Isolation of a Bis-Iodurated Tetra-THF as a Trace Product from the Oxidation of Squalene with RuO4 and Its Double Ring Expansion to a Novel bis-THF-bis-THP Compound

A novel bis-iodurated polyether compound, based on an unprecedented tetra-THF backbone, has been isolated as a trace by-product of the oxidation of squalene with the catalytic system RuO2(cat.)/NaIO4. The double erythro configuration of the central portion of the molecule furnishes the first indirect support of the previously postulated pathway operating in the oxidative pentacyclization of the isoprenoid substrate. A bidirectional double oxidative bis-cyclization is invoked to explain the formation of this compound. The isolated substance was successfully subjected to a double rearrangement-ring expansion to give a novel bis-THF-bis-THP compound.


Introduction
Some years ago we discovered a novel cascade process catalysed by RuO 4 generated in situ by the action of NaIO 4 on RuO 2 , the pre-catalytic species employed to generate RuO 4 [1]. This is a unique process by which a poly-THF backbone, made up of adjacently linked THF rings, can be built-up in a single step and in a stereoselective manner starting from polyenes characterized by a repetitive 1,5-diene structural motif [2][3][4][5][6][7][8]. In particular, oxidation of squalene gives rise to penta-THF compound 1 (Scheme 1) containing ten stereogenic centres. Previous studies carried out in our group had suggested that steric and chelation control factors concur to determine the stereochemical outcome of the process [6].  .

Oxidative pentacyclization
In a more recent investigation, the use of different cyclization conditions led to a different stereochemistry of the process [9]. In particular, four new C 30 isomeric heptacyclic polyether substances (compounds 2-5, Scheme 2) were obtained through a unique seven-step cascade process featuring a pentacyclization of squalene followed by a double oxidative spiroketalization at the two bis-THF termini of the first-formed penta-THF intermediates. Careful HPLC isolation of latter substances for X-ray studies [9] allowed also the isolation of tetra-THF 6 (Scheme 2), a very minor side-product of the process, possessing a C S -symmetric structure embodying two terminal cis-threotrans bis-THF moieties connected by a central bis-iodurated tetracarbonious segment. The determination of the stereostructure of compound 6, the mechanistic implication of its isolation as well as its double rearrangement-ring expansion to a new bis-THP polyether compound, are discussed in the present paper. Four isomers

Chemistry
The structure of compound 6 was determined by X-ray diffraction analysis carried out on a single crystal of the substance obtained by slow evaporation of a chloroform solution. The most interesting, and unusual feature of this compound is the double erythro configuration around the C10/C11 and C14/C15 bonds. In fact, previous studies from our group had demonstrated that the oxidation of both linear and isoprenoid polyenes constantly furnishes poly-THF compounds possessing threo inter-THF relationships. This is consistent with the syn addition (a [3+2] cycloaddition) of a O=Ru-O portion across each involved C-C double bond, along the all-trans polyene chain (Scheme 3), that also agrees with mechanistic proposals for related oxidative mono-cyclization of 1,5-dienes catalysed by RuO 4 [10][11][12][13][14][15] and related oxo-species OsO 4 [16][17][18] and MnO 4 - [19][20][21][22][23][24][25][26][27], as well as rhenium (VII)-mediated oxidative polycyclization of hydroxypolyenes [28][29][30][31]. Based on these precedents, formation of 6 was intriguing and could be rationalised through a double cis/trans-selective oxidative bis-cyclization process (Scheme 4). Each bis-cyclization event involves three consecutive double bonds of the polyene chain starting from the terminal ones. In particular, attack of RuO 4 to the Δ 2 double bond induces two successive cyclization steps giving rise to bis-THF intermediate 8, in the same manner as shown for the synthesis of 1 (see intermediate 7, Scheme 3). A second bis-cyclization would then occur at the other side of the molecule by attack of RuO 4 at the terminal, Δ 22 , double bond to give the all-threo tetra-THF 9 still possessing two oxoruthenate appendages linked to C-11 and C-14. It can be presumed that a double substitution of the rutheniumcontaining portions, with inversion of configuration at involved carbon centres, would then occur during the reductive quenching of the process, by iodide ions probably generated in situ by the action of tiosulphate on iodate in turn produced during the oxidation of RuO 2 to RuO 4 . It cannot be excluded that iodide could originate from reduction of periodate itself not completely consumed in the reaction medium. It is probable that such a side-process could be due to the higher concentration of the reaction medium in the new experimented conditions [9].  In order to enlarge the range of polyether substances accessible through the Ru-mediated polycyclization process we began an exploration of the possible post-synthetic modifications of some of the poly-THF backbones obtained through the above process. We have previously demonstrated that progressive structural simplification of compound 1 to small-sized poly-THF compounds can be achieved via an iterative PCC-mediated oxidative cleavage/reduction [7] sequence. The entire process is possible due to the two alcohol functionalities adjacent to the terminal THF rings that are prone to be intercepted by PCC [32]. In addition, a new type of cytotoxic spyroketal poly-THF compound, strictly related to bis-spiroketals 2-5, could be accessed through a PCC-mediated oxidative spiroketalization process starting from 1 [3]. In a more recent study we have also shown that the same oxidant, or the related system PCC-H 5 IO 6 , is able to attack the angular CH position of the THF ring in various mono and poly-THF substrates leading to either the oxidative opening of the THF ring or the oxidative cleavage of suitable inter-THF bonds [33].
As a continuation of this project, we envisaged that compound 6, possessing a central bis-(α-iodo-THF) portion, could be a good model compound to probe a double rearrangement-ring expansion process involving the two internal THF rings as a means to access a new type of mixed THF-THP polyether compounds further functionalised for successive synthetic manipulations providing access to new polyether polycyclic materials. This type of reaction has previously been carried out on substances containing a single α-iodo-THF subunit [34] but has never been attempted on a substrate containing two α-iodo-THF moieties and, in particular, as far as we know, the double rearrangement-ring expansion of a bis-THF substance has never been accomplished. Related chemistry has been successfully employed for example in the synthesis of salynomicin [25] as well as in the synthesis of a bis-oxepane portion of hemibrevetoxin [35]. Pleasingly, when compound 6 was reacted with excess Ag 2 CO 3 (5 equiv.) in acetone/water (8:2, 40 °C, 4 h), compound 10 was obtained in a 65% yield demonstrating the feasibility of the projected transformation (Scheme 5).
Proof for the structure 10 was gained by chemical and high-field 2D-NMR evidence. Attempted acetylation and benzoylation under standard conditions only delivered unreacted 10 indicating, as expected, the presence of tertiary hydroxyl groups in this compound. In particular, the signals resonating at δ 3.86 and 2.36 were assigned, respectively, to the angular THF proton (H-3) and to the H α -5 proton based on the good agreement of their chemical shift values with those typically exhibited by these protons in strictly analogous poly-THF substances including the same cis-THF-containing substructure, previously synthesised in our laboratories [1][2][3][4][5][6][7][8]. This deduction suggested that the two higher field one-proton resonances at δ 3.26 (H-7) and 3.16 (H-11) could be ascribable to the angular hydrogens in the THP ring.
The good proton dispersion of the signals in the 1 H-NMR spectrum of 10 allowed us to fully analyse some crucial signals. In particular, the presence of a THP ring in 10 was corroborated by J values (J = 12.5, 3.6 Hz) of the H-9 equatorial proton resonating as a clean double triplet at δ 1.89, as expected for an equatorial proton next to a quaternary centre (C-10) in a six-membered ring possessing a chair conformation. In addition, a W coupling observed between the signal at δ 1.54 for H ax -9 and the singlet methyl resonance at δ 1.19, ascribable to the C-10 methyl group, also pointed to the presence of a THP ring and the axial nature of that methyl. W-type long-range couplings were also observed between the singlet resonances at δ 1.23 and 1.05 allowing assignment of these signals to the two methyls belonging to the terminal 2-hydroxyisopropyl group. Similarly, a long-range coupling between the methyl signal at δ 1.12 and the H a -5 resonance at δ 2.36 allowed to assign the former resonance to the angular methyl of the THF ring (C6-Me).
These conclusions were reinforced by data from a very informative 700 MHz NOESY experiment ( Figure 1) that also provided conclusive information on the relative configuration of the C-7, C-10 and C-11 centres belonging to the THP ring in 10. In particular, the cis nature of the THP ring was inferred by the presence of a strong correlation peak between signals for the H-7 and H-11 angular protons. Similarly, the axial nature of the C-10 methyl, was further corroborated by a nOe correlation between its resonance at δ 1.19 and that of the H ax -8 proton at δ 1.74. The rest of nOe cross peaks shown in Figure 1 were in full agreement with the given stereostructure.

X-ray crystallography.
Molecules of 6 in the crystals are centrosymmetric (C i point group) as they lie on crystallographic inversion centres (Figure 2). The molecules have a stretched winding shape, which is due to the double cis-trans sequence of the 2,5-disubstituted THF rings and to the trans-planar conformation of the carbon chain.
The molecular conformation is stabilized by an intramolecular H bonding between O−H donor and the oxygen acceptor of the inner THF ring (O1−H···O3 0.983, 2.224, 3.175(9) Å, 163°). Ring puckering coordinates of the inner THF ring are q 2 = 0.356(6) Å ϕ 2 = 211(1)°, and of the outer are q 2 = 0.316(7) Å ϕ 2 = 324(1)°. On the basis of the calculated phase angles, it can be argued that both are basically in envelope conformation, with C7 and C4 atoms out of the envelope plane. The packing of molecules is accomplished through weak H bonding interactions between iodine atoms as bifurcated acceptors and methyne C−H donors [36]. This is clearly shown in Figure 3

R
. Along a molecules are stacked in layers through van der Waals contacts.

General
All reagents were purchased (Aldrich) at the highest commercial quality and used without further purification. Reactions were monitored by thin-layer chromatography carried out on precoated silica gel plates (Merck 60, F 254 , 0.25 mm thick). Merck silica gel (Kieselgel 40, particle size 0.063-0.200 mm) was used for column chromatography. HPLC separations were carried out on a Varian 2510 apparatus equipped with a Waters R403 dual cell differential refractometer using Phenomenex 250 × 10 mm, Phenomenex 250 × 4.6 mm and Nucleosil 250 × 10 mm columns. NMR experiments were performed on Varian Mercury Plus 400 MHz, Varian Unity Inova 700 MHz and Gemini 200 spectrometers in CDCl 3 . Proton chemical shifts were referenced to the residual CHCl 3 signal (7.26 ppm); 13 C-NMR chemical shifts were referenced to the solvent (77.0 ppm). J values are in Hz. Abbreviations for signal coupling are as follows: s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet. IR spectra were collected on a Jasco FT-IR-430 spectrometer. High Resolution MS spectra were recorded on a Bruker APEX II FT-ICR mass spectrometer using the electrospray ionization (ESI) technique in positive mode.

X-Ray Crystallography
Crystals of 6 suitable for X-ray analysis were obtained from CHCl 3 by slow evaporation of the solvent. Data were collected at 298 K on a Bruker-Nonius Kappa-CCD diffractometer using graphite monochromated MoKα radiation (λ = 0.71073 Å). Data reduction and multi-scan absorption correction were done using SADABS program [37]. The structure was solved by direct methods (SIR97 program [38]) and refined by the full matrix least-squares method on F 2 using SHELXL-97 program [39] with the aid of the program WinGX [40]. Non-hydrogen atoms were refined anisotropically. H atoms of the hydroxy group was located in difference Fourier maps and refined with U iso = 1.2·U eq of the carrier atom. The positions of the other H atoms were determined stereochemically and refined by the riding model with U iso = 1.2·U eq of the carrier atom (1.5·U eq for H atoms of methyl groups). Ring puckering coordinates [41] were determined using the program PARST [42]. The analysis of the crystal packing and the drawing of the molecule were performed using the programs Mercury [43] and ORTEP [44].
Crystal and refinement data are summarized in Table 1. CCDC reference number 821334 contains the supplementary crystallographic data for 6.

Conclusion
In conclusion, the isolation of bis-iodocompound 6 was interesting from both a mechanistic and a synthetic point of view. Its existence among the oxidation products of squalene with RuO 4 was indicative of the existence of an intermediate species (see 9, Scheme 4), carrying oxoruthenium substituents, likely ORuO 3 groups, adjacent to the two internal THF rings, able to undergo a facile nucleophilic displacement, that enforces the mechanistic hypothesis previously put forward to explain the formation of penta-THF 1 from the same substrate (Scheme 3). In addition, the postulated mechanism for the formation of 6 also suggests a new possible use of the RuO 4 -catalysed polycyclization process where suitable polyenes can be induced to undergo bidirectional poly-THFforming oxidative sequences. The facile access to a novel type of bis-THF-bis-THP compound (10) has been demonstrated via a double ring-enlargement process. Studies are in progress to further develop the chemistry presented here toward the synthesis of new THP-containing polyether compounds.