Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807042535/wn2196sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807042535/wn2196Isup2.hkl |
CCDC reference: 663693
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.006 Å
- R factor = 0.062
- wR factor = 0.189
- Data-to-parameter ratio = 7.6
checkCIF/PLATON results
No syntax errors found
Alert level C GOODF01_ALERT_2_C The least squares goodness of fit parameter lies outside the range 0.80 <> 2.00 Goodness of fit given = 0.797 PLAT089_ALERT_3_C Poor Data / Parameter Ratio (Zmax .LT. 18) ..... 7.56 PLAT125_ALERT_4_C No _symmetry_space_group_name_Hall Given ....... ? PLAT180_ALERT_3_C Check Cell Rounding: # of Values Ending with 0 = 3 PLAT250_ALERT_2_C Large U3/U1 Ratio for Average U(i,j) Tensor .... 2.30 PLAT340_ALERT_3_C Low Bond Precision on C-C Bonds (x 1000) Ang ... 6 PLAT412_ALERT_2_C Short Intra XH3 .. XHn H19A .. H30C .. 1.80 Ang. PLAT601_ALERT_2_C Structure Contains Solvent Accessible VOIDS of . 48.00 A 3
Alert level G REFLT03_ALERT_4_G Please check that the estimate of the number of Friedel pairs is correct. If it is not, please give the correct count in the _publ_section_exptl_refinement section of the submitted CIF. From the CIF: _diffrn_reflns_theta_max 67.45 From the CIF: _reflns_number_total 2161 Count of symmetry unique reflns 2172 Completeness (_total/calc) 99.49% TEST3: Check Friedels for noncentro structure Estimate of Friedel pairs measured 0 Fraction of Friedel pairs measured 0.000 Are heavy atom types Z>Si present no PLAT199_ALERT_1_G Check the Reported _cell_measurement_temperature 293 K PLAT200_ALERT_1_G Check the Reported _diffrn_ambient_temperature . 293 K PLAT791_ALERT_1_G Confirm the Absolute Configuration of C8 = . R PLAT791_ALERT_1_G Confirm the Absolute Configuration of C9 = . R PLAT791_ALERT_1_G Confirm the Absolute Configuration of C10 = . R PLAT791_ALERT_1_G Confirm the Absolute Configuration of C13 = . S PLAT791_ALERT_1_G Confirm the Absolute Configuration of C14 = . R PLAT791_ALERT_1_G Confirm the Absolute Configuration of C15 = . R PLAT791_ALERT_1_G Confirm the Absolute Configuration of C17 = . S PLAT860_ALERT_3_G Note: Number of Least-Squares Restraints ....... 1
0 ALERT level A = In general: serious problem 0 ALERT level B = Potentially serious problem 8 ALERT level C = Check and explain 11 ALERT level G = General alerts; check 9 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 4 ALERT type 2 Indicator that the structure model may be wrong or deficient 4 ALERT type 3 Indicator that the structure quality may be low 2 ALERT type 4 Improvement, methodology, query or suggestion 0 ALERT type 5 Informative message, check
Many cedrelone derivatives have been reported (Hodges et al., 1963). The three-dimensional structure of cedrelone itself has previously been reported (Zeumer et al., 2000). For related literature, see: Bernstein et al. (1995); Cremer & Pople (1975); Narayanan et al. (1980).
Acetic acid (5 ml) was placed in a 25 ml Erylenmeyer flask fitted with microwave and reflux condenser with guard tube. To this cedrelone (141 mg, 0.33 mmol) and activated zinc was added. The mixture was then subjected to microwave radiation. After completion of the reaction, the solution was passed through a celite bed, followed by acetic acid and was removed by vacuum distillation. The title compound was purified by short flash (under nitrogen) column chromatography.
In the absence of significant anomalous scattering effects, 2161 Friedel equivalents were merged. The enantiomer employed in the refined model was chosen to agree with the accepted configuration of tetranortriterpenoids (Narayanan et al., 1980).
Hydrogen atoms were positioned geometrically and constrained to ride on their parent atoms, with C—H = 0.93, 0.96, 0.97 and 0.98 Å for Csp2, methyl, methylene and methine, respectively; O—H = 0.82 Å. These C—H and O—H bonds were allowed to rotate freely about the C—C and C—O bonds. Uiso(H) = xUeq(carrier atom) where x = 1.5 for methyl and O, 1.2 for all other H atoms.
A tetranortriterpenoid, cedrelone, has been previously isolated from Toona ciliata and its three dimensional structure was reported earlier (Zeumer et al., 2000). It possesses half the antifeedant activity of the most potent azadirachtin-A from Azadirachta indica. The title compound (Fig. 1), a semisynthetic derivative of cedrelone, differs from the parent molecule simply by having single bond C1—C2 rather than C1═C2. Except for ring A, the ring conformations in the title compound are the same as in cedrelone (Zeumer et al., 2000). The orientation of the furan ring is defined by the torsion angle C16—C17—C20—C22 = 179.8 (4)°; the corresponding value in cedrelone is 168.3 (4)°.
Ring A exists in a sofa conformation (Cremer & Pople, 1975) [QT = 0.688 (4) Å, φ2 = -48 (3)°, q2 = 0.677 (4) Å], and a mirror plane passes through atoms C3 and C10; in cedrelone itself, ring A adopts a distorted half-chair conformation. Ring B [QT =0.522 (4) Å, φ2=32.3 (5)°,q2 =0.435 (3) Å] adopts a half-chair conformation. Ring C adopts a twist conformation [QT =0.760 (3) Å, φ2 =88.1 (3) °, q2 =0.757 (3) Å]. The atoms C8 and C9 deviate from the mean plane of the other four atoms by 0.385 (3) Å and -0.407 (3) Å respectively. Ring D is in an envelope conformation [φ2 = -145.1 (3)°,q2 = 0.204 (4) Å] and ring E is planar (Nardelli, 1995). Ring pairs A/B, B/C and C/D are in quasi-trans fusion as evident from the endocyclic torsion angles of ring junction atoms. Thus, for rings A/B C4—C5—C10—C1 = -51.8 (4)° and C6—C5—C10—C9 = 9.8 (5)\5; for rings B/C C7—C8—C9—C10 = 63.5 (4)° and C14—C8—C9—C11 = -37.9 (4)°; for rings C/D C12—C13—C14—C8 = 58.5 (4)° and C17—C13—C14—C15 = -19.0 (4)°.
The packing of the molecules (Fig. 2) reveals that the crystal structure is stabilized by a network of hydrogen bonds (Table 1). The hydrogen bond C12—H12A···O15(-x+2,y+1/2,-z) forms an infinite chain, graph set motif C(9). A ring motif S(5) is formed by the hydrogen bond O6—H6···O7. In addition, R22(9) is generated through C2—H2A···O7(1+x,y,z) and O6—H6···O3(-1+x,y,z). All the observed hydrogen bonds in the crystal structure together form a macrocyclic ring motif R44(28).
Many cedrelone derivatives have been reported (Hodges et al., 1963). The three-dimensional structure of cedrelone itself has previously been reported (Zeumer et al., 2000). For related literature, see: Bernstein et al. (1995); Cremer & Pople (1975); Narayanan et al. (1980).
Data collection: CAD-4 EXPRESS (Enraf–Nonius, 1994); cell refinement: CAD-4 EXPRESS; data reduction: XCAD4 (Harms & Wocadlo, 1995); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEPIII (Burnett & Johnson, 1996); software used to prepare material for publication: SHELXL97 and PARST97 (Nardelli, 1995).
C26H32O5 | F(000) = 456 |
Mr = 424.52 | Dx = 1.239 Mg m−3 |
Monoclinic, P21 | Cu Kα radiation, λ = 1.54184 Å |
a = 8.302 (4) Å | Cell parameters from 25 reflections |
b = 10.150 (2) Å | θ = 15–30° |
c = 13.560 (5) Å | µ = 0.68 mm−1 |
β = 95.330 (3)° | T = 293 K |
V = 1137.7 (7) Å3 | Rod, colourless |
Z = 2 | 0.30 × 0.23 × 0.21 mm |
Enraf–Nonius CAD-4 diffractometer | Rint = 0.087 |
Radiation source: fine-focus sealed tube | θmax = 67.5°, θmin = 3.3° |
Graphite monochromator | h = 0→9 |
non–profiled ω/2θ scans | k = 0→12 |
2591 measured reflections | l = −16→16 |
2161 independent reflections | 3 standard reflections every 200 reflections |
1974 reflections with I > 2σ(I) | intensity decay: 3% |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.062 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.189 | H-atom parameters constrained |
S = 0.80 | w = 1/[σ2(Fo2) + (0.199P)2 + 0.4014P] where P = (Fo2 + 2Fc2)/3 |
2161 reflections | (Δ/σ)max < 0.001 |
286 parameters | Δρmax = 0.25 e Å−3 |
1 restraint | Δρmin = −0.34 e Å−3 |
C26H32O5 | V = 1137.7 (7) Å3 |
Mr = 424.52 | Z = 2 |
Monoclinic, P21 | Cu Kα radiation |
a = 8.302 (4) Å | µ = 0.68 mm−1 |
b = 10.150 (2) Å | T = 293 K |
c = 13.560 (5) Å | 0.30 × 0.23 × 0.21 mm |
β = 95.330 (3)° |
Enraf–Nonius CAD-4 diffractometer | Rint = 0.087 |
2591 measured reflections | 3 standard reflections every 200 reflections |
2161 independent reflections | intensity decay: 3% |
1974 reflections with I > 2σ(I) |
R[F2 > 2σ(F2)] = 0.062 | 1 restraint |
wR(F2) = 0.189 | H-atom parameters constrained |
S = 0.80 | Δρmax = 0.25 e Å−3 |
2161 reflections | Δρmin = −0.34 e Å−3 |
286 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
O3 | 1.5868 (3) | 0.4276 (5) | 0.4887 (2) | 0.0712 (11) | |
O6 | 0.9552 (3) | 0.3939 (4) | 0.4596 (2) | 0.0630 (9) | |
H6 | 0.8586 | 0.3758 | 0.4535 | 0.095* | |
O7 | 0.7759 (3) | 0.2519 (4) | 0.3276 (2) | 0.0597 (8) | |
O15 | 0.9023 (4) | −0.0169 (3) | 0.1327 (2) | 0.0562 (8) | |
O23 | 0.4733 (4) | 0.2782 (4) | −0.2042 (3) | 0.0756 (10) | |
C1 | 1.3541 (5) | 0.4167 (4) | 0.2475 (3) | 0.0504 (9) | |
H1A | 1.2753 | 0.4857 | 0.2312 | 0.060* | |
H1B | 1.3997 | 0.3917 | 0.1868 | 0.060* | |
C2 | 1.4901 (5) | 0.4715 (5) | 0.3212 (3) | 0.0552 (10) | |
H2A | 1.5929 | 0.4370 | 0.3043 | 0.066* | |
H2B | 1.4933 | 0.5666 | 0.3145 | 0.066* | |
C3 | 1.4699 (5) | 0.4379 (5) | 0.4265 (3) | 0.0543 (10) | |
C4 | 1.2979 (4) | 0.4246 (5) | 0.4560 (3) | 0.0538 (10) | |
C5 | 1.1889 (4) | 0.3489 (4) | 0.3773 (2) | 0.0426 (8) | |
C6 | 1.0297 (4) | 0.3354 (4) | 0.3850 (3) | 0.0471 (9) | |
C7 | 0.9206 (4) | 0.2529 (4) | 0.3168 (2) | 0.0444 (8) | |
C8 | 0.9996 (4) | 0.1674 (4) | 0.2466 (3) | 0.0414 (8) | |
C9 | 1.1337 (4) | 0.2540 (4) | 0.2070 (2) | 0.0402 (8) | |
H9 | 1.0782 | 0.3363 | 0.1871 | 0.048* | |
C10 | 1.2675 (4) | 0.2968 (4) | 0.2875 (2) | 0.0392 (7) | |
C11 | 1.1805 (4) | 0.1959 (5) | 0.1099 (2) | 0.0467 (8) | |
H11A | 1.2008 | 0.1022 | 0.1182 | 0.056* | |
H11B | 1.2792 | 0.2372 | 0.0923 | 0.056* | |
C12 | 1.0432 (4) | 0.2181 (5) | 0.0258 (3) | 0.0505 (9) | |
H12A | 1.0549 | 0.3052 | −0.0022 | 0.061* | |
H12B | 1.0538 | 0.1540 | −0.0262 | 0.061* | |
C13 | 0.8738 (4) | 0.2059 (4) | 0.0624 (3) | 0.0444 (8) | |
C14 | 0.8874 (4) | 0.1230 (4) | 0.1566 (3) | 0.0439 (8) | |
C15 | 0.7478 (5) | 0.0347 (5) | 0.1551 (3) | 0.0548 (10) | |
H15 | 0.7027 | 0.0105 | 0.2169 | 0.066* | |
C16 | 0.6376 (5) | 0.0597 (5) | 0.0623 (3) | 0.0610 (11) | |
H16A | 0.5500 | 0.1187 | 0.0752 | 0.073* | |
H16B | 0.5924 | −0.0219 | 0.0348 | 0.073* | |
C17 | 0.7501 (4) | 0.1237 (4) | −0.0076 (3) | 0.0493 (9) | |
H17 | 0.8114 | 0.0522 | −0.0351 | 0.059* | |
C18 | 0.7977 (5) | 0.3403 (4) | 0.0818 (3) | 0.0520 (9) | |
H18A | 0.7887 | 0.3912 | 0.0218 | 0.078* | |
H18B | 0.8646 | 0.3864 | 0.1320 | 0.078* | |
H18C | 0.6921 | 0.3274 | 0.1036 | 0.078* | |
C19 | 1.3932 (4) | 0.1871 (4) | 0.3153 (3) | 0.0486 (9) | |
H19A | 1.3399 | 0.1124 | 0.3410 | 0.073* | |
H19B | 1.4739 | 0.2196 | 0.3646 | 0.073* | |
H19C | 1.4438 | 0.1613 | 0.2574 | 0.073* | |
C20 | 0.6656 (5) | 0.1966 (5) | −0.0939 (3) | 0.0541 (9) | |
C21 | 0.5047 (5) | 0.2089 (7) | −0.1179 (3) | 0.0687 (13) | |
H21 | 0.4257 | 0.1748 | −0.0808 | 0.082* | |
C22 | 0.7396 (6) | 0.2648 (5) | −0.1704 (4) | 0.0666 (12) | |
H22 | 0.8499 | 0.2757 | −0.1747 | 0.080* | |
C23 | 0.6198 (7) | 0.3102 (5) | −0.2348 (4) | 0.0716 (14) | |
H23 | 0.6348 | 0.3569 | −0.2923 | 0.086* | |
C28 | 1.2986 (5) | 0.3573 (8) | 0.5571 (3) | 0.0775 (16) | |
H28A | 1.3600 | 0.4095 | 0.6063 | 0.116* | |
H28B | 1.3467 | 0.2716 | 0.5541 | 0.116* | |
H28C | 1.1895 | 0.3487 | 0.5743 | 0.116* | |
C29 | 1.2402 (6) | 0.5703 (6) | 0.4622 (5) | 0.0755 (15) | |
H29A | 1.2370 | 0.6102 | 0.3979 | 0.113* | |
H29B | 1.3140 | 0.6181 | 0.5077 | 0.113* | |
H29C | 1.1341 | 0.5723 | 0.4849 | 0.113* | |
C30 | 1.0586 (5) | 0.0445 (4) | 0.3070 (3) | 0.0511 (9) | |
H30A | 1.1104 | −0.0153 | 0.2651 | 0.077* | |
H30B | 0.9678 | 0.0016 | 0.3322 | 0.077* | |
H30C | 1.1342 | 0.0709 | 0.3613 | 0.077* |
U11 | U22 | U33 | U12 | U13 | U23 | |
O3 | 0.0370 (14) | 0.101 (3) | 0.0708 (18) | 0.0006 (17) | −0.0225 (13) | −0.0111 (19) |
O6 | 0.0343 (13) | 0.091 (2) | 0.0628 (16) | −0.0005 (15) | −0.0003 (11) | −0.0290 (16) |
O7 | 0.0232 (12) | 0.082 (2) | 0.0742 (17) | −0.0001 (14) | 0.0049 (10) | −0.0155 (16) |
O15 | 0.0564 (17) | 0.0424 (14) | 0.0668 (17) | −0.0008 (13) | −0.0096 (13) | −0.0048 (12) |
O23 | 0.0601 (19) | 0.075 (2) | 0.085 (2) | 0.0165 (18) | −0.0323 (16) | −0.0062 (19) |
C1 | 0.0315 (17) | 0.058 (2) | 0.060 (2) | −0.0098 (17) | −0.0086 (15) | 0.0033 (18) |
C2 | 0.0330 (18) | 0.058 (2) | 0.071 (2) | −0.0062 (18) | −0.0121 (15) | −0.002 (2) |
C3 | 0.0367 (19) | 0.062 (2) | 0.061 (2) | −0.0051 (18) | −0.0128 (15) | −0.0082 (19) |
C4 | 0.0306 (18) | 0.072 (3) | 0.055 (2) | 0.0025 (19) | −0.0158 (14) | −0.0133 (19) |
C5 | 0.0311 (16) | 0.0515 (19) | 0.0429 (16) | 0.0036 (16) | −0.0091 (12) | −0.0012 (15) |
C6 | 0.0336 (16) | 0.061 (2) | 0.0448 (16) | −0.0009 (17) | −0.0049 (12) | −0.0070 (16) |
C7 | 0.0284 (16) | 0.056 (2) | 0.0479 (17) | 0.0004 (16) | −0.0008 (12) | 0.0012 (16) |
C8 | 0.0255 (14) | 0.0461 (19) | 0.0511 (17) | −0.0025 (15) | −0.0043 (12) | −0.0021 (15) |
C9 | 0.0243 (15) | 0.0468 (18) | 0.0481 (16) | −0.0006 (15) | −0.0044 (12) | 0.0013 (15) |
C10 | 0.0260 (14) | 0.0438 (17) | 0.0461 (16) | 0.0030 (14) | −0.0062 (12) | 0.0007 (14) |
C11 | 0.0301 (15) | 0.061 (2) | 0.0483 (17) | −0.0009 (17) | −0.0027 (13) | −0.0041 (17) |
C12 | 0.0378 (18) | 0.064 (2) | 0.0475 (18) | −0.0063 (18) | −0.0073 (13) | 0.0010 (17) |
C13 | 0.0336 (17) | 0.0467 (18) | 0.0504 (17) | −0.0047 (15) | −0.0093 (13) | −0.0034 (16) |
C14 | 0.0288 (16) | 0.0430 (19) | 0.058 (2) | −0.0015 (15) | −0.0051 (13) | −0.0040 (16) |
C15 | 0.0432 (19) | 0.059 (2) | 0.060 (2) | −0.021 (2) | −0.0044 (15) | −0.0022 (19) |
C16 | 0.046 (2) | 0.065 (3) | 0.069 (2) | −0.014 (2) | −0.0117 (17) | −0.009 (2) |
C17 | 0.0391 (19) | 0.051 (2) | 0.0547 (19) | −0.0077 (17) | −0.0134 (14) | −0.0054 (17) |
C18 | 0.0413 (19) | 0.0432 (19) | 0.067 (2) | −0.0006 (17) | −0.0164 (15) | −0.0061 (18) |
C19 | 0.0234 (15) | 0.056 (2) | 0.064 (2) | 0.0078 (16) | −0.0068 (13) | 0.0006 (18) |
C20 | 0.0399 (19) | 0.053 (2) | 0.065 (2) | 0.0002 (18) | −0.0192 (16) | −0.0077 (19) |
C21 | 0.042 (2) | 0.091 (4) | 0.069 (2) | 0.010 (2) | −0.0145 (17) | −0.009 (3) |
C22 | 0.056 (2) | 0.062 (3) | 0.076 (3) | −0.009 (2) | −0.025 (2) | 0.013 (2) |
C23 | 0.074 (3) | 0.054 (2) | 0.079 (3) | −0.007 (2) | −0.035 (2) | 0.012 (2) |
C28 | 0.047 (2) | 0.126 (5) | 0.056 (2) | 0.001 (3) | −0.0131 (17) | −0.003 (3) |
C29 | 0.049 (2) | 0.075 (3) | 0.099 (3) | −0.002 (2) | −0.008 (2) | −0.036 (3) |
C30 | 0.0405 (18) | 0.050 (2) | 0.061 (2) | −0.0072 (18) | −0.0040 (15) | 0.0051 (18) |
O3—C3 | 1.230 (5) | C12—H12A | 0.9700 |
O6—C6 | 1.369 (5) | C12—H12B | 0.9700 |
O6—H6 | 0.8200 | C13—C14 | 1.525 (5) |
O7—C7 | 1.223 (4) | C13—C18 | 1.537 (6) |
O15—C15 | 1.444 (6) | C13—C17 | 1.572 (5) |
O15—C14 | 1.465 (5) | C14—C15 | 1.464 (5) |
O23—C23 | 1.360 (7) | C15—C16 | 1.507 (6) |
O23—C21 | 1.370 (6) | C15—H15 | 0.9800 |
C1—C10 | 1.538 (5) | C16—C17 | 1.535 (6) |
C1—C2 | 1.541 (5) | C16—H16A | 0.9700 |
C1—H1A | 0.9700 | C16—H16B | 0.9700 |
C1—H1B | 0.9700 | C17—C20 | 1.502 (5) |
C2—C3 | 1.491 (6) | C17—H17 | 0.9800 |
C2—H2A | 0.9700 | C18—H18A | 0.9600 |
C2—H2B | 0.9700 | C18—H18B | 0.9600 |
C3—C4 | 1.524 (6) | C18—H18C | 0.9600 |
C4—C28 | 1.531 (7) | C19—H19A | 0.9600 |
C4—C5 | 1.538 (5) | C19—H19B | 0.9600 |
C4—C29 | 1.559 (8) | C19—H19C | 0.9600 |
C5—C6 | 1.343 (5) | C20—C21 | 1.351 (6) |
C5—C10 | 1.529 (5) | C20—C22 | 1.433 (7) |
C6—C7 | 1.491 (5) | C21—H21 | 0.9300 |
C7—O7 | 1.223 (4) | C22—C23 | 1.342 (6) |
C7—C8 | 1.486 (5) | C22—H22 | 0.9300 |
C8—C14 | 1.532 (5) | C23—H23 | 0.9300 |
C8—C30 | 1.548 (5) | C28—H28A | 0.9600 |
C8—C9 | 1.553 (5) | C28—H28B | 0.9600 |
C9—C11 | 1.525 (5) | C28—H28C | 0.9600 |
C9—C10 | 1.546 (4) | C29—H29A | 0.9600 |
C9—H9 | 0.9800 | C29—H29B | 0.9600 |
C10—C19 | 1.548 (5) | C29—H29C | 0.9600 |
C11—C12 | 1.552 (5) | C30—H30A | 0.9600 |
C11—H11A | 0.9700 | C30—H30B | 0.9600 |
C11—H11B | 0.9700 | C30—H30C | 0.9600 |
C12—C13 | 1.539 (5) | ||
C6—O6—H6 | 109.5 | C12—C13—C17 | 114.4 (3) |
C15—O15—C14 | 60.4 (3) | C15—C14—O15 | 59.1 (3) |
C23—O23—C21 | 106.2 (3) | C15—C14—C13 | 109.2 (3) |
C10—C1—C2 | 113.3 (3) | O15—C14—C13 | 110.5 (3) |
C10—C1—H1A | 108.9 | C15—C14—C8 | 127.9 (3) |
C2—C1—H1A | 108.9 | O15—C14—C8 | 113.8 (3) |
C10—C1—H1B | 108.9 | C13—C14—C8 | 119.8 (3) |
C2—C1—H1B | 108.9 | O15—C15—C14 | 60.5 (2) |
H1A—C1—H1B | 107.7 | O15—C15—C16 | 111.6 (3) |
C3—C2—C1 | 113.4 (3) | C14—C15—C16 | 109.1 (4) |
C3—C2—H2A | 108.9 | O15—C15—H15 | 120.4 |
C1—C2—H2A | 108.9 | C14—C15—H15 | 120.4 |
C3—C2—H2B | 108.9 | C16—C15—H15 | 120.4 |
C1—C2—H2B | 108.9 | C15—C16—C17 | 103.3 (3) |
H2A—C2—H2B | 107.7 | C15—C16—H16A | 111.1 |
O3—C3—C2 | 121.6 (4) | C17—C16—H16A | 111.1 |
O3—C3—C4 | 120.7 (4) | C15—C16—H16B | 111.1 |
C2—C3—C4 | 117.6 (3) | C17—C16—H16B | 111.1 |
C3—C4—C28 | 110.4 (3) | H16A—C16—H16B | 109.1 |
C3—C4—C5 | 111.5 (3) | C20—C17—C16 | 115.0 (3) |
C28—C4—C5 | 110.5 (4) | C20—C17—C13 | 116.2 (3) |
C3—C4—C29 | 103.3 (4) | C16—C17—C13 | 104.6 (3) |
C28—C4—C29 | 110.5 (5) | C20—C17—H17 | 106.8 |
C5—C4—C29 | 110.3 (3) | C16—C17—H17 | 106.8 |
C6—C5—C10 | 121.5 (3) | C13—C17—H17 | 106.8 |
C6—C5—C4 | 121.1 (3) | C13—C18—H18A | 109.5 |
C10—C5—C4 | 117.3 (3) | C13—C18—H18B | 109.5 |
C5—C6—O6 | 121.9 (3) | H18A—C18—H18B | 109.5 |
C5—C6—C7 | 123.7 (3) | C13—C18—H18C | 109.5 |
O6—C6—C7 | 114.3 (3) | H18A—C18—H18C | 109.5 |
O7—C7—C8 | 124.6 (3) | H18B—C18—H18C | 109.5 |
O7—C7—C6 | 118.5 (3) | C10—C19—H19A | 109.5 |
C8—C7—C6 | 116.6 (3) | C10—C19—H19B | 109.5 |
C7—C8—C14 | 114.2 (3) | H19A—C19—H19B | 109.5 |
C7—C8—C30 | 105.5 (3) | C10—C19—H19C | 109.5 |
C14—C8—C30 | 108.9 (3) | H19A—C19—H19C | 109.5 |
C7—C8—C9 | 105.3 (3) | H19B—C19—H19C | 109.5 |
C14—C8—C9 | 107.1 (3) | C21—C20—C22 | 105.1 (4) |
C30—C8—C9 | 115.9 (3) | C21—C20—C17 | 127.8 (4) |
C11—C9—C10 | 119.6 (3) | C22—C20—C17 | 127.0 (4) |
C11—C9—C8 | 109.1 (3) | C20—C21—O23 | 111.0 (5) |
C10—C9—C8 | 114.0 (3) | C20—C21—H21 | 124.5 |
C11—C9—H9 | 104.1 | O23—C21—H21 | 124.5 |
C10—C9—H9 | 104.1 | C23—C22—C20 | 107.2 (4) |
C8—C9—H9 | 104.1 | C23—C22—H22 | 126.4 |
C5—C10—C1 | 104.8 (3) | C20—C22—H22 | 126.4 |
C5—C10—C9 | 109.1 (2) | C22—C23—O23 | 110.4 (5) |
C1—C10—C9 | 107.6 (3) | C22—C23—H23 | 124.8 |
C5—C10—C19 | 112.5 (3) | O23—C23—H23 | 124.8 |
C1—C10—C19 | 109.2 (3) | C4—C28—H28A | 109.5 |
C9—C10—C19 | 113.2 (3) | C4—C28—H28B | 109.5 |
C9—C11—C12 | 110.5 (3) | H28A—C28—H28B | 109.5 |
C9—C11—H11A | 109.6 | C4—C28—H28C | 109.5 |
C12—C11—H11A | 109.6 | H28A—C28—H28C | 109.5 |
C9—C11—H11B | 109.6 | H28B—C28—H28C | 109.5 |
C12—C11—H11B | 109.6 | C4—C29—H29A | 109.5 |
H11A—C11—H11B | 108.1 | C4—C29—H29B | 109.5 |
C13—C12—C11 | 112.4 (3) | H29A—C29—H29B | 109.5 |
C13—C12—H12A | 109.1 | C4—C29—H29C | 109.5 |
C11—C12—H12A | 109.1 | H29A—C29—H29C | 109.5 |
C13—C12—H12B | 109.1 | H29B—C29—H29C | 109.5 |
C11—C12—H12B | 109.1 | C8—C30—H30A | 109.5 |
H12A—C12—H12B | 107.8 | C8—C30—H30B | 109.5 |
C14—C13—C18 | 110.3 (3) | H30A—C30—H30B | 109.5 |
C14—C13—C12 | 108.4 (3) | C8—C30—H30C | 109.5 |
C18—C13—C12 | 112.7 (3) | H30A—C30—H30C | 109.5 |
C14—C13—C17 | 101.9 (3) | H30B—C30—H30C | 109.5 |
C18—C13—C17 | 108.6 (3) | ||
C10—C1—C2—C3 | −23.4 (5) | C9—C11—C12—C13 | −36.7 (5) |
C1—C2—C3—O3 | 152.0 (5) | C11—C12—C13—C14 | −22.8 (5) |
C1—C2—C3—C4 | −31.6 (6) | C11—C12—C13—C18 | 99.6 (4) |
O3—C3—C4—C28 | −17.6 (7) | C11—C12—C13—C17 | −135.7 (4) |
C2—C3—C4—C28 | 165.9 (5) | C15—O15—C14—C13 | −100.7 (3) |
O3—C3—C4—C5 | −141.0 (5) | C15—O15—C14—C8 | 121.2 (4) |
C2—C3—C4—C5 | 42.5 (6) | C18—C13—C14—C15 | 96.1 (4) |
O3—C3—C4—C29 | 100.5 (5) | C12—C13—C14—C15 | −140.0 (3) |
C2—C3—C4—C29 | −76.0 (5) | C17—C13—C14—C15 | −19.0 (4) |
C3—C4—C5—C6 | −174.6 (4) | C18—C13—C14—O15 | 159.3 (3) |
C28—C4—C5—C6 | 62.1 (5) | C12—C13—C14—O15 | −76.8 (4) |
C29—C4—C5—C6 | −60.4 (6) | C17—C13—C14—O15 | 44.2 (4) |
C3—C4—C5—C10 | 2.0 (5) | C18—C13—C14—C8 | −65.3 (4) |
C28—C4—C5—C10 | −121.3 (4) | C12—C13—C14—C8 | 58.5 (4) |
C29—C4—C5—C10 | 116.2 (4) | C17—C13—C14—C8 | 179.5 (3) |
C10—C5—C6—O6 | −172.9 (4) | C7—C8—C14—C15 | −67.0 (5) |
C4—C5—C6—O6 | 3.6 (6) | C30—C8—C14—C15 | 50.7 (5) |
C10—C5—C6—C7 | 9.5 (6) | C9—C8—C14—C15 | 176.8 (4) |
C4—C5—C6—C7 | −174.0 (4) | C7—C8—C14—O15 | −135.4 (4) |
C5—C6—C7—O7 | −176.8 (4) | C30—C8—C14—O15 | −17.7 (4) |
O6—C6—C7—O7 | 5.5 (6) | C9—C8—C14—O15 | 108.4 (4) |
C5—C6—C7—C8 | 9.0 (6) | C7—C8—C14—C13 | 90.6 (4) |
O6—C6—C7—C8 | −168.8 (4) | C30—C8—C14—C13 | −151.7 (3) |
O7—C7—C8—C14 | 26.4 (5) | C9—C8—C14—C13 | −25.6 (4) |
C6—C7—C8—C14 | −159.7 (3) | C14—O15—C15—C16 | 100.4 (4) |
O7—C7—C8—C30 | −93.2 (4) | C13—C14—C15—O15 | 103.0 (3) |
C6—C7—C8—C30 | 80.7 (4) | C8—C14—C15—O15 | −97.5 (4) |
O7—C7—C8—C9 | 143.6 (4) | O15—C14—C15—C16 | −104.6 (4) |
C6—C7—C8—C9 | −42.5 (4) | C13—C14—C15—C16 | −1.6 (5) |
C7—C8—C9—C11 | −159.9 (3) | C8—C14—C15—C16 | 157.9 (4) |
C14—C8—C9—C11 | −37.9 (4) | O15—C15—C16—C17 | −42.8 (5) |
C30—C8—C9—C11 | 83.8 (4) | C14—C15—C16—C17 | 22.2 (5) |
C7—C8—C9—C10 | 63.5 (4) | C15—C16—C17—C20 | −162.2 (4) |
C14—C8—C9—C10 | −174.6 (3) | C15—C16—C17—C13 | −33.5 (5) |
C30—C8—C9—C10 | −52.8 (4) | C14—C13—C17—C20 | 160.1 (3) |
C6—C5—C10—C1 | 124.8 (4) | C18—C13—C17—C20 | 43.8 (4) |
C4—C5—C10—C1 | −51.8 (4) | C12—C13—C17—C20 | −83.1 (5) |
C6—C5—C10—C9 | 9.8 (5) | C14—C13—C17—C16 | 32.2 (4) |
C4—C5—C10—C9 | −166.8 (3) | C18—C13—C17—C16 | −84.1 (4) |
C6—C5—C10—C19 | −116.7 (4) | C12—C13—C17—C16 | 149.0 (4) |
C4—C5—C10—C19 | 66.7 (4) | C16—C17—C20—C21 | −1.9 (7) |
C2—C1—C10—C5 | 63.1 (4) | C13—C17—C20—C21 | −124.5 (5) |
C2—C1—C10—C9 | 179.2 (3) | C16—C17—C20—C22 | −179.8 (4) |
C2—C1—C10—C19 | −57.6 (4) | C13—C17—C20—C22 | 57.6 (6) |
C11—C9—C10—C5 | −179.0 (3) | C22—C20—C21—O23 | 0.8 (6) |
C8—C9—C10—C5 | −47.3 (4) | C17—C20—C21—O23 | −177.5 (4) |
C11—C9—C10—C1 | 67.8 (4) | C23—O23—C21—C20 | −0.1 (6) |
C8—C9—C10—C1 | −160.4 (3) | C21—C20—C22—C23 | −1.2 (6) |
C11—C9—C10—C19 | −52.8 (4) | C17—C20—C22—C23 | 177.1 (4) |
C8—C9—C10—C19 | 78.9 (4) | C20—C22—C23—O23 | 1.2 (6) |
C10—C9—C11—C12 | −154.6 (3) | C21—O23—C23—C22 | −0.7 (6) |
C8—C9—C11—C12 | 71.6 (4) |
D—H···A | D—H | H···A | D···A | D—H···A |
O6—H6···O3i | 0.82 | 2.41 | 3.139 (4) | 149 |
C12—H12A···O15ii | 0.97 | 2.58 | 3.499 (5) | 159 |
C2—H2A···O7iii | 0.97 | 2.42 | 3.251 (6) | 144 |
O6—H6···O7 | 0.82 | 2.18 | 2.646 (4) | 116 |
Symmetry codes: (i) x−1, y, z; (ii) −x+2, y+1/2, −z; (iii) x+1, y, z. |
Experimental details
Crystal data | |
Chemical formula | C26H32O5 |
Mr | 424.52 |
Crystal system, space group | Monoclinic, P21 |
Temperature (K) | 293 |
a, b, c (Å) | 8.302 (4), 10.150 (2), 13.560 (5) |
β (°) | 95.330 (3) |
V (Å3) | 1137.7 (7) |
Z | 2 |
Radiation type | Cu Kα |
µ (mm−1) | 0.68 |
Crystal size (mm) | 0.30 × 0.23 × 0.21 |
Data collection | |
Diffractometer | Enraf–Nonius CAD-4 |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 2591, 2161, 1974 |
Rint | 0.087 |
(sin θ/λ)max (Å−1) | 0.599 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.062, 0.189, 0.80 |
No. of reflections | 2161 |
No. of parameters | 286 |
No. of restraints | 1 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.25, −0.34 |
Computer programs: CAD-4 EXPRESS (Enraf–Nonius, 1994), CAD-4 EXPRESS, XCAD4 (Harms & Wocadlo, 1995), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), ORTEPIII (Burnett & Johnson, 1996), SHELXL97 and PARST97 (Nardelli, 1995).
D—H···A | D—H | H···A | D···A | D—H···A |
O6—H6···O3i | 0.82 | 2.41 | 3.139 (4) | 149.1 |
C12—H12A···O15ii | 0.97 | 2.58 | 3.499 (5) | 158.9 |
C2—H2A···O7iii | 0.97 | 2.42 | 3.251 (6) | 143.7 |
O6—H6···O7 | 0.82 | 2.18 | 2.646 (4) | 116.2 |
Symmetry codes: (i) x−1, y, z; (ii) −x+2, y+1/2, −z; (iii) x+1, y, z. |
Subscribe to Acta Crystallographica Section E: Crystallographic Communications
The full text of this article is available to subscribers to the journal.
- Information on subscribing
- Sample issue
- If you have already subscribed, you may need to register
A tetranortriterpenoid, cedrelone, has been previously isolated from Toona ciliata and its three dimensional structure was reported earlier (Zeumer et al., 2000). It possesses half the antifeedant activity of the most potent azadirachtin-A from Azadirachta indica. The title compound (Fig. 1), a semisynthetic derivative of cedrelone, differs from the parent molecule simply by having single bond C1—C2 rather than C1═C2. Except for ring A, the ring conformations in the title compound are the same as in cedrelone (Zeumer et al., 2000). The orientation of the furan ring is defined by the torsion angle C16—C17—C20—C22 = 179.8 (4)°; the corresponding value in cedrelone is 168.3 (4)°.
Ring A exists in a sofa conformation (Cremer & Pople, 1975) [QT = 0.688 (4) Å, φ2 = -48 (3)°, q2 = 0.677 (4) Å], and a mirror plane passes through atoms C3 and C10; in cedrelone itself, ring A adopts a distorted half-chair conformation. Ring B [QT =0.522 (4) Å, φ2=32.3 (5)°,q2 =0.435 (3) Å] adopts a half-chair conformation. Ring C adopts a twist conformation [QT =0.760 (3) Å, φ2 =88.1 (3) °, q2 =0.757 (3) Å]. The atoms C8 and C9 deviate from the mean plane of the other four atoms by 0.385 (3) Å and -0.407 (3) Å respectively. Ring D is in an envelope conformation [φ2 = -145.1 (3)°,q2 = 0.204 (4) Å] and ring E is planar (Nardelli, 1995). Ring pairs A/B, B/C and C/D are in quasi-trans fusion as evident from the endocyclic torsion angles of ring junction atoms. Thus, for rings A/B C4—C5—C10—C1 = -51.8 (4)° and C6—C5—C10—C9 = 9.8 (5)\5; for rings B/C C7—C8—C9—C10 = 63.5 (4)° and C14—C8—C9—C11 = -37.9 (4)°; for rings C/D C12—C13—C14—C8 = 58.5 (4)° and C17—C13—C14—C15 = -19.0 (4)°.
The packing of the molecules (Fig. 2) reveals that the crystal structure is stabilized by a network of hydrogen bonds (Table 1). The hydrogen bond C12—H12A···O15(-x+2,y+1/2,-z) forms an infinite chain, graph set motif C(9). A ring motif S(5) is formed by the hydrogen bond O6—H6···O7. In addition, R22(9) is generated through C2—H2A···O7(1+x,y,z) and O6—H6···O3(-1+x,y,z). All the observed hydrogen bonds in the crystal structure together form a macrocyclic ring motif R44(28).