Michael Schelhaas

Bio: Michael Schelhaas is an academic researcher from Monell Chemical Senses Center. The author has contributed to research in topics: Ferrier rearrangement & Total synthesis. The author has an hindex of 3, co-authored 4 publications receiving 271 citations.

Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangement.

Abstract: A highly convergent, stereocontrolled total synthesis of the potent antiproliferative agent (+)-phorboxazole A (1) has been achieved. Highlights of the synthesis include: modified Petasis−Ferrier rearrangements for assembly of both the C(11−15) and C(22−26) cis-tetrahydropyran rings; extension of the Julia olefination to the synthesis of enol ethers; the design, synthesis, and application of a novel bifunctional oxazole linchpin; and Stille coupling of a C(28) trimethyl stannane with a C(29) oxazole triflate. The longest linear sequence leading to (+)-phorboxazole A (1) was 27 steps, with an overall yield of 3%.

Total synthesis of (+)-phorboxazole A.

Abstract: A highly convergent, stereocontrolled total synthesis of the potent antiproliferative agent (+)phorboxazole A (1) has been achieved. Highlights of the synthesis include: modified Petasis-Ferrier rearrangements for assembly of both the C(11-15) and C(22-26) cis-tetrahydropyran rings; extension of the Julia olefination to the synthesis of enol ethers; the design, synthesis, and application of a novel bifunctional oxazole linchpin; and Stille coupling of a C(28) trimethyl stannane with a C(29) oxazole triflate. The longest linear sequence leading to (+)-phorboxazole A (1) was 27 steps, with an overall yield of 3%. Marine sponges comprise a rich source of architecturally complex, biomedically important natural products; examples include the spongistatins, discodermolide, and the tedanolides.1 Despite the structural complexity, the scarcity of these molecules in conjunction with their medicinal importance continues to prompt intense synthetic campaigns. During a recent search for novel marine antifungals, Searle and Molinski2 identified a methanolic extract from the sponge Phorbas sp. which displayed significant activity against Candida albicans. Bioassay-guided extraction, flash chromatography, and subsequent reverse-phase HPLC afforded two isomeric macrolides termed (+)-phorboxazoles A (1) and B (2). The structures of the phorboxazoles, including relative and absolute stereochemistry, were determined via a combination of NMR analyses, degradation studies, and synthetic correlations.3 The bioactivity profile of the phorboxazoles proved exceptional. In addition to the antifungal activity, the phorboxazoles displayed antibiotic activity against saccharomyces carlsberensis. However, it was the antiproliferative activity that elevated the phorboxazoles to the level of premier medicinal targets. Bioassays against the National Cancer Institute panel of 60 human solid tumor cell lines revealed extraordinary activity against the entire panel;2 the mean GI50 value was 1.58 × 10-9 M for both 1 and 2.3a Some cell lines were completely inhibited at the lowest level tested.2 Particularly noteworthy, phorboxazole A (1) inhibited the human colon tumor cell line HCT-116 and the breast cancer cell line MCF7 with GI50 values of 4.36 × 10-10 M and 5.62 × 10-10 M, respectively. These data place the phorboxazoles in the company of the spongistatins,1a collectively the most potent cytostatic agents discovered to date. Although the precise biochemical mode of action remains undefined, (+)-phorboxazole A (1) is known to arrest the cell cycle in S phase but does not inhibit tubulin polymerization or interfere with the integrity of microtubules. Unfortunately, further biological analysis is not possible, because access to the producing sponge is currently restricted.4 Thus, the phorboxazoles will be only available via total synthesis. Not surprisingly, the novel architecture combined with the impressive bioactivity has attracted wide attention in the synthetic community,5 including our own interest.6 In 1998, Forsyth and co-workers4 published the first total synthesis of (+)-phorboxazole A (1); shortly thereafter, Evans and Fitch reported completion of (+)(1) (a) Spongistatin: Pettit, G. R.; Cichacz, Z. A.; Gao, F.; Herald, C. L.; Boyd, M. R.; Schmidt, J. M.; Hooper, J. N. A. J. Org. Chem. 1993, 58, 1302. (b) Discodermolide: Gunasekera, S. P.; Gunasekera, M.; Longley, R. E.; Schulte, G. K. J. Org. Chem. 1990, 55, 4912. Correction: Gunasekera, S. P.; Gunasekera, M.; Longley, R. E.; Schulte, G. K. J. Org. Chem. 1991, 56, 1346. (c) Tedanolide: Schmitz, F. J.; Gunasekera, S. P.; Yalamanchili, G.; Hossain, M. B.; van der Helm, D. J. Am. Chem. Soc. 1984, 106, 7251. (2) Searle, P. A.; Molinski, T. F. J. Am. Chem. Soc. 1995, 117, 8126. (3) (a) Searle, P. A.; Molinski, T. F.; Brzezinski, L. J.; Leahy, J. W. J. Am. Chem. Soc. 1996, 118, 9422. (b) Molinski, T. F. Tetrahedron Lett. 1996, 37, 7879. (4) Forsyth, C. J.; Ahmed, F.; Cink, R. D.; Lee, C. S. J. Am. Chem. Soc. 1998, 120, 5597. (5) (a) Lee, C. S.; Forsyth, C. J. Tetrahedron Lett. 1996, 37, 6449. (b) Cink, R. D.; Forsyth, C. J. J. Org. Chem. 1997, 62, 5672. (c) Ahmed, F.; Forsyth, C. J. Tetrahedron Lett. 1998, 39, 183. (d) Ye, T.; Pattenden, G. Tetrahedron Lett. 1998, 39, 319. (e) Pattenden, G.; Plowright, A. T.; Tornos, J. A.; Ye, T. Tetrahedron Lett. 1998, 39, 6099. (f) Paterson, I.; Arnott, E. A. Tetrahedron Lett. 1998, 39, 7185. (g) Wolbers, P.; Hoffmann, H. M. R. Tetrahedron 1999, 55, 1905. (h) Misske, A. M.; Hoffmann, H. M. R. Tetrahedron 1999, 55, 4315. (i) Williams, D. R.; Clark, M. P.; Berliner, M. A. Tetrahedron Lett. 1999, 40, 2287. (j) Williams, D. R.; Clark, M. P. Tetrahedron Lett. 1999, 40, 2291. (k) Wolbers, P.; Hoffmann, H. M. R. Synthesis 1999, 797. (l) Evans, D. A.; Cee, V. J.; Smith, T. E.; Santiago, K. J. Org. Lett. 1999, 1, 87. (m) Wolbers, P.; Misske, A. M.; Hoffmann, H. M. R. Tetrahedron Lett. 1999, 40, 4527. (n) Wolbers, P.; Hoffmann, H. M. R.; Sasse, F. Synlett 1999, 11, 1808. (o) Pattenden, G.; Plowright, A. T. Tetrahedron Lett. 2000, 41, 983. (p) Schaus, J. V.; Panek, J. S. Org. Lett. 2000, 2, 469. (q) Rychnovsky, S. D.; Thomas, C. R. Org. Lett. 2000, 2, 1217. (r) Williams, D. R.; Clark, M. P.; Emde, U.; Berliner, M. A. Org. Lett. 2000, 2, 3023. (s) Greer, P. B.; Donaldson, W. A. Tetrahedron Lett. 2000, 41, 3801. (t) Evans, D. A.; Cee, V. J.; Smith, T. E.; Fitch, D. M.; Cho, P. S. Angew. Chem., Int. Ed. 2000, 39, 2533. (u) Huang, H.; Panek, J. S. Org. Lett. 2001, 3, 1693. 10942 J. Am. Chem. Soc. 2001, 123, 10942-10953 10.1021/ja011604l CCC: $20.00 © 2001 American Chemical Society Published on Web 10/13/2001 phorboxazole B (2).7 Herein, we disclose a full account of the total synthesis of (+)-phorboxazole A (1) recently completed in our laboratory.6c A central feature of this synthetic venture was the exploitation of the Petasis-Ferrier rearrangement for the construction of the two 2,6-cis-tetrahydropyran rings resident in the phorboxazole macrolide ring. Petasis-Ferrier Rearrangement. In 1996, Petasis reported that the acid-promoted rearrangement of enol acetals to tetrahydropyranones (e.g., 3f4, Scheme 1) proceeds via fragmentation, followed by endo cyclization onto an oxocarbenium (ii),8 a reaction closely related to the earlier Ferrier Type-II9 enol ether rearrangement (e.g., 5f6) induced by mercuric ion. Inspection of the Petasis-Ferrier rearrangement in the context of complex molecule synthesis revealed two important attributes. First, construction of the enol acetal rearrangement substrates comprises an ideal linchpin tactic for complex fragment assembly; second, the latent element of symmetry inherent in the target cis-tetrahydropyranones permits rearrangement of either enol acetal 8 or 9 (Scheme 2). Both attributes provide considerable latitude for fragment union and thereby cistetrahydropyranone construction. Synthetic Analysis. In addition to the two 2,6-cis-fused tetrahydropyrans (vide supra), the phorboxazoles present a wide array of architectural features, including a 21-membered macrolactone, a trans-fused tetrahydropyran, two oxazoles, and six olefinic units: one Z and two E alkenes, an exomethylene, a diene, and an E-vinyl bromide. From the retrosynthetic perspective (Scheme 3), we envisioned disconnection of the phorboxazoles at C(2-3), C(19-20), and C(28-29) to reveal three subtargets (10, 11, and 12) of comparable structural complexity. In the synthetic sense, fragments 11 and 12 would be united via a Wittig reaction. Continuing with this analysis, disconnection of side chain 10 at C(40-41) and C(32-33) would furnish subtargets 13, 14, and 15. In the forward sense, vinyl stannane 14 and vinyl iodide 13 could be coupled via a Stille reaction. For union of the side chain to the macrocycle, we planned to exploit oxazole triflate 15a,b as a novel bidirectional linchpin (vide infra). Finally, the cornerstone for construction of the central C(20-28) tetrahydropyran, 11, and bistetrahydropyran 12 would be the Petasis-Ferrier rearrangements, respectively, of vinyl acetals 16 and 17. Importantly, the overall synthetic strategy held the promise of considerable flexibility for fragment assembly, their union, endgame operations (vide infra), and the construction of analogues. Bistetrahydropyran 12: The C(3-19) Subtarget. To implement the first Petasis-Ferrier rearrangement, we sought enol acetal 17. Our point of departure entailed preparation of trans-tetrahydropyran 24 from known aldehyde 18 (Scheme 4).10 (6) (a) Smith, A. B., III; Verhoest, P. R.; Minbiole, K. P.; Lim, J. J. Org. Lett. 1999, 1, 909. (b) Smith, A. B., III; Minbiole, K. P.; Verhoest, P. R.; Beauchamp, T. J. Org. Lett. 1999, 1, 913. (c) Smith, A. B., III; Verhoest, P. R.; Minbiole, K. P.; Schelhaas, M. J. Am. Chem. Soc. 2001, 123, 4834. (7) (a) Evans, D. A.; Fitch, D. M. Angew. Chem., Int. Ed. 2000, 39, 2536. (b) Evans, D. A.; Fitch, D. M.; Smith, T. E.; Cee, V. J. J. Am. Chem. Soc. 2000, 122, 10033. (8) Petasis, N. A.; Lu, S.-P. Tetrahedron Lett. 1996, 37, 141. (9) Ferrier, R. J.; Middleton, S. Chem. ReV. 1993, 93, 2779. (10) Evans, D. A.; Kaldor, S. W.; Jones, T. K.; Clardy, J.; Stout, T. J. J. Am. Chem. Soc. 1990, 112, 7001. Scheme 1 Scheme 2 Scheme 3 Total Synthesis of (+)-Phorboxazole A J. Am. Chem. Soc., Vol. 123, No. 44, 2001 10943

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

Abstract: Organomagnesium reagents occupy a central position in synthetic organic and organometallic chemistry. Recently, the halogen-magnesium exchange has considerably extended the range of functionalized Grignard reagents available for synthetic purposes. Functional groups such as esters, nitriles, iodides, imines, or even nitro groups can be present in a wide range of aromatic and heterocyclic organomagnesium reagents. Also various highly functionalized alkenyl magnesium species can be prepared. These recent developments as well as new applications of organomagnesium reagents in cross-coupling reactions and amination reactions will be covered in this Review.

Evolving organic synthesis fostered by the pluripotent phenylsulfone moiety.

Abstract: A comprehensive program for the synthesis of natural (or unnatural) products is analogous to the construction of a pyramid. Careful planning followed by installation of numerous levels of support are required to complete the edifice. Specific “cornerstone” strategies are typically major motivations for undertaking the program. Finally, the venture reflects the desire of the research team to construct a lasting monument to their creativity and hard work (Figure 1). * Corresponding author. E-mail: pfuchs@purdue.edu. Chem. Rev. 2009, 109, 2315–2349 2315

Modulating Reactivity and Diverting Selectivity in Palladium-Catalyzed Heteroaromatic Direct Arylation Through the Use of a Chloride Activating/Blocking Group

Abstract: Through the introduction of an aryl chloride substituent, the selectivity of palladium-catalyzed direct arylation may be diverted to provide alternative regioisomeric products in high yields. In cases where low reactivity is typically observed, the presence of the carbon−chlorine bond can serve to enhance reactivity and provide superior outcomes. From a strategic perspective, the C−Cl bond is easily introduced and can be employed in a variety of subsequent transformations to provide a wealth of highly functionalized heterocycles with minimal substrate preactivation. The impact of the C−Cl functional group on direct arylation reactivity has also been evaluated mechanistically, and the observed reactivity profiles correlate very well with that predicted by a concerted metalation−deprotonation pathway.