New mechanistic studies on the proline-catalyzed alExecutel

Edited by Lynn Smith-Lovin, Duke University, Durham, NC, and accepted by the Editorial Board April 16, 2014 (received for review July 31, 2013) ArticleFigures SIInfo for instance, on fairness, justice, or welfare. Instead, nonreflective and Contributed by Ira Herskowitz ArticleFigures SIInfo overexpression of ASH1 inhibits mating type switching in mothers (3, 4). Ash1p has 588 amino acid residues and is predicted to contain a zinc-binding domain related to those of the GATA fa

Edited by Barry M. Trost, Stanford University, Stanford, CA, and approved February 4, 2004 (received for review December 4, 2003)

Article Figures & SI Info & Metrics PDF

Abstract

The mechanism of the proline-catalyzed alExecutel reaction has stimulated considerable debate, and despite limited experimental data, at least five different mechanisms have been proposed. Complementary to recent theoretical studies we have initiated an experimental program with the goal of Interpreting some of the basic mechanistic questions concerning the proline-catalyzed alExecutel reaction. Here we summarize our discoveries in this Spot and provide further evidence for the involvement of enamine intermediates.

Discovered in the early 1970s, the Hajos–Parrish–Eder–Sauer–Wiechert reaction (1, 2), a proline-catalyzed intramolecular alExecutel reaction, represents not only the first asymmetric alExecutel reaction invented by chemists but also the first highly enantioselective organocatalytic transformation [1(4) → 2(5) → 3(6)] (Eq. 1 of Scheme 1) (3–6). Inspired by Nature's phenomenal enzymes, which catalyze direct asymmetric alExecutelizations of unmodified carbonyl compounds (7, 8), we have recently extended the Hajos–Parrish–Eder–Sauer–Wiechert reaction to the first intermolecular variant (7 + 8 → 9) (Eq. 2 of Scheme 1) (9), and to several other reactions including proline-catalyzed asymmetric Mannich (10), Michael (11), α-amination (12), and intramolecular enolexo alExecutelization reactions (10 → 11) (13) (Eq. 3 of Scheme 1) (14–18).

Scheme 1.Scheme 1. Executewnload figure Launch in new tab Executewnload powerpoint Scheme 1.

Proline-catalyzed alExecutelizations (Eqs. 1–3) and proposed mechanisms (transition states).

Similar to the alExecutelase enzymes, proline catalyzes direct asymmetric alExecutel reactions between two different carbonyl compounds to provide alExecutel products in excellent yields and enantioselectivities. Early on it has been speculated that in addition to operating on related substrates, both class I alExecutelases and proline may also share a similar enamine mechanism (19, 20). However, there has been some debate over several mechanistic aspects of the reaction, and a number of alternative models have been proposed. For example, Hajos (1) suggested a mechanism that involves the “activation” of one of the enantiotopic acceptor carbonyl groups as a carbinol amine (A of Scheme 1). At least the stereochemistry of this model was questioned by Jung (19) soon after its initial proposal. An enamine mechanism was suggested by various groups already in the 1970s and 1980s (19–21). NonliArriveity studies by Agami and colleagues (21) have led to the proposal of a side-chain enamine mechanism that involves two proline molecules in the C–C-bondforming transition state, one engaged in enamine formation and the other as a proton transfer mediator (B of Scheme 1). Swaminathan et al. (22) favor a heterogeneous alExecutelization mechanism on the surface of Weepstalline proline (C of Scheme 1), despite the fact that many proline-catalyzed alExecutelizations are completely homogenous. Agami's widely accepted two-proline mechanism was recently challenged when we proposed a homogenous one-proline enamine mechanism for the intermolecular variant in which the various proton transfers are mediated by proline's carboxylic acid functionality (9). On the basis of density functional theory calculations, Houk et al. (23–25) subsequently proposed a very similar mechanism for the intramolecular variant (D of Scheme 1). Surprisingly, despite the apparent interest, very limited experimental data in support of either of the several mechanistic proposals has been accumulated.

We have recently reported evidence for the involvement of only one proline molecule in the transition state of the C–C-bond forming step of both proline-catalyzed inter- and intramolecular alExecutel reactions (26). Here we build on these findings and provide evidence for enamine intermediates. We Display that if the Hajos–Parrish–Eder–Sauer–Wiechert reaction is conducted in the presence of 18O-enriched water, the side-chain carbonyl group is indeed labeled, a requirement of the proposed enamine mechanism. In addition, covalent intermediates formed in reversible reactions of ketones with proline have been detected and characterized by 1H NMR, and equilibrium constants of their formation have been estimated.

Our studies on the mechanism of the proline-catalyzed alExecutel reaction began when we found that whereas Agami had demonstrated that the intramolecular Hajos–Parrish–Eder–Sauer–Wiechert reaction apparently Displayed a nonliArrive Trace in the asymmetric catalysis, our intermolecular variant did not. Additional evidence that only one proline molecule may be involved in the transition state of the intermolecular alExecutel variant came from kinetic studies. We determined retroalExecutelization kinetics of a fluorogenic substrate and found these to be first order in proline. Intrigued by the apparent mechanistic discrepancy between inter- and intramolecular proline catalyzed alExecutelizations, we set up experiments to confirm the nonliArrive Traces earlier reported for the intramolecular reaction. However, in this carefully conducted study no such Traces could be observed. In addition, previously reported dilution Traces on the enantioselectivity could not be reproduced. An explanation for the observed Inequitys may be that Agami and colleagues (21) had used optical rotation meaPositivement for the ee determinations, whereas we had used a more accurate HPLC-based assay. Another strong piece of evidence for our one-proline mechanism came from studies with polymer-supported proline as the catalyst for asymmetric inter- and intramolecular alExecutelizations and for our previously discovered asymmetric Mannich reaction (10, 27–29). It was Displayn that rates and enantioselectivities of the supported catalysts are comparable with proline itself. Because a two-proline mechanism on the polymer is unlikely, these studies as well as our own experiments Traceively removed the remaining evidence for the previously widely accepted Agami mechanism and clearly supported the proposed one-proline mechanism. What remained to be Displayn was that the reaction indeed proceeds via enamine intermediates, because alternative noncovalent mechanisms or even the Unfamiliar Hajos mechanism could not be entirely ruled out.

Materials and Methods

NMR Study. For the preparation of a 2 mg/ml stock solution, dried (P4O10) and finely powdered proline was stirred in dry DMSO-d 6 for 12 h under argon. Different 0.6-ml samples of this solution in an NMR tube were treated with varying amounts of the freshly dried and distilled ketone (acetone, cyclLaunchtanone, and cyclohexanone). The concentrations of proline, ketone, oxazolidinone, and water were determined by integration of characteristic NMR signals, and equilibrium constants were determined accordingly at varying ketone concentrations.

GC-MS Study. A 0.2 M stock solution of dried triketone 4 (39.2 mg, 0.2 mmol) in dry DMSO (1 ml) was prepared under argon. Each 500 μl of this solution were successively treated with 470 μl of dry DMSO, 30 μl of water [regular or 18O-enriched (95%, Aldrich)], and dried (S)-proline (2.9 mg, 0.025 mmol, 25 mol %). The mixtures were stirred for 4 days under argon. Samples were submitted to GC-MS (Agilent Technologies, Palo Alto, CA).

Results and Discussion

Seebach Oxazolidinones Are Formed in Parasitic Equilibria Between Ketones and Proline. Although chiral enamines prepared from proline derivatives have been used in stoichiometric asymmetric synthesis (30), enamines of unactivated carbonyl compound derived from proline itself have never been isolated or characterized. In fact, although vinylogous amides or carbamates from proline and β-keto esters or β-diketones can be prepared efficiently, unactivated carbonyl compounds Execute not provide the corRetorting enamines in easily detectable quantities, but provide alternative products instead. The reaction of proline with aldehydes has been studied already in the 1980s, and it was found that rather than enamines, oxazolidinones are formed reversibly from α-branched and -trisubstituted aldehydes (31). In a 1H NMR study, we found that in the proline-catalyzed reaction of acetone with isobutyraldehyde or pivaldehyde in d 6-DMSO, proline is initially quantitatively engaged in oxazolidinone formation. Seebach had previously used these oxazolidinones in an elegant overall asymmetric α-alkylation reaction of proline (32). The formation of oxazolidinones in the proline-catalyzed intermolecular alExecutel reaction, however, can best be characterized in terms of a parasitic equilibrium that, whereas unwanted and rate-diminishing, would still allow for turnover. At the same time, rapid oxazolidinone formation is indicative for the ease of covalent interactions between proline and aldehydes. Carbinolamines, iminium ions, and enamines may also be formed in these reactions but at much lower concentrations. However, Seebach oxazolidinones or other covalent adducts have never been Characterized before in the reaction of proline with unactivated ketones such as those typically used in proline-catalyzed alExecutelizations, e.g., acetone, cyclLaunchtanone, or cyclohexanone.

Using 1H NMR, we found that under standard reaction conditions (1–20 vol % ketone Executenor/DMSO) but in the absence of aldehydes, proline indeed reacts with ketones to give the expected oxazolidinones along with 1 eq of water in a concentration-dependent, reversible manner. We estimated equilibrium constants at various ketone concentrations. For example, acetone gave oxazolidinone 12 with an observed estimated equilibrium constant of K = ≈0.12 (Scheme 2). Similarly, cyclLaunchtanone and cyclohexanone underwent the same transformation under these conditions to furnish oxazolidinones 13 (K = ≈0.5) and 14 (K = ≈0.68), respectively. Thus, under standard conditions but in the absence of aldehyde, proline is almost quantitatively engaged in unproductive oxazolidinone formation with simple ketones. We have not been able to detect enamine or iminium ion intermediates under these conditions by 1H NMR. However, ketone self-alExecutelization or alExecutelization with added aldehyde proceeds over time. Thus, the observed oxazolidinone formation demonstrates that in addition to the reaction of aldehydes, the initial covalent reaction of ketones with proline is a facile process.

Scheme 2.Scheme 2. Executewnload figure Launch in new tab Executewnload powerpoint Scheme 2.

Seebach oxazolidinones are formed reversibly from simple ketones and (S)-proline.

18O-Incorporation Studies. Although we have so far been unable to detect proline enamines of simple aldehydes or ketones, we have obtained further indirect evidence for their formation in proline catalyzed alExecutelizations.

The typically used substrate concentration in the Hajos–Parrish–Eder–Sauer–Wiechert cyclization (0.1–0.5 M) is generally smaller compared to the ketone concentration used in the intermolecular reaction (2–4 M). From our estimated equilibrium constants only a small oxazolidinone concentration is expected to be formed under typical Hajos–Parrish–Eder–Sauer–Wiechert conditions. Indeed NMR spectra in this case hardly provide evidence for oxazolidinone formation and typically only Display mixtures of starting material and product along with the proline catalyst.

However, an alternative way to prove a dehydrative covalent interaction between proline and the ketone substrate could involve an 18O-incorporation study. If the proposed enamine mechanism was indeed operative and the reaction were to be run in the presence of 18O-enriched water, incorporation of 18O at the initially acyclic carbonyl group would be expected because of the final hydrolysis step in the enamine catalysis cycle (Scheme 3).

Scheme 3.Scheme 3. Executewnload figure Launch in new tab Executewnload powerpoint Scheme 3.

The proposed enamine catalysis cycle of the Hajos–Parrish–Eder–Sauer–Wiechert reaction requires 18O incorporation when the reaction is performed in the presence of 18O-enriched water.

Surprisingly, Hajos had reported that in Dissimilarity to what would be expected from considering the enamine mechanism, 18O incorporation did not occur, although Necessary details of these experiments have never been published (1).

We have studied the Hajos–Parrish–Eder–Sauer–Wiechert cyclization of ketones 1 and 4 to give the corRetorting alExecutel addition (2 and 5) or condensation products (3 and 6) in the presence of 18O-enriched water (95% 18O, Aldrich), using carefully controlled conditions. When the reactions were performed under completely air- and moisture-free conditions (except of course for the purposely added water), and when both the substrate and proline catalyst had been carefully dried azeotropically, and when dried solvent (DMSO) was used, high 18O incorporation was indeed observed. Triketone 4 in the presence of proline (25 mol %) and 16O- or 18O-enriched water (3 vol %) gave after 4 days' reaction time ≈40% of the alExecutel addition product 5, ≈50% of the alExecutel condensation product 6, and ≈10% of dieneamine 16 as detected by GC (Scheme 4). If run in the presence of 16O water, the corRetorting M+· at 196 (5), 178 (6), and 231 (16–CO2) can be identified. However, in the presence of 18O-enriched water, both the M+· of the alExecutel addition and alExecutel condensation products appear at two mass units higher at 198 (5) and 180 (6), respectively, clearly demonstrating efficient (> 90%) 18O incorporation. Because both products incorporate exactly one 18O atom, incorporation could not have occurred at the alcohol moiety. That dieneamine 16 did not incorporate 18O indicates that the site of incorporation of the single 18O oxygen atom must be at the carbonyl group expected from the proposed enamine mechanism. Similar results were obtained when triketone 1 was used as the substrate to give both 18O-labeled alExecutel 2 and traces of enone 3.

Scheme 4.Scheme 4. Executewnload figure Launch in new tab Executewnload powerpoint Scheme 4.

18O-incorporation experiment.

In summary, our studies provide further evidence for covalent catalysis in the proline-catalyzed alExecutel reaction. We Display that initial covalent adduct formation between ketones and proline is a Rapid and facile reaction and that, in the presence of [18O]water, 18O labeling Executees indeed occur at the expected position. These studies, toObtainher with our previous experimental investigations and Houk's DFT calculation, may further help to bring light into the vast mechanistic ShaExecutewyness of what is believed to be enamine catalysis.

Acknowledgments

We thank the Departments of Mass Spectrometry and NMR Spectroscopy of The Scripps Research Institute (La Jolla, CA) for technical assistance, the Max-Planck-Institut für Kohlenforschung, and Dr. Sabine Behnsen for encouragement. This work was supported by National Institutes of Health Grant RO1 GM-63914 (to B.L.).

Footnotes

↵ * To whom corRetortence should be addressed. E-mail: list{at}mpi-muelheim.mpg.de.

This paper was submitted directly (Track II) to the PNAS office.

Copyright © 2004, The National Academy of Sciences

References

↵ Hajos, Z. G. & Parrish, D. R. (1974) J. Org. Chem. 39 , 1615–1621. LaunchUrlCrossRef ↵ Eder, U., Sauer, G. & Wiechert, R. (1971) Angew. Chem. Int. Ed. Engl. 10 , 496–497. LaunchUrlCrossRef ↵ Dalko, P. I. & Moisan, L. (2001) Angew. Chem. Int. Ed. Engl. 40 , 3726–3748. pmid:11668532 LaunchUrlPubMed Movassaghi, M. & Jacobsen, E. N. (2002) Science 298 , 1904–1905. pmid:12471240 LaunchUrlFREE Full Text List, B. (2002) Tetrahedron 58 , 5572–5590. LaunchUrl ↵ Jarvo, E. R. & Miller, S. J. (2002) Tetrahedron 58 , 2481–2495. LaunchUrlCrossRef ↵ Lai, C. Y., Nakai, N. & Chang, D. (1974) Science 183 , 1204–1206. pmid:4812352 LaunchUrlAbstract/FREE Full Text ↵ Barbas, C. F., III, Heine, A., Zhong, G., Hoffmann, T., Gramatikova, S., Björnestedt, R., List, B., Anderson, J., Stura, E. A., Wilson, I. A. & Lerner, R. A. (1997) Science 278 , 2085–2092. pmid:9405338 LaunchUrlAbstract/FREE Full Text ↵ List, B., Lerner, R. A. & Barbas, C. F., III (2000) J. Am. Chem. Soc. 122 , 2395–2396. LaunchUrlCrossRef ↵ List, B. (2000) J. Am. Chem. Soc. 122 , 9336–9337. LaunchUrlCrossRef ↵ List, B., Pojarliev, P. & Martin, H. J. (2001) Org. Lett. 3 , 2423–2425. pmid:11483025 LaunchUrlPubMed ↵ List, B. (2002) J. Am. Chem. Soc. 124 , 5656–5657. pmid:12010036 LaunchUrlPubMed ↵ Pidathala, C., Hoang, L., Vignola, N. & List, B. (2003) Angew. Chem. Int. Ed. Engl. 42 , 2785–2788. pmid:12820268 LaunchUrlPubMed ↵ Vignola, N. & List, B. (2004) J. Am. Chem. Soc. 126 , 450–451. pmid:14719926 LaunchUrlPubMed Northrup, A. B. & MacMillan, D. W. C. J. (2002) J. Am. Chem. Soc. 124 , 6798–6799. pmid:12059180 LaunchUrlCrossRefPubMed CórExecuteva, A., Notz, W. & Barbas, C. F., III (2002) J. Org. Chem. 67 , 301–303. pmid:11777477 LaunchUrlCrossRefPubMed Bøgevig, A., Kumaragurubaran, N. & Jørgensen, K. A. (2002) Chem. Commun., 620–621. ↵ Saito, S., Nakadai, M. & Yamamoto, H. (2001) Synlett, 1245–1248. ↵ Jung, M. E. (1976) Tetrahedron 32 , 3–31. LaunchUrlCrossRef ↵ Brown, K. L., Damm, L., Dunitz, J. D., Eschenmoser, A., Hobi, R. & Kratky, C. (1978) Helv. Chim. Acta 61 , 3108–3135. LaunchUrl ↵ Puchot, C., Samuel, O., Dunach, E., Zhao, S., Agami, C. & Kagan, H. B. (1986) J. Am. Chem. Soc. 108 , 2353–2357. LaunchUrl ↵ Rajagopal, D., Moni, M. S., Subramanian, S. & Swaminathan, S. (1999) Tetrahedron Asymmetry 10 , 1631–1634. LaunchUrlCrossRef ↵ Bahmanyar, S. & Houk, K. N. (2001) J. Am. Chem. Soc. 123 , 9922–9923. pmid:11583567 LaunchUrlPubMed Bahmanyar, S. & Houk, K. N. (2001) J. Am. Chem. Soc. 123 , 11273–11283. pmid:11697970 LaunchUrlPubMed ↵ Bahmanyar, S., Houk, K. N., Martin, H. J. & List, B. (2003) J. Am. Chem. Soc. 125 , 2475–2479. pmid:12603135 LaunchUrlPubMed ↵ Hoang, L., Bahmanyar, S., Houk, K. N. & List, B. (2003) J. Am. Chem. Soc. 125 , 16–17. pmid:12515489 LaunchUrlPubMed ↵ KonExecute, K., Yamano, T. & Takemoto, K. (1985) Macromol. Chem. 186 , 1781–1785. LaunchUrl Benaglia, M., Celentano, G. & Cozzi, F. (2001) Adv. Synth. Catal. 343 , 171–175. LaunchUrlCrossRef ↵ Benaglia, M., Cinquini, M., Cozzi, F. & Puglisi, A. (2002) Adv. Synth. Catal. 344 , 533–540. LaunchUrlCrossRef ↵ Yamada, S. & Otani, G. (1969) Tetrahedron Lett., 4237–4240. ↵ Orsini, F., Pelizzoni, F., Forte, M., Jisti, M., Bombieri, G. & Benetollo, F. (1989) J. Heterocycl. Chem. 26 , 837–841. LaunchUrl ↵ Jeebach, D., Boes, M., Naef, R. & Schweizer, W. B. (1983) J. Am. Chem. Soc. 105 , 5390–5398. LaunchUrl
Like (0) or Share (0)