6α-Acetoxy­gedunin

Hofer, M.; Greger, H.; Mereiter, K.

doi:10.1107/S1600536809027998

6α-Acetoxygedunin

The title compound [systematic name: (1S,3aS,4aR,4bS,5S,6R,6aR,10aR,10bR,12aS)-5,6-bis(acetyloxy)-1-(3-furyl)-1,5,6,6a,7,10a,10b,11,12,12a-decahydro-4b,7,7,10a,12a-pentamethyloxireno[c]phenanthro[1,2-d]pyran-3,8(3aH,4bH)-dione], C₃₀H₃₆O₉, is a limonoid-type triterpene isolated from Aglaia elaeagnoidea (A. Juss.) Benth. (Meliaceae) from Queensland, northern Australia. It contains the gedunin core of four trans-fused six-membered rings with an oxirane ring annelated to the fourth ring. A terminal 3-furyl unity and two acetoxy groups in a mutual cis-disposition supplement the molecule. A comparison between the gedunin cores of the title compound, the parent compound gedunin, and three further gedunin derivatives revealed considerable variations in their conformation stemming from the conformational lability of the first screw-boat ring and the third twist-boat ring. A sensitive measure for the third ring is one C—C—C—C torsion angle, which is 14.2 (2)° in the title compound, but varies in other cases from ca 20 to ca −40°. In the crystalline state, 6α-acetoxygedunin shows ten comparatively weak C—H

O interactions, with H

O distances in the range of 2.33–2.69 Å.

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Supporting information

	Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536809027998/fj2239sup1.cif Contains datablocks global, I
	Structure factor file (CIF format) https://doi.org/10.1107/S1600536809027998/fj2239Isup2.hkl Contains datablock I

CCDC reference: 744442

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Key indicators

Single-crystal X-ray study
T = 173 K
Mean (C-C) = 0.003 Å
R factor = 0.037
wR factor = 0.099
Data-to-parameter ratio = 12.6

checkCIF/PLATON results

No syntax errors found



Alert level A
PLAT220_ALERT_2_A Large Non-Solvent    O     Ueq(max)/Ueq(min) ...       4.68 Ratio

Author Response: ... Despite the use of low temperature X-ray diffraction, the furan ring C23-C24-C25-O7-C26 exhibits significant anisotropic displacement within the ring plane, with a point on the C17-C23 single bond as centroid of rotation. This is not unusual with complex compounds of natural origin. Attempts to describe this by a splitting of the furan ring in two orientations did not bring about any benefits for the present problem. The C-level Alerts PLAT220_ALERT_2_B Large Non-Solvent C Ueq(max)/Ueq(min) ... 4.42 Ratio PLAT230_ALERT_2_C Hirshfeld Test Diff for O8 - C27 .. 5.30 su stem also from the furan ring. Final remark to this problem: Compounds with this kind of natural source almost always lack sufficient material. In view of the available few milligrams of this rare compound, it was outstanding to obtain a reasonable crystal of 0.62 x 0.40 x 0.25 mm size.


Alert level B
PLAT220_ALERT_2_B Large Non-Solvent    C     Ueq(max)/Ueq(min) ...       4.42 Ratio

PLAT222_ALERT_3_B Large Non-Solvent    H     Ueq(max)/Ueq(min) ...       4.20 Ratio
PLAT063_ALERT_4_B Crystal Size Likely too Large for Beam Size ....       0.62 mm

Author Response: A beam with 0.8 mm nominal diameter was used (Bruker SMART platform 3-axis diffractometer).


Alert level C
PLAT230_ALERT_2_C Hirshfeld Test Diff for    O8     --  C27     ..       5.30 su
PLAT241_ALERT_2_C Check High      Ueq as Compared to Neighbors for         O7
PLAT412_ALERT_2_C Short Intra XH3 .. XHn     H9     ..  H18A    ..       1.86 Ang.

Author Response: CH3 groups refined in orientation with AFIX 137. These short H...H contacts are not unusual for this type of compound, they are mainly due to steric crowd.

PLAT412_ALERT_2_C Short Intra XH3 .. XHn     H19B   ..  H26A    ..       1.88 Ang.

Author Response: CH3 groups refined in orientation with AFIX 137. These short H...H contacts are not unusual for this type of compound, they are mainly due to steric crowd.

PLAT480_ALERT_4_C Long H...A H-Bond Reported H18C   ..  O1      ..       2.68 Ang.
PLAT480_ALERT_4_C Long H...A H-Bond Reported H22    ..  O6      ..       2.69 Ang.

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           29.98
           From the CIF: _reflns_number_total               4509
           Count of symmetry unique reflns         4558
           Completeness (_total/calc)             98.92%
           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
PLAT791_ALERT_4_G The Model has Chirality at C5      (Verify) ....          R
PLAT791_ALERT_4_G The Model has Chirality at C6      (Verify) ....          R
PLAT791_ALERT_4_G The Model has Chirality at C7      (Verify) ....          S
PLAT791_ALERT_4_G The Model has Chirality at C8      (Verify) ....          S
PLAT791_ALERT_4_G The Model has Chirality at C9      (Verify) ....          R
PLAT791_ALERT_4_G The Model has Chirality at C10     (Verify) ....          R
PLAT791_ALERT_4_G The Model has Chirality at C13     (Verify) ....          S
PLAT791_ALERT_4_G The Model has Chirality at C14     (Verify) ....          R
PLAT791_ALERT_4_G The Model has Chirality at C15     (Verify) ....          S
PLAT791_ALERT_4_G The Model has Chirality at C17     (Verify) ....          S

   1 ALERT level A = In general: serious problem
   3 ALERT level B = Potentially serious problem
   6 ALERT level C = Check and explain
  11 ALERT level G = General alerts; check

   0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
   6 ALERT type 2 Indicator that the structure model may be wrong or deficient
   1 ALERT type 3 Indicator that the structure quality may be low
  14 ALERT type 4 Improvement, methodology, query or suggestion
   0 ALERT type 5 Informative message, check

Comment top

The genus Aglaia of the family Meliaceae has received scientific attention due to its bioactivity potential. Besides its unique chemical capacity to produce flavaglines with pronounced insecticidal, antifungal, and anticancer activities (Greger et al., 2001; Engelmeier et al., 2000; Hausott et al., 2004), Aglaia is also characterized by the accumulation of bisamides, lignans, and triterpenes (Greger et al., 2000). However, in contrast to other genera of that family the highly active triterpenoid limonoids appear to be rare in Aglaia only known so far from Aglaia elaeagnoidea collected in Sempu Island, Java, Indonesia (6α,11β-diacetoxygedunin; Fuzzati et al., 1996), but not from samples collected in India and Thailand (Brader et al., 1998). Our investigation of the root bark of Aglaia elaeagnoidea originating from northern Australia led now to the second isolation of a limonoid from this genus, namely the title compound 6α-acetoxygedunin. This compound was previously isolated from several other genera of the Meliaceae family, such as Guarea grandiflora Decne.ex Steud. (Jimenez et al., 1998) or Carapa guianensis Aubl. (Lavie et al., 1972), but its crystal structure has not been determined as yet.

6α-Acetoxygedunin contains the gedunin skeleton with four six-membered rings (A, B, C, D), which are all trans-fused and adopt screw-boat, chair, twist-boat, and twisted half-chair conformation, respectively (Fig. 1). The D-ring, a lactone, is stiffened by fusion with an oxiran ring and bears in equatorial position a furan ring in approximately perpendicular orientation to the main plane of the molecule. Bond length and angles are normal (cf. geometric parameters) and compare well with the parent compound gedunin (Toscano et al., 1996), which is devoid of the 6-acetoxy group O2—(C27O8)—C28H₃, and with three more gedunin derivatives, 11α-hydroxygedunin (Mitsui et al., 2006), 11β-hydroxygedunin (Mitsui et al., 2006), and 7-oxogedunin (Waratchareeyakul et al., 2004; 7-acetoxy group replaced by a carbonyl oxygen with concomitant change of C7 from sp³ to sp² hybridization). However, the torsion angles within the A/B/C/D rings of these five compounds show in part considerable variations and consequently the molecular conformations as well. This is visualized by three superposition plots of 6α-acetoxygedunin and its congeners shown in Figures 2 to 4. Fig. 2 demonstrates that 6α-acetoxygedunin and 11α-hydroxygedunin (Mitsui et al. 2006; it contains two independent molecules) have relatively closely matching conformations of their A/B/C/D rings. Fig. 3 compares 6α-acetoxygedunin and gedunin showing that their B, C, and D rings match very well, but that the A-rings display a significant mismatch. The torsion angle T1 = C3—C4—C5—C10 may be used as a qualitative measure for this match/mismatch: It is 30.7 (2)° in 6α-acetoxygedunin and 51.2° in gedunin, while the remaining three gedunin-type compounds have T1 angles between 32.2° (11α-hydroxygedunin) and 45.3° (7-oxogedunin). Fig. 4 demonstrates that the most outstanding difference in conformation exists between 6α-acetoxygedunin and 7-oxogedunin. This difference does not arise from the unlike hybridization of C7 (sp³ in title compound and sp² in 7-oxogedunin), but is clearly provoked by ring C, which switches from a twist-boat conformation in 6α-acetoxygedunin via a virtual boat-intermediate into a twist-boat conformation of opposite twist in 7-oxogedunin. This can be tracked by the torsion angle T2 = C9—C11—C12—C13, which is +14.2 (2)° in 6α-acetoxygedunin (+21.6° in gedunin; +9.5° and +14.5° for the two independent molecules in 11α-hydroxygedunin), while it is -38.9° in 7-oxogedunin and -20.7° in 11β-hydroxygedunin. The described variations come essentially from the fact that B– and D-rings behave hard (B-ring in a relaxed and essentially invariant chair-conformation, D-ring in a twisted half-chair conformation fixed by oxiran ring and lacton group) while A-rings (screw-boat) and C-rings (between boat and twist-boat) behave soft and labile in conformation. The soft parts of the molecules are certainly controlled by the steric requirements of the ring substituents and by the crystal packing with its interplay of intra- and intermolecular forces. In the title compound 6α-acetoxygedunin such forces involve only several quite weak intra- and inter-molecular C—H···O interactions, which are listed in Table 1. For a packing diagram of 6α-acetoxygedunin, see Fig. 5.

Related literature top

For general background to the genus Aglaia and its potential bioctivity, see: Brader et al. (1998); Engelmeier et al. (2000); Fuzzati et al. (1996); Greger et al. (2000, 2001); Hausott et al. (2004); Jimenez et al. (1998); Lavie et al. (1972). For related structures, see: Mitsui et al. (2006); Sutherland et al. (1962); Toscano et al. (1996); Waratchareeyakul et al. (2004). For the NMR spectra of related compounds, see: Connolly et al. (1966); Mitsui et al. (2006); Taylor (1974); Waratchareeyakul et al. (2004).

Experimental top

Air-dried root bark of Aglaia elaeagnoidea (28 g) collected at the shore near Port Douglas, Queensland, northern Australia, was ground and extracted with MeOH at room temperature for 3 days, filtered and concentrated. The CHCl₃ fraction (1.2 g) of the aqueous residue was roughly separated by column chromatography (Merck Si gel 60, 35–70 mesh) eluted initially with hexane enriched with EtOAc, followed by an increasing amount of MeOH in EtOAc and finally with MeOH. The fraction eluted with 50% EtOAc in hexane was further separated by repeated preparative MPLC (400 x 40 mm column, Merck LiChroprep silica 60, 25–40 µm, UV detection at 229 and 254 nm) using 5% 2-propanol in hexane yielding 15 mg of impure 6α-acetoxygedunin from which 3.8 mg of crystals could be obtained.

The resonances of the ¹H and ¹³C NMR spectra of the title compound were assigned by two-dimensional NMR (H/H COSY, NOESY, HMBC, HMQC) and relevant literature for 11β-acetoxygedunin (Connolly et al., 1966) and gedunin (Taylor, 1974). ¹H NMR (400 MHz, CDCl₃, δ/p.p.m.): 7.41 (d, 1H, J= 1.3 Hz, 21-H), 7.41 (d, 1H, J = 1.3 Hz, 23-H), 7.07 (d, 1H, J = 10.1 Hz, 1-H), 6.33 (t, 1H, J = 1.3 Hz, 22-H), 5.94 (d, 1H, J = 10.1 Hz, 2-H), 5.61 (s, 1H, 17-H), 5.27 (dd, 1H, J = 12.4 and 2.4 Hz, 6-H), 4.89 (d, 1H, J = 2.4 Hz, 7-H), 3.61 (s, 1H, 15-H), 2.53 (m, 1H, 9-H), 2.52 (d, 1H, J = 12.4 Hz, 5-H), 2.15 (s, 3H, 7-OAc), 2.03 (s, 3H, 6-OAc), 1.60, 1.35, 1.30, and 1.10 (m, 1H each, 11-H2 and 12-H2), 1.27 (s, 3H, 26-H3), 1.26 (s, 3H, 24-H3), 1.24 (s, 3H, 18-H3), 1.21 (s, 3H, 19-H3), 1.17 (s, 3H, 25-H3). ¹³C NMR (CDCl₃, δ/p.p.m.): 204.1 (s, C-3), 170.1 and 170.0 (s, 6- and 7-acetyl CO), 167.1 (s, C-16), 156.2 (d, C-1), 143.1 (d, C-23), 141.2 (d, C-21), 126.6 (d, C-2), 120.3 (s, C-20), 109.8 (d, C-22), 78.1 (d, C-17), 72.6 (d, C-7), 69.7 (d, C-6), 69.5 (s, C-14), 56.2 (d, C-15), 47.8 (d, C-5), 44.9 (s, C-4), 43.1 (s, C-8), 40.6 (s, C10), 48.8 (s, C-13), 38.4 (d, C-9), 31.6 (q, C-24), 25.9 (t, C-12), 21.4 (q, C-19), 21.2 (q, 6-acetyl CH₃), 20.9 (q, 7-acetyl CH₃), 20.2 (q, C-25), 18.1 (q, C-26), 17.9 (q, C-18), 15.0 (t, C-11).

Computing details top

Data collection: SMART (Bruker, 2003); cell refinement: SAINT (Bruker, 2003); data reduction: SAINT, SADABS and XPREP (Bruker, 2003); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

	Fig. 1. The structure of the title compound, showing 50% probability displacement ellipsoids and the atom-numbering scheme.
	Fig. 2. Superposition plot of the title compound (red) and 11α-hydroxygedunin (Mitsui et al., 2006; two independent molecules in blue and pink) after least squares fit of the A/B/C/D rings.
	Fig. 3. Superposition plot of the title compound (red) and gedunin (Toscano et al., 1996; green) after least squares fit of the B/C/D rings. The distance between the two terminal keto oxygen atoms O(1) (leftmost red and green atom) is 2.01 Å.
	Fig. 4. Superposition plot the title compound (red) and 7-oxogedunin (Waratchareeyakul et al., 2004; cyan) after least squares fit of the A/B/C/D rings. Note the difference in torsion angle T2 = C9—C11—C12—C13 (upper part of ring C), which is +14.2 (2)° in 6α-acetoxygedunin and -38.9° in 7-oxogedunin.
	Fig. 5. Packing diagram of 6α-acetoxygedunin viewed down the a axis.

(1S,3aS,4aR,4bS,5S,6R, 6aR,10aR,10bR,12aS)-5,6-bis(acetyloxy)- 1-(3-furyl)-1,5,6,6a,7,10a,10b,11,12,12a-decahydro-4b,7,7,10a,12a- pentamethyloxireno[c]phenanthro[1,2-d]pyran- 3,8(3aH,4bH)-dione top

Crystal data top

C₃₀H₃₆O₉	F(000) = 1152
M_r = 540.59	D_x = 1.295 Mg m⁻³
Orthorhombic, P2₁2₁2₁	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ac 2ab	Cell parameters from 852 reflections
a = 6.475 (2) Å	θ = 2.4–29.8°
b = 14.914 (5) Å	µ = 0.10 mm⁻¹
c = 28.713 (9) Å	T = 173 K
V = 2772.8 (15) Å³	Prism, colourless
Z = 4	0.62 × 0.40 × 0.25 mm

Data collection top

Bruker SMART APEX CCD diffractometer	4509 independent reflections
Radiation source: fine-focus sealed tube	4077 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.031
ω scans	θ_max = 30.0°, θ_min = 2.5°
Absorption correction: multi-scan (SADABS; Bruker, 2003)	h = −9→9
T_min = 0.89, T_max = 0.98	k = −20→20
39048 measured reflections	l = −40→40

Refinement top

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)] = 0.037	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.099	H-atom parameters constrained
S = 1.04	w = 1/[σ²(F_o²) + (0.0617P)² + 0.3403P] where P = (F_o² + 2F_c²)/3
4509 reflections	(Δ/σ)_max < 0.001
359 parameters	Δρ_max = 0.26 e Å⁻³
0 restraints	Δρ_min = −0.24 e Å⁻³

Crystal data top

C₃₀H₃₆O₉	V = 2772.8 (15) Å³
M_r = 540.59	Z = 4
Orthorhombic, P2₁2₁2₁	Mo Kα radiation
a = 6.475 (2) Å	µ = 0.10 mm⁻¹
b = 14.914 (5) Å	T = 173 K
c = 28.713 (9) Å	0.62 × 0.40 × 0.25 mm

Data collection top

Bruker SMART APEX CCD diffractometer	4509 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2003)	4077 reflections with I > 2σ(I)
T_min = 0.89, T_max = 0.98	R_int = 0.031
39048 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.037	0 restraints
wR(F²) = 0.099	H-atom parameters constrained
S = 1.04	Δρ_max = 0.26 e Å⁻³
4509 reflections	Δρ_min = −0.24 e Å⁻³
359 parameters

Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
O1	0.0587 (3)	0.73999 (11)	0.23019 (6)	0.0535 (4)
O2	0.3222 (2)	0.68452 (7)	0.40284 (4)	0.0308 (3)
O3	0.21379 (17)	0.50631 (7)	0.42004 (3)	0.0218 (2)
O4	0.67376 (18)	0.33557 (9)	0.41784 (4)	0.0303 (3)
O5	0.3916 (2)	0.20217 (8)	0.45502 (4)	0.0311 (3)
O6	0.3600 (2)	0.29114 (9)	0.51630 (4)	0.0371 (3)
O7	0.3049 (7)	−0.02998 (11)	0.35841 (9)	0.1021 (11)
O8	0.6555 (3)	0.70255 (12)	0.42549 (6)	0.0546 (4)
O9	0.3152 (3)	0.55979 (10)	0.49051 (4)	0.0413 (3)
C1	0.1155 (3)	0.51480 (13)	0.26444 (5)	0.0295 (3)
H1	0.0712	0.4558	0.2569	0.035*
C2	0.0178 (3)	0.58569 (14)	0.24571 (6)	0.0342 (4)
H2	−0.0937	0.5765	0.2247	0.041*
C3	0.0830 (3)	0.67781 (14)	0.25763 (6)	0.0354 (4)
C4	0.1727 (3)	0.69563 (11)	0.30666 (6)	0.0289 (3)
C5	0.2297 (2)	0.60496 (10)	0.33182 (5)	0.0220 (3)
H5	0.0998	0.5837	0.3471	0.026*
C6	0.3893 (2)	0.61484 (10)	0.37098 (5)	0.0230 (3)
H6	0.5258	0.6318	0.3573	0.028*
C7	0.4135 (2)	0.52809 (10)	0.39934 (5)	0.0210 (3)
H7	0.5176	0.5376	0.4246	0.025*
C8	0.4803 (2)	0.44830 (10)	0.36887 (5)	0.0198 (3)
C9	0.3279 (2)	0.43982 (10)	0.32698 (5)	0.0208 (3)
H9	0.1901	0.4274	0.3413	0.025*
C10	0.2973 (2)	0.52800 (10)	0.29783 (5)	0.0217 (3)
C11	0.3781 (3)	0.35593 (11)	0.29761 (5)	0.0302 (3)
H11A	0.4995	0.3692	0.2778	0.036*
H11B	0.2600	0.3436	0.2767	0.036*
C12	0.4241 (3)	0.27008 (11)	0.32647 (6)	0.0300 (3)
H12A	0.3503	0.2188	0.3122	0.036*
H12B	0.5739	0.2572	0.3249	0.036*
C13	0.3597 (2)	0.27762 (10)	0.37810 (5)	0.0230 (3)
C14	0.4749 (2)	0.35925 (10)	0.39801 (5)	0.0210 (3)
C15	0.5091 (2)	0.35775 (11)	0.44934 (5)	0.0248 (3)
H15	0.5181	0.4171	0.4654	0.030*
C16	0.4171 (3)	0.28141 (11)	0.47670 (5)	0.0268 (3)
C17	0.4394 (3)	0.19354 (11)	0.40509 (6)	0.0325 (4)
H17	0.5926	0.1892	0.4012	0.039*
C18	0.1228 (2)	0.28506 (11)	0.38491 (5)	0.0254 (3)
H18A	0.0824	0.3484	0.3851	0.038*
H18B	0.0840	0.2574	0.4146	0.038*
H18C	0.0522	0.2541	0.3594	0.038*
C19	0.4839 (3)	0.55432 (12)	0.26637 (5)	0.0286 (3)
H19A	0.5308	0.5016	0.2490	0.043*
H19B	0.5969	0.5767	0.2859	0.043*
H19C	0.4413	0.6012	0.2445	0.043*
C20	0.3434 (4)	0.10558 (12)	0.39106 (7)	0.0455 (5)
C21	0.4335 (7)	0.04307 (15)	0.36416 (10)	0.0767 (11)
H21	0.5673	0.0484	0.3509	0.092*
C22	0.1459 (5)	0.06906 (14)	0.40432 (10)	0.0588 (7)
H22	0.0451	0.0969	0.4235	0.071*
C23	0.1322 (8)	−0.01205 (18)	0.38421 (13)	0.0876 (13)
H23	0.0181	−0.0516	0.3875	0.105*
C24	−0.0104 (3)	0.74131 (13)	0.33278 (7)	0.0399 (4)
H24A	−0.0409	0.7993	0.3182	0.060*
H24B	0.0274	0.7507	0.3655	0.060*
H24C	−0.1327	0.7027	0.3311	0.060*
C25	0.3518 (3)	0.76299 (12)	0.30263 (7)	0.0367 (4)
H25A	0.3057	0.8158	0.2852	0.055*
H25B	0.4678	0.7348	0.2863	0.055*
H25C	0.3961	0.7813	0.3339	0.055*
C26	0.7086 (2)	0.46280 (12)	0.35367 (6)	0.0269 (3)
H26A	0.7211	0.5204	0.3375	0.040*
H26B	0.7507	0.4142	0.3327	0.040*
H26C	0.7978	0.4629	0.3813	0.040*
C27	0.4760 (4)	0.72270 (14)	0.42919 (7)	0.0419 (5)
C28	0.3892 (6)	0.79118 (17)	0.46226 (9)	0.0655 (8)
H28A	0.4966	0.8349	0.4702	0.098*
H28B	0.3415	0.7612	0.4907	0.098*
H28C	0.2729	0.8221	0.4475	0.098*
C29	0.1864 (3)	0.52448 (11)	0.46639 (5)	0.0268 (3)
C30	−0.0241 (3)	0.49403 (14)	0.48189 (6)	0.0382 (4)
H30A	−0.0316	0.4956	0.5160	0.057*
H30B	−0.0485	0.4327	0.4710	0.057*
H30C	−0.1294	0.5340	0.4688	0.057*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.0596 (10)	0.0553 (9)	0.0454 (8)	0.0088 (8)	−0.0091 (7)	0.0263 (7)
O2	0.0402 (7)	0.0240 (5)	0.0281 (5)	−0.0007 (5)	0.0018 (5)	−0.0018 (4)
O3	0.0219 (5)	0.0257 (5)	0.0177 (4)	−0.0016 (4)	0.0032 (4)	0.0006 (4)
O4	0.0194 (5)	0.0432 (6)	0.0284 (5)	0.0036 (5)	0.0000 (4)	0.0133 (5)
O5	0.0357 (6)	0.0287 (6)	0.0289 (6)	−0.0005 (5)	−0.0027 (5)	0.0088 (5)
O6	0.0407 (7)	0.0463 (7)	0.0242 (5)	−0.0066 (6)	0.0035 (5)	0.0092 (5)
O7	0.200 (3)	0.0281 (8)	0.0781 (14)	0.0038 (15)	−0.016 (2)	−0.0129 (8)
O8	0.0467 (9)	0.0676 (10)	0.0496 (8)	−0.0210 (8)	−0.0039 (7)	−0.0149 (8)
O9	0.0463 (8)	0.0528 (8)	0.0247 (5)	−0.0105 (7)	0.0018 (6)	−0.0083 (6)
C1	0.0263 (8)	0.0408 (9)	0.0213 (6)	−0.0019 (7)	−0.0024 (6)	0.0031 (6)
C2	0.0247 (8)	0.0528 (10)	0.0251 (7)	0.0013 (8)	−0.0037 (6)	0.0097 (7)
C3	0.0259 (8)	0.0483 (10)	0.0319 (8)	0.0067 (8)	0.0012 (7)	0.0147 (7)
C4	0.0283 (8)	0.0298 (7)	0.0285 (7)	0.0048 (7)	0.0039 (6)	0.0101 (6)
C5	0.0198 (6)	0.0259 (7)	0.0202 (6)	0.0005 (5)	0.0021 (5)	0.0052 (5)
C6	0.0242 (7)	0.0232 (7)	0.0215 (6)	−0.0016 (6)	0.0023 (6)	0.0006 (5)
C7	0.0198 (6)	0.0250 (7)	0.0182 (6)	−0.0022 (5)	0.0004 (5)	0.0015 (5)
C8	0.0178 (6)	0.0238 (6)	0.0179 (6)	0.0006 (5)	0.0002 (5)	0.0035 (5)
C9	0.0211 (6)	0.0248 (6)	0.0166 (6)	−0.0007 (6)	0.0007 (5)	0.0023 (5)
C10	0.0205 (6)	0.0278 (7)	0.0169 (6)	0.0005 (6)	0.0011 (5)	0.0037 (5)
C11	0.0451 (10)	0.0276 (7)	0.0178 (6)	0.0009 (7)	0.0028 (7)	−0.0010 (6)
C12	0.0372 (9)	0.0284 (7)	0.0244 (7)	0.0084 (7)	0.0042 (6)	−0.0021 (6)
C13	0.0253 (7)	0.0213 (6)	0.0224 (6)	0.0049 (6)	0.0016 (5)	0.0015 (5)
C14	0.0184 (6)	0.0259 (7)	0.0187 (6)	0.0027 (5)	0.0010 (5)	0.0037 (5)
C15	0.0224 (7)	0.0308 (7)	0.0212 (6)	−0.0018 (6)	−0.0020 (6)	0.0065 (5)
C16	0.0229 (7)	0.0325 (8)	0.0249 (7)	−0.0006 (6)	−0.0026 (6)	0.0093 (6)
C17	0.0406 (9)	0.0257 (7)	0.0311 (8)	0.0103 (7)	0.0012 (7)	0.0049 (6)
C18	0.0242 (7)	0.0258 (7)	0.0262 (7)	−0.0016 (6)	−0.0013 (6)	0.0031 (6)
C19	0.0257 (7)	0.0383 (8)	0.0217 (6)	0.0022 (7)	0.0056 (6)	0.0082 (6)
C20	0.0767 (16)	0.0233 (8)	0.0365 (9)	0.0091 (10)	−0.0058 (10)	0.0034 (7)
C21	0.138 (3)	0.0313 (10)	0.0610 (15)	0.0238 (15)	0.0115 (19)	−0.0033 (10)
C22	0.0819 (18)	0.0284 (9)	0.0661 (14)	−0.0109 (11)	−0.0189 (14)	0.0047 (9)
C23	0.142 (4)	0.0335 (12)	0.087 (2)	−0.0168 (18)	−0.032 (3)	−0.0012 (13)
C24	0.0366 (9)	0.0372 (9)	0.0458 (10)	0.0111 (8)	0.0102 (8)	0.0104 (8)
C25	0.0387 (9)	0.0318 (8)	0.0397 (9)	−0.0024 (7)	0.0049 (8)	0.0140 (7)
C26	0.0180 (6)	0.0364 (8)	0.0263 (7)	0.0001 (6)	0.0030 (6)	0.0083 (6)
C27	0.0607 (13)	0.0341 (9)	0.0309 (8)	−0.0134 (9)	−0.0003 (9)	−0.0065 (7)
C28	0.095 (2)	0.0476 (13)	0.0538 (13)	−0.0037 (15)	−0.0014 (14)	−0.0251 (11)
C29	0.0343 (8)	0.0266 (7)	0.0195 (6)	−0.0010 (7)	0.0055 (6)	−0.0014 (5)
C30	0.0412 (10)	0.0434 (10)	0.0299 (8)	−0.0086 (8)	0.0164 (7)	−0.0055 (7)

Geometric parameters (Å, º) top

O1—C3	1.227 (2)	C12—C13	1.544 (2)
O2—C27	1.374 (3)	C12—H12A	0.9900
O2—C6	1.4510 (18)	C12—H12B	0.9900
O3—C29	1.3697 (18)	C13—C14	1.538 (2)
O3—C7	1.4600 (18)	C13—C18	1.551 (2)
O4—C15	1.436 (2)	C13—C17	1.562 (2)
O4—C14	1.4517 (18)	C14—C15	1.491 (2)
O5—C16	1.346 (2)	C15—C16	1.506 (2)
O5—C17	1.472 (2)	C15—H15	1.0000
O6—C16	1.204 (2)	C17—C20	1.507 (3)
O7—C23	1.368 (6)	C17—H17	1.0000
O7—C21	1.381 (5)	C18—H18A	0.9800
O8—C27	1.205 (3)	C18—H18B	0.9800
O9—C29	1.205 (2)	C18—H18C	0.9800
C1—C2	1.344 (2)	C19—H19A	0.9800
C1—C10	1.531 (2)	C19—H19B	0.9800
C1—H1	0.9500	C19—H19C	0.9800
C2—C3	1.478 (3)	C20—C21	1.344 (3)
C2—H2	0.9500	C20—C22	1.441 (4)
C3—C4	1.546 (3)	C21—H21	0.9500
C4—C25	1.539 (3)	C22—C23	1.343 (4)
C4—C24	1.560 (3)	C22—H22	0.9500
C4—C5	1.577 (2)	C23—H23	0.9500
C5—C6	1.534 (2)	C24—H24A	0.9800
C5—C10	1.569 (2)	C24—H24B	0.9800
C5—H5	1.0000	C24—H24C	0.9800
C6—C7	1.537 (2)	C25—H25A	0.9800
C6—H6	1.0000	C25—H25B	0.9800
C7—C8	1.539 (2)	C25—H25C	0.9800
C7—H7	1.0000	C26—H26A	0.9800
C8—C26	1.557 (2)	C26—H26B	0.9800
C8—C9	1.561 (2)	C26—H26C	0.9800
C8—C14	1.570 (2)	C27—C28	1.504 (3)
C9—C11	1.544 (2)	C28—H28A	0.9800
C9—C10	1.571 (2)	C28—H28B	0.9800
C9—H9	1.0000	C28—H28C	0.9800
C10—C19	1.559 (2)	C29—C30	1.504 (3)
C11—C12	1.554 (2)	C30—H30A	0.9800
C11—H11A	0.9900	C30—H30B	0.9800
C11—H11B	0.9900	C30—H30C	0.9800

C27—O2—C6	115.28 (15)	C15—C14—C8	122.44 (13)
C29—O3—C7	117.80 (12)	C13—C14—C8	118.83 (12)
C15—O4—C14	62.14 (9)	O4—C15—C14	59.43 (9)
C16—O5—C17	120.09 (12)	O4—C15—C16	116.61 (14)
C23—O7—C21	105.9 (2)	C14—C15—C16	117.91 (14)
C2—C1—C10	120.74 (16)	O4—C15—H15	116.8
C2—C1—H1	119.6	C14—C15—H15	116.8
C10—C1—H1	119.6	C16—C15—H15	116.8
C1—C2—C3	120.26 (16)	O6—C16—O5	120.32 (15)
C1—C2—H2	119.9	O6—C16—C15	121.52 (16)
C3—C2—H2	119.9	O5—C16—C15	118.11 (14)
O1—C3—C2	121.14 (18)	O5—C17—C20	104.45 (14)
O1—C3—C4	120.21 (19)	O5—C17—C13	110.09 (13)
C2—C3—C4	118.58 (14)	C20—C17—C13	115.47 (15)
C25—C4—C3	109.08 (14)	O5—C17—H17	108.9
C25—C4—C24	108.90 (16)	C20—C17—H17	108.9
C3—C4—C24	103.16 (15)	C13—C17—H17	108.9
C25—C4—C5	114.70 (14)	C13—C18—H18A	109.5
C3—C4—C5	110.96 (14)	C13—C18—H18B	109.5
C24—C4—C5	109.39 (13)	H18A—C18—H18B	109.5
C6—C5—C10	109.77 (12)	C13—C18—H18C	109.5
C6—C5—C4	114.27 (13)	H18A—C18—H18C	109.5
C10—C5—C4	114.05 (12)	H18B—C18—H18C	109.5
C6—C5—H5	106.0	C10—C19—H19A	109.5
C10—C5—H5	106.0	C10—C19—H19B	109.5
C4—C5—H5	106.0	H19A—C19—H19B	109.5
O2—C6—C5	109.22 (12)	C10—C19—H19C	109.5
O2—C6—C7	107.43 (12)	H19A—C19—H19C	109.5
C5—C6—C7	112.10 (12)	H19B—C19—H19C	109.5
O2—C6—H6	109.3	C21—C20—C22	106.0 (3)
C5—C6—H6	109.3	C21—C20—C17	125.3 (3)
C7—C6—H6	109.3	C22—C20—C17	128.7 (2)
O3—C7—C6	108.21 (12)	C20—C21—O7	110.8 (4)
O3—C7—C8	107.95 (11)	C20—C21—H21	124.6
C6—C7—C8	112.24 (12)	O7—C21—H21	124.6
O3—C7—H7	109.5	C23—C22—C20	106.6 (3)
C6—C7—H7	109.5	C23—C22—H22	126.7
C8—C7—H7	109.5	C20—C22—H22	126.7
C7—C8—C26	108.58 (13)	C22—C23—O7	110.8 (4)
C7—C8—C9	108.85 (12)	C22—C23—H23	124.6
C26—C8—C9	113.32 (11)	O7—C23—H23	124.6
C7—C8—C14	110.18 (11)	C4—C24—H24A	109.5
C26—C8—C14	106.74 (12)	C4—C24—H24B	109.5
C9—C8—C14	109.15 (12)	H24A—C24—H24B	109.5
C11—C9—C8	110.69 (12)	C4—C24—H24C	109.5
C11—C9—C10	114.45 (11)	H24A—C24—H24C	109.5
C8—C9—C10	114.98 (12)	H24B—C24—H24C	109.5
C11—C9—H9	105.2	C4—C25—H25A	109.5
C8—C9—H9	105.2	C4—C25—H25B	109.5
C10—C9—H9	105.2	H25A—C25—H25B	109.5
C1—C10—C19	105.40 (12)	C4—C25—H25C	109.5
C1—C10—C5	105.61 (13)	H25A—C25—H25C	109.5
C19—C10—C5	113.12 (13)	H25B—C25—H25C	109.5
C1—C10—C9	108.83 (13)	C8—C26—H26A	109.5
C19—C10—C9	114.95 (13)	C8—C26—H26B	109.5
C5—C10—C9	108.42 (11)	H26A—C26—H26B	109.5
C9—C11—C12	114.64 (12)	C8—C26—H26C	109.5
C9—C11—H11A	108.6	H26A—C26—H26C	109.5
C12—C11—H11A	108.6	H26B—C26—H26C	109.5
C9—C11—H11B	108.6	O8—C27—O2	123.16 (18)
C12—C11—H11B	108.6	O8—C27—C28	125.8 (2)
H11A—C11—H11B	107.6	O2—C27—C28	111.0 (2)
C13—C12—C11	113.60 (13)	C27—C28—H28A	109.5
C13—C12—H12A	108.8	C27—C28—H28B	109.5
C11—C12—H12A	108.8	H28A—C28—H28B	109.5
C13—C12—H12B	108.8	C27—C28—H28C	109.5
C11—C12—H12B	108.8	H28A—C28—H28C	109.5
H12A—C12—H12B	107.7	H28B—C28—H28C	109.5
C14—C13—C12	106.49 (13)	O9—C29—O3	123.71 (16)
C14—C13—C18	112.10 (13)	O9—C29—C30	126.10 (15)
C12—C13—C18	113.16 (13)	O3—C29—C30	110.19 (14)
C14—C13—C17	106.91 (13)	C29—C30—H30A	109.5
C12—C13—C17	109.19 (13)	C29—C30—H30B	109.5
C18—C13—C17	108.77 (14)	H30A—C30—H30B	109.5
O4—C14—C15	58.43 (9)	C29—C30—H30C	109.5
O4—C14—C13	112.54 (12)	H30A—C30—H30C	109.5
C15—C14—C13	115.33 (12)	H30B—C30—H30C	109.5
O4—C14—C8	113.27 (12)

C10—C1—C2—C3	−0.8 (3)	C11—C12—C13—C18	66.3 (2)
C1—C2—C3—O1	151.7 (2)	C11—C12—C13—C17	−172.40 (15)
C1—C2—C3—C4	−31.5 (3)	C15—O4—C14—C13	−106.78 (14)
O1—C3—C4—C25	−41.8 (2)	C15—O4—C14—C8	114.90 (14)
C2—C3—C4—C25	141.42 (17)	C12—C13—C14—O4	−90.70 (14)
O1—C3—C4—C24	73.9 (2)	C18—C13—C14—O4	145.05 (12)
C2—C3—C4—C24	−102.93 (18)	C17—C13—C14—O4	25.94 (16)
O1—C3—C4—C5	−169.06 (17)	C12—C13—C14—C15	−155.18 (13)
C2—C3—C4—C5	14.1 (2)	C18—C13—C14—C15	80.56 (16)
C25—C4—C5—C6	33.94 (19)	C17—C13—C14—C15	−38.54 (18)
C3—C4—C5—C6	158.10 (13)	C12—C13—C14—C8	45.10 (17)
C24—C4—C5—C6	−88.73 (17)	C18—C13—C14—C8	−79.16 (16)
C25—C4—C5—C10	−93.47 (17)	C17—C13—C14—C8	161.74 (13)
C3—C4—C5—C10	30.69 (18)	C7—C8—C14—O4	−95.19 (14)
C24—C4—C5—C10	143.86 (15)	C26—C8—C14—O4	22.52 (16)
C27—O2—C6—C5	−157.85 (14)	C9—C8—C14—O4	145.34 (12)
C27—O2—C6—C7	80.34 (16)	C7—C8—C14—C15	−28.89 (19)
C10—C5—C6—O2	−178.48 (11)	C26—C8—C14—C15	88.82 (16)
C4—C5—C6—O2	51.94 (16)	C9—C8—C14—C15	−148.36 (14)
C10—C5—C6—C7	−59.54 (15)	C7—C8—C14—C13	129.32 (13)
C4—C5—C6—C7	170.89 (12)	C26—C8—C14—C13	−112.97 (14)
C29—O3—C7—C6	−103.01 (14)	C9—C8—C14—C13	9.85 (17)
C29—O3—C7—C8	135.29 (13)	C14—O4—C15—C16	108.19 (15)
O2—C6—C7—O3	59.79 (15)	C13—C14—C15—O4	101.94 (14)
C5—C6—C7—O3	−60.21 (15)	C8—C14—C15—O4	−99.15 (15)
O2—C6—C7—C8	178.81 (12)	O4—C14—C15—C16	−106.01 (16)
C5—C6—C7—C8	58.81 (16)	C13—C14—C15—C16	−4.1 (2)
O3—C7—C8—C26	−170.06 (11)	C8—C14—C15—C16	154.85 (14)
C6—C7—C8—C26	70.76 (15)	C17—O5—C16—O6	172.96 (16)
O3—C7—C8—C9	66.16 (14)	C17—O5—C16—C15	−4.3 (2)
C6—C7—C8—C9	−53.01 (16)	O4—C15—C16—O6	143.88 (16)
O3—C7—C8—C14	−53.49 (14)	C14—C15—C16—O6	−148.35 (16)
C6—C7—C8—C14	−172.67 (12)	O4—C15—C16—O5	−38.9 (2)
C7—C8—C9—C11	−175.38 (12)	C14—C15—C16—O5	28.8 (2)
C26—C8—C9—C11	63.71 (16)	C16—O5—C17—C20	−166.21 (16)
C14—C8—C9—C11	−55.09 (15)	C16—O5—C17—C13	−41.7 (2)
C7—C8—C9—C10	53.01 (15)	C14—C13—C17—O5	61.47 (17)
C26—C8—C9—C10	−67.90 (16)	C12—C13—C17—O5	176.30 (14)
C14—C8—C9—C10	173.30 (12)	C18—C13—C17—O5	−59.77 (18)
C2—C1—C10—C19	−75.97 (19)	C14—C13—C17—C20	179.41 (16)
C2—C1—C10—C5	44.02 (19)	C12—C13—C17—C20	−65.8 (2)
C2—C1—C10—C9	160.24 (15)	C18—C13—C17—C20	58.2 (2)
C6—C5—C10—C1	172.32 (12)	O5—C17—C20—C21	−135.9 (2)
C4—C5—C10—C1	−57.99 (16)	C13—C17—C20—C21	103.1 (3)
C6—C5—C10—C19	−72.91 (15)	O5—C17—C20—C22	41.4 (3)
C4—C5—C10—C19	56.78 (17)	C13—C17—C20—C22	−79.6 (2)
C6—C5—C10—C9	55.81 (15)	C22—C20—C21—O7	1.5 (3)
C4—C5—C10—C9	−174.49 (12)	C17—C20—C21—O7	179.3 (2)
C11—C9—C10—C1	61.00 (17)	C23—O7—C21—C20	−2.0 (3)
C8—C9—C10—C1	−169.21 (12)	C21—C20—C22—C23	−0.3 (3)
C11—C9—C10—C19	−56.92 (18)	C17—C20—C22—C23	−178.1 (2)
C8—C9—C10—C19	72.88 (16)	C20—C22—C23—O7	−0.9 (3)
C11—C9—C10—C5	175.40 (13)	C21—O7—C23—C22	1.8 (4)
C8—C9—C10—C5	−54.81 (16)	C6—O2—C27—O8	2.3 (3)
C8—C9—C11—C12	43.91 (19)	C6—O2—C27—C28	−177.72 (17)
C10—C9—C11—C12	175.79 (14)	C7—O3—C29—O9	2.3 (2)
C9—C11—C12—C13	14.2 (2)	C7—O3—C29—C30	−177.55 (13)
C11—C12—C13—C14	−57.29 (18)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C11—H11B···O1ⁱ	0.99	2.59	3.410 (3)	141
C18—H18C···O1ⁱ	0.98	2.68	3.571 (2)	152
C18—H18B···O6ⁱⁱ	0.98	2.56	3.497 (2)	160
C22—H22···O6ⁱⁱ	0.95	2.69	3.601 (3)	162
C24—H24B···O2	0.98	2.40	3.066 (3)	125
C25—H25C···O2	0.98	2.50	3.112 (2)	121
C5—H5···O3	1.00	2.50	2.931 (2)	105
C9—H9···O3	1.00	2.55	2.944 (2)	103
C18—H18B···O5	0.98	2.45	2.934 (2)	110
C7—H7···O9	1.00	2.33	2.735 (2)	103

Symmetry codes: (i) −x, y−1/2, −z+1/2; (ii) x−1/2, −y+1/2, −z+1.

Experimental details

Crystal data
Chemical formula	C₃₀H₃₆O₉
M_r	540.59
Crystal system, space group	Orthorhombic, P2₁2₁2₁
Temperature (K)	173
a, b, c (Å)	6.475 (2), 14.914 (5), 28.713 (9)
V (Å³)	2772.8 (15)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.10
Crystal size (mm)	0.62 × 0.40 × 0.25

Data collection
Diffractometer	Bruker SMART APEX CCD diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2003)
T_min, T_max	0.89, 0.98
No. of measured, independent and observed [I > 2σ(I)] reflections	39048, 4509, 4077
R_int	0.031
(sin θ/λ)_max (Å⁻¹)	0.703

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.037, 0.099, 1.04
No. of reflections	4509
No. of parameters	359
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.26, −0.24

Computer programs: SMART (Bruker, 2003), SAINT (Bruker, 2003), SAINT, SADABS and XPREP (Bruker, 2003), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).