 (6)0.0218 (4)
H3A0.13630.14780.06110.026*
H3B0.24720.05820.05580.026*
C40.24546 (15)0.3678 (4)0.05499 (6)0.0243 (5)
H4A0.20390.47150.06610.029*
H4B0.22830.37340.02360.029*
C50.36277 (16)0.4152 (4)0.06945 (6)0.0256 (5)
C60.39041 (15)0.4014 (4)0.11863 (6)0.0234 (5)
H6A0.46630.42290.12830.028*
H6B0.35250.50550.13140.028*
C70.36000 (15)0.1978 (3)0.13284 (6)0.0196 (4)
H7A0.39930.10120.11810.023*
C80.37372 (15)0.1226 (3)0.17907 (6)0.0197 (4)
C90.31546 (14)0.2417 (3)0.20917 (5)0.0169 (4)
C100.19759 (14)0.2301 (4)0.19046 (5)0.0217 (4)
H10A0.15990.32870.20490.026*
H10B0.17130.09690.19610.026*
C110.17391 (14)0.2695 (4)0.14213 (5)0.0214 (4)
H11A0.18450.41200.13690.026*
H11B0.09970.23770.13090.026*
C120.48492 (15)0.0697 (4)0.19851 (6)0.0282 (5)
H12A0.5131−0.04800.18540.034*
C130.52441 (15)0.0924 (4)0.24330 (6)0.0304 (6)
H13A0.5763−0.00870.25680.036*
C140.46077 (14)0.1942 (3)0.27216 (5)0.0184 (4)
H14A0.46920.33910.26720.022*
C150.50418 (14)0.1640 (3)0.32060 (6)0.0194 (4)
C160.61602 (14)0.2523 (4)0.32994 (6)0.0234 (5)
H16A0.66390.16250.31830.028*
H16B0.61580.38140.31530.028*
C170.65743 (15)0.2823 (4)0.37752 (6)0.0243 (5)
H17A0.66270.15280.39230.029*
H17B0.72800.34230.38180.029*
C180.58362 (15)0.4169 (3)0.39561 (5)0.0230 (5)
H18A0.58010.54720.38050.028*
C190.47224 (15)0.3357 (3)0.39178 (6)0.0222 (5)
C200.43358 (14)0.2950 (3)0.34356 (5)0.0192 (4)
H20A0.43390.42810.32990.023*
C210.31921 (14)0.2264 (4)0.33240 (5)0.0218 (4)
H21A0.31460.08430.33960.026*
H21B0.27650.30260.34930.026*
C220.27630 (14)0.2569 (4)0.28508 (5)0.0217 (4)
H22A0.27410.40070.27880.026*
H22B0.20380.20610.27850.026*
C230.34200 (14)0.1521 (3)0.25602 (6)0.0183 (4)
C240.66861 (15)0.6269 (3)0.45241 (6)0.0240 (5)
C250.7020 (2)0.6407 (4)0.49973 (7)0.0368 (6)
H25A0.66680.75330.51040.055*
H25B0.77780.65980.50680.055*
H25C0.68310.51820.51290.055*
C260.43081 (16)0.2772 (4)0.04793 (6)0.0336 (6)
H26A0.50470.30780.05820.050*
H26B0.41400.29640.01710.050*
H26C0.41710.13910.05470.050*
C270.38219 (18)0.6281 (4)0.05690 (6)0.0342 (6)
H27A0.45480.66470.06840.051*
H27B0.33490.71740.06840.051*
H27C0.36930.63910.02590.051*
C280.34752 (16)0.4625 (3)0.20954 (6)0.0227 (5)
H28A0.30000.53370.18730.034*
H28B0.41920.47310.20430.034*
H28C0.34380.52050.23720.034*
C290.51138 (16)−0.0556 (4)0.33404 (6)0.0255 (5)
H29A0.5653−0.07110.35950.038*
H29B0.5296−0.13620.31100.038*
H29C0.4438−0.09920.34010.038*
C300.40528 (17)0.5014 (4)0.40603 (6)0.0296 (5)
H30A0.43920.55060.43390.044*
H30B0.33600.44900.40780.044*
H30C0.39800.61010.38540.044*
C310.46755 (16)0.1551 (4)0.42054 (6)0.0270 (5)
H31A0.48450.19640.45030.040*
H31B0.51810.05540.41500.040*
H31C0.39710.09840.41460.040*
C320.31756 (17)−0.0706 (3)0.25724 (6)0.0246 (5)
H32A0.3163−0.11050.28650.037*
H32B0.3716−0.14600.24650.037*
H32C0.2493−0.09710.23950.037*
U11U22U33U12U13U23
O10.0363 (8)0.0157 (8)0.0206 (6)0.0029 (7)0.0019 (5)−0.0023 (6)
O20.0373 (8)0.0246 (9)0.0164 (6)−0.0043 (7)−0.0025 (5)0.0014 (6)
O30.0515 (9)0.0313 (10)0.0270 (7)−0.0149 (9)−0.0024 (6)0.0025 (8)
O40.0508 (9)0.0236 (10)0.0292 (7)−0.0085 (8)0.0001 (7)−0.0039 (7)
N10.0171 (8)0.0479 (14)0.0367 (9)−0.0027 (9)0.0048 (7)−0.0081 (10)
C10.0309 (10)0.0235 (13)0.0194 (9)−0.0020 (10)0.0045 (7)−0.0024 (9)
C20.0205 (9)0.0193 (11)0.0212 (9)0.0002 (9)0.0024 (7)−0.0009 (9)
C30.0224 (9)0.0237 (12)0.0180 (9)−0.0003 (9)0.0001 (7)−0.0030 (8)
C40.0265 (10)0.0295 (13)0.0157 (8)−0.0002 (10)0.0008 (7)0.0017 (9)
C50.0271 (10)0.0305 (14)0.0188 (9)−0.0020 (10)0.0033 (7)0.0029 (9)
C60.0196 (9)0.0314 (14)0.0185 (9)−0.0025 (9)0.0017 (7)0.0008 (9)
C70.0203 (9)0.0213 (13)0.0173 (8)0.0031 (8)0.0038 (7)−0.0021 (8)
C80.0231 (9)0.0150 (12)0.0210 (9)0.0025 (9)0.0043 (7)−0.0018 (8)
C90.0182 (9)0.0143 (11)0.0183 (8)0.0028 (8)0.0035 (7)−0.0014 (8)
C100.0199 (9)0.0254 (12)0.0200 (9)0.0040 (9)0.0043 (7)−0.0003 (9)
C110.0185 (8)0.0236 (12)0.0205 (9)0.0019 (9)−0.0003 (7)−0.0001 (9)
C120.0246 (10)0.0370 (15)0.0241 (10)0.0137 (11)0.0074 (8)−0.0003 (10)
C130.0234 (9)0.0482 (17)0.0193 (9)0.0122 (11)0.0035 (8)−0.0008 (10)
C140.0198 (9)0.0177 (12)0.0177 (8)0.0022 (8)0.0036 (7)−0.0008 (8)
C150.0205 (9)0.0210 (12)0.0163 (8)0.0031 (9)0.0025 (7)−0.0002 (8)
C160.0205 (9)0.0301 (13)0.0195 (9)0.0031 (9)0.0034 (7)0.0017 (9)
C170.0225 (9)0.0295 (13)0.0195 (9)−0.0016 (10)0.0006 (7)0.0038 (9)
C180.0318 (10)0.0221 (13)0.0135 (8)−0.0025 (10)−0.0005 (7)0.0010 (9)
C190.0280 (10)0.0217 (12)0.0176 (9)0.0017 (9)0.0059 (7)−0.0002 (8)
C200.0224 (9)0.0182 (12)0.0172 (8)0.0023 (9)0.0041 (7)0.0020 (8)
C210.0217 (9)0.0256 (12)0.0194 (9)0.0003 (9)0.0072 (7)−0.0019 (9)
C220.0193 (8)0.0243 (12)0.0216 (9)0.0035 (9)0.0042 (7)−0.0007 (9)
C230.0194 (9)0.0168 (11)0.0191 (9)0.0013 (8)0.0044 (7)−0.0022 (8)
C240.0228 (9)0.0257 (13)0.0228 (10)0.0004 (10)0.0019 (7)0.0003 (10)
C250.0522 (13)0.0316 (15)0.0242 (10)−0.0048 (12)0.0009 (9)−0.0020 (10)
C260.0277 (10)0.0529 (18)0.0213 (9)0.0005 (12)0.0069 (8)−0.0001 (11)
C270.0378 (11)0.0404 (16)0.0229 (10)−0.0111 (12)0.0018 (9)0.0070 (10)
C280.0300 (10)0.0180 (12)0.0192 (9)0.0017 (9)0.0021 (7)−0.0006 (9)
C290.0321 (10)0.0210 (12)0.0213 (9)0.0071 (10)−0.0005 (8)−0.0009 (9)
C300.0349 (11)0.0317 (15)0.0215 (9)0.0058 (10)0.0038 (8)−0.0042 (9)
C310.0317 (10)0.0299 (13)0.0195 (9)−0.0041 (10)0.0053 (8)0.0015 (9)
C320.0342 (11)0.0181 (12)0.0210 (9)−0.0048 (10)0.0033 (8)0.0016 (9)
O1—C11.363 (2)C15—C201.555 (3)
O1—C81.493 (3)C16—C171.535 (2)
O2—C241.340 (3)C16—H16A0.9900
O2—C181.466 (2)C16—H16B0.9900
O3—C241.198 (3)C17—C181.514 (3)
O4—C11.204 (3)C17—H17A0.9900
N1—C121.371 (3)C17—H17B0.9900
N1—C131.480 (3)C18—C191.534 (3)
N1—H10.8800C18—H18A1.0000
C1—C21.502 (3)C19—C311.536 (3)
C2—C31.533 (2)C19—C301.538 (3)
C2—C71.539 (3)C19—C201.560 (2)
C2—C111.547 (3)C20—C211.537 (2)
C3—C41.537 (3)C20—H20A1.0000
C3—H3A0.9900C21—C221.531 (2)
C3—H3B0.9900C21—H21A0.9900
C4—C51.546 (3)C21—H21B0.9900
C4—H4A0.9900C22—C231.547 (3)
C4—H4B0.9900C22—H22A0.9900
C5—C271.525 (4)C22—H22B0.9900
C5—C261.534 (3)C23—C321.538 (3)
C5—C61.554 (2)C24—C251.502 (3)
C6—C71.522 (3)C25—H25A0.9800
C6—H6A0.9900C25—H25B0.9800
C6—H6B0.9900C25—H25C0.9800
C7—C81.546 (2)C26—H26A0.9800
C7—H7A1.0000C26—H26B0.9800
C8—C121.510 (3)C26—H26C0.9800
C8—C91.557 (2)C27—H27A0.9800
C9—C101.543 (2)C27—H27B0.9800
C9—C281.546 (3)C27—H27C0.9800
C9—C231.597 (2)C28—H28A0.9800
C10—C111.546 (2)C28—H28B0.9800
C10—H10A0.9900C28—H28C0.9800
C10—H10B0.9900C29—H29A0.9800
C11—H11A0.9900C29—H29B0.9800
C11—H11B0.9900C29—H29C0.9800
C12—C131.442 (3)C30—H30A0.9800
C12—H12A1.0000C30—H30B0.9800
C13—C141.516 (3)C30—H30C0.9800
C13—H13A1.0000C31—H31A0.9800
C14—C231.563 (2)C31—H31B0.9800
C14—C151.565 (2)C31—H31C0.9800
C14—H14A1.0000C32—H32A0.9800
C15—C291.541 (3)C32—H32B0.9800
C15—C161.550 (3)C32—H32C0.9800
C1—O1—C8109.63 (16)C15—C16—H16B109.0
C24—O2—C18118.26 (16)H16A—C16—H16B107.8
C12—N1—C1360.61 (15)C18—C17—C16109.20 (15)
C12—N1—H1149.7C18—C17—H17A109.8
C13—N1—H1149.7C16—C17—H17A109.8
O4—C1—O1121.1 (2)C18—C17—H17B109.8
O4—C1—C2130.24 (18)C16—C17—H17B109.8
O1—C1—C2108.64 (18)H17A—C17—H17B108.3
C1—C2—C3115.65 (17)O2—C18—C17108.59 (15)
C1—C2—C799.01 (16)O2—C18—C19108.18 (14)
C3—C2—C7110.84 (15)C17—C18—C19114.38 (18)
C1—C2—C11106.48 (16)O2—C18—H18A108.5
C3—C2—C11113.10 (16)C17—C18—H18A108.5
C7—C2—C11110.87 (16)C19—C18—H18A108.5
C2—C3—C4110.22 (16)C18—C19—C31112.16 (16)
C2—C3—H3A109.6C18—C19—C30107.22 (18)
C4—C3—H3A109.6C31—C19—C30108.08 (16)
C2—C3—H3B109.6C18—C19—C20105.63 (14)
C4—C3—H3B109.6C31—C19—C20114.48 (18)
H3A—C3—H3B108.1C30—C19—C20109.00 (16)
C3—C4—C5114.01 (17)C21—C20—C15110.54 (16)
C3—C4—H4A108.8C21—C20—C19113.90 (14)
C5—C4—H4A108.8C15—C20—C19117.30 (15)
C3—C4—H4B108.8C21—C20—H20A104.5
C5—C4—H4B108.8C15—C20—H20A104.5
H4A—C4—H4B107.6C19—C20—H20A104.5
C27—C5—C26108.38 (18)C22—C21—C20110.53 (15)
C27—C5—C4108.57 (18)C22—C21—H21A109.5
C26—C5—C4111.10 (18)C20—C21—H21A109.5
C27—C5—C6107.80 (18)C22—C21—H21B109.5
C26—C5—C6112.04 (17)C20—C21—H21B109.5
C4—C5—C6108.83 (15)H21A—C21—H21B108.1
C7—C6—C5109.49 (17)C21—C22—C23113.23 (16)
C7—C6—H6A109.8C21—C22—H22A108.9
C5—C6—H6A109.8C23—C22—H22A108.9
C7—C6—H6B109.8C21—C22—H22B108.9
C5—C6—H6B109.8C23—C22—H22B108.9
H6A—C6—H6B108.2H22A—C22—H22B107.7
C6—C7—C2114.13 (17)C32—C23—C22106.92 (17)
C6—C7—C8126.37 (17)C32—C23—C14111.44 (17)
C2—C7—C898.92 (15)C22—C23—C14109.92 (15)
C6—C7—H7A105.2C32—C23—C9112.57 (16)
C2—C7—H7A105.2C22—C23—C9110.26 (16)
C8—C7—H7A105.2C14—C23—C9105.77 (14)
O1—C8—C12103.81 (17)O3—C24—O2123.95 (18)
O1—C8—C798.61 (14)O3—C24—C25124.6 (2)
C12—C8—C7113.93 (15)O2—C24—C25111.48 (19)
O1—C8—C9108.06 (14)C24—C25—H25A109.5
C12—C8—C9113.95 (15)C24—C25—H25B109.5
C7—C8—C9116.24 (17)H25A—C25—H25B109.5
C10—C9—C28107.43 (17)C24—C25—H25C109.5
C10—C9—C8107.23 (15)H25A—C25—H25C109.5
C28—C9—C8109.88 (15)H25B—C25—H25C109.5
C10—C9—C23111.93 (15)C5—C26—H26A109.5
C28—C9—C23110.24 (16)C5—C26—H26B109.5
C8—C9—C23110.04 (16)H26A—C26—H26B109.5
C9—C10—C11112.39 (14)C5—C26—H26C109.5
C9—C10—H10A109.1H26A—C26—H26C109.5
C11—C10—H10A109.1H26B—C26—H26C109.5
C9—C10—H10B109.1C5—C27—H27A109.5
C11—C10—H10B109.1C5—C27—H27B109.5
H10A—C10—H10B107.9H27A—C27—H27B109.5
C10—C11—C2112.49 (16)C5—C27—H27C109.5
C10—C11—H11A109.1H27A—C27—H27C109.5
C2—C11—H11A109.1H27B—C27—H27C109.5
C10—C11—H11B109.1C9—C28—H28A109.5
C2—C11—H11B109.1C9—C28—H28B109.5
H11A—C11—H11B107.8H28A—C28—H28B109.5
N1—C12—C1363.43 (16)C9—C28—H28C109.5
N1—C12—C8119.3 (2)H28A—C28—H28C109.5
C13—C12—C8121.65 (17)H28B—C28—H28C109.5
N1—C12—H12A114.4C15—C29—H29A109.5
C13—C12—H12A114.4C15—C29—H29B109.5
C8—C12—H12A114.4H29A—C29—H29B109.5
C12—C13—N155.96 (15)C15—C29—H29C109.5
C12—C13—C14121.46 (17)H29A—C29—H29C109.5
N1—C13—C14115.9 (2)H29B—C29—H29C109.5
C12—C13—H13A116.5C19—C30—H30A109.5
N1—C13—H13A116.5C19—C30—H30B109.5
C14—C13—H13A116.5H30A—C30—H30B109.5
C13—C14—C23109.54 (15)C19—C30—H30C109.5
C13—C14—C15114.15 (16)H30A—C30—H30C109.5
C23—C14—C15117.30 (15)H30B—C30—H30C109.5
C13—C14—H14A104.8C19—C31—H31A109.5
C23—C14—H14A104.8C19—C31—H31B109.5
C15—C14—H14A104.8H31A—C31—H31B109.5
C29—C15—C16107.99 (18)C19—C31—H31C109.5
C29—C15—C20115.13 (16)H31A—C31—H31C109.5
C16—C15—C20107.86 (17)H31B—C31—H31C109.5
C29—C15—C14113.26 (16)C23—C32—H32A109.5
C16—C15—C14107.20 (15)C23—C32—H32B109.5
C20—C15—C14105.03 (15)H32A—C32—H32B109.5
C17—C16—C15112.80 (15)C23—C32—H32C109.5
C17—C16—H16A109.0H32A—C32—H32C109.5
C15—C16—H16A109.0H32B—C32—H32C109.5
C17—C16—H16B109.0
C8—O1—C1—O4−178.70 (18)C12—N1—C13—C14−111.9 (2)
C8—O1—C1—C20.5 (2)C12—C13—C14—C2333.2 (3)
O4—C1—C2—C3−33.0 (3)N1—C13—C14—C2397.6 (2)
O1—C1—C2—C3147.89 (16)C12—C13—C14—C15167.0 (2)
O4—C1—C2—C7−151.4 (2)N1—C13—C14—C15−128.61 (18)
O1—C1—C2—C729.49 (19)C13—C14—C15—C29−58.5 (2)
O4—C1—C2—C1193.6 (2)C23—C14—C15—C2971.6 (2)
O1—C1—C2—C11−85.54 (19)C13—C14—C15—C1660.5 (2)
C1—C2—C3—C4−163.28 (17)C23—C14—C15—C16−169.39 (18)
C7—C2—C3—C4−51.7 (2)C13—C14—C15—C20175.07 (19)
C11—C2—C3—C473.6 (2)C23—C14—C15—C20−54.8 (2)
C2—C3—C4—C555.2 (2)C29—C15—C16—C17−72.5 (2)
C3—C4—C5—C27−174.19 (16)C20—C15—C16—C1752.5 (2)
C3—C4—C5—C2666.7 (2)C14—C15—C16—C17165.10 (18)
C3—C4—C5—C6−57.1 (2)C15—C16—C17—C18−57.9 (3)
C27—C5—C6—C7173.35 (17)C24—O2—C18—C17106.1 (2)
C26—C5—C6—C7−67.5 (2)C24—O2—C18—C19−129.18 (19)
C4—C5—C6—C755.8 (2)C16—C17—C18—O2−177.98 (17)
C5—C6—C7—C2−57.1 (2)C16—C17—C18—C1961.1 (2)
C5—C6—C7—C8−179.84 (18)O2—C18—C19—C31−52.2 (2)
C1—C2—C7—C6177.12 (15)C17—C18—C19—C3169.0 (2)
C3—C2—C7—C655.2 (2)O2—C18—C19—C3066.3 (2)
C11—C2—C7—C6−71.3 (2)C17—C18—C19—C30−172.55 (16)
C1—C2—C7—C8−46.17 (17)O2—C18—C19—C20−177.56 (17)
C3—C2—C7—C8−168.12 (18)C17—C18—C19—C20−56.4 (2)
C11—C2—C7—C865.4 (2)C29—C15—C20—C21−64.4 (2)
C1—O1—C8—C12−147.48 (15)C16—C15—C20—C21175.02 (16)
C1—O1—C8—C7−30.11 (18)C14—C15—C20—C2160.9 (2)
C1—O1—C8—C991.20 (17)C29—C15—C20—C1968.5 (2)
C6—C7—C8—O1175.33 (17)C16—C15—C20—C19−52.1 (2)
C2—C7—C8—O146.32 (17)C14—C15—C20—C19−166.21 (17)
C6—C7—C8—C12−75.3 (3)C18—C19—C20—C21−175.71 (18)
C2—C7—C8—C12155.67 (19)C31—C19—C20—C2160.4 (2)
C6—C7—C8—C960.2 (2)C30—C19—C20—C21−60.8 (2)
C2—C7—C8—C9−68.8 (2)C18—C19—C20—C1553.0 (2)
O1—C8—C9—C10−48.83 (19)C31—C19—C20—C15−71.0 (2)
C12—C8—C9—C10−163.63 (19)C30—C19—C20—C15167.88 (18)
C7—C8—C9—C1060.8 (2)C15—C20—C21—C22−64.6 (2)
O1—C8—C9—C28−165.30 (14)C19—C20—C21—C22160.85 (18)
C12—C8—C9—C2879.9 (2)C20—C21—C22—C2356.1 (2)
C7—C8—C9—C28−55.6 (2)C21—C22—C23—C3274.7 (2)
O1—C8—C9—C2373.13 (18)C21—C22—C23—C14−46.4 (2)
C12—C8—C9—C23−41.7 (2)C21—C22—C23—C9−162.63 (17)
C7—C8—C9—C23−177.21 (16)C13—C14—C23—C3262.1 (2)
C28—C9—C10—C1172.3 (2)C15—C14—C23—C32−70.1 (2)
C8—C9—C10—C11−45.8 (2)C13—C14—C23—C22−179.53 (19)
C23—C9—C10—C11−166.56 (18)C15—C14—C23—C2248.3 (2)
C9—C10—C11—C249.1 (3)C13—C14—C23—C9−60.5 (2)
C1—C2—C11—C1045.1 (2)C15—C14—C23—C9167.27 (17)
C3—C2—C11—C10173.17 (18)C10—C9—C23—C3263.8 (2)
C7—C2—C11—C10−61.6 (2)C28—C9—C23—C32−176.72 (16)
C13—N1—C12—C8113.1 (2)C8—C9—C23—C32−55.4 (2)
O1—C8—C12—N1179.68 (16)C10—C9—C23—C22−55.5 (2)
C7—C8—C12—N173.5 (2)C28—C9—C23—C2264.0 (2)
C9—C8—C12—N1−63.0 (2)C8—C9—C23—C22−174.65 (16)
O1—C8—C12—C13−105.2 (2)C10—C9—C23—C14−174.31 (17)
C7—C8—C12—C13148.7 (2)C28—C9—C23—C14−54.80 (19)
C9—C8—C12—C1312.1 (3)C8—C9—C23—C1466.6 (2)
C8—C12—C13—N1−109.5 (3)C18—O2—C24—O3−3.3 (3)
N1—C12—C13—C14101.7 (3)C18—O2—C24—C25176.38 (17)
C8—C12—C13—C14−7.8 (4)
  4 in total

1.  Isolation and bioactivities of constitutents of the roots of Garcinia atroviridis.

Authors:  D Permana; N H Lajis; M M Mackeen; A M Ali; N Aimi; M Kitajima; H Takayama
Journal:  J Nat Prod       Date:  2001-07       Impact factor: 4.050

2.  A short history of SHELX.

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

3.  Effects of Garcinia atroviridis on serum profiles and atherosclerotic lesions in the aorta of guinea pigs fed a high cholesterol diet.

Authors:  A A Amran; Z Zaiton; O Faizah; P Morat
Journal:  Singapore Med J       Date:  2009-03       Impact factor: 1.858

4.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  4 in total

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