Catalysts that can promote acyl transfer processes are important to enantioselective synthesis and their development has received significant attention in recent years. Despite noteworthy advances, discovery of small-molecule catalysts that are robust, efficient, recyclable and promote reactions with high enantioselectivity can be easily and cost-effectively prepared in significant quantities (that is, >10 g) has remained elusive. Here, we demonstrate that by attaching a binaphthyl moiety, appropriately modified to establish H-bonding interactions within the key intermediates in the catalytic cycle, and a 4-aminopyridyl unit, exceptionally efficient organic molecules can be prepared that facilitate enantioselective acyl transfer reactions. As little as 0.5 mol% of a member of the new catalyst class is sufficient to generate acyl-substituted all-carbon quaternary stereogenic centres in quantitative yield and in up to 98:2 enantiomeric ratio (er) in 5 h. Kinetic resolution or desymmetrization of 1,2-diol can be performed with high efficiency and enantioselectivity as well.
N,N-4-dimethylaminopyridine (DMAP) has long been recognized as a uniquely effective and broadly applicable nucleophilic catalyst for a number of important reactions in organic chemistry1. One set of transformations for which DMAP is commonly utilized is the acylation of hydroxyl group in the presence of acid anhydride. The commonly accepted mechanism for this class of reactions, which supported by experimental as well as computational findings, is presented in Fig. 1a (refs 2, 3). The nucleophilic is believed to react first with the acylating agent i to generate N-acylpyridinium salt intermediate ii, which is likely subjected to nucleophilic attack by the alcohol substrate (R2OH) via intermediate iii. A critical feature of this general class of catalytic processes is that the acetate anion that resides within complex ii serves as a Brønsted base to enhance the reactivity of the otherwise relatively mildly nucleophilic hydroxyl unit. Ester product iv and pyridinium salt v are thus formed, and the latter is then neutralized by the stoichiometric base (B; typically Et3N) to re-generate the nucleophilic catalyst. The efficiency with which N-acylpyridinium ion ii is generated4, the Lewis basicity of the counteranion unit as well as the degree to which it remains associated with the positively charged acylating agent (versus loose ion pair) are critical to the facility of the overall transformation5. A number of strategies have been adopted to modulate the effectiveness of acyl transfer agents for which DMAP serves as the parent compound. Among these is the utilization of electronic factors to extend the lifetime of the N-acylpyridinium salt, or by manipulation of conformational effects to enhance electron donation by the amino substituent; there are also instances where a combination of the aforementioned approaches has been adopted (for example, 4-pyrrolidinopyridine (PPY) or 9-azajulolidine)6. A variety of chiral variants, employed for kinetic resolution of alcohol or enantioselective acyl transfer processes, have also been introduced7,8. Such investigations, which have led to the development of various enantiomerically pure promoter molecules that are based on DMAP or PPY scaffolds, as originally put forth by the notable advances reported by Vedejs9 and Fu10, may be classified in four major categories (Fig. 1b–e). One strategy entailed the use of N-acylpyridinium salt with a chiral substituent at the pyridyl ring’s C2 position; however, this structural alteration proved to be detrimental to reaction efficiency, requiring the use of stoichiometric amounts of the catalyst (Fig. 1b)9. A similar approach but involving the C3 site of the heterocyclic ring, has been extensively examined11,12,13,14,15,16,17,18,19. Nonetheless, reactivity levels were again generally reduced, probably as a result of hampering of proper electron donation by the amino substituent, which raises the energy of the critical pyridinium ion intermediates (cf. ii, Fig. 1a)20,21. The issue of diminished catalyst efficiency applies to DMAP or PPY derivatives that carry a ring that connects the C2 and C3 carbons of the pyridyl ring (Fig. 1d)22. In most cases, diminished stability of the key ion-pair intermediate because of steric repulsion between substituents and 4-amino moiety and/or N-acetyl group was a complication21. An exception was the ferrocene-based catalysts developed by Fu et al.23,24; comparatively high catalyst activity and enantioselectivity was observed in a number of different applications. Obtaining this set of chiral catalysts in the enantiomerically pure form, however, requires costly resolution procedures25. The efficiency and considerable longevity of N-acylpyridinium ion has been attributed to the exceptional electron-donating ability of transition metal framework; what’s more, the cyclopentadienyl moiety attached to pyridyl ring is sufficiently small to prevent unfavourable interaction with the N-acetyl and/or the N-dimethyl- and pyrrolidino groups21. Chiral amino derivatives have been positioned at the pyridyl group’s C4 site as well (Fig. 1e)26,27,28,29, but these distally positioned moieties did not generate high degrees of stereochemical differentiation for a wide variety of substrates and, for electronic reasons already mentioned (cf. Fig. 1c), this came at the cost of significant diminution in efficiency. Thus, relatively large substituents are required to construct chiral environment to achieve high enantioselectivity. Another notable concept (dual catalysis/anion-binding approach), which is not classified into aforementioned categories (Fig. 1b–e), was also very effective for enantioselective acyl transfer reactions30,31,32,33,34,35,36,37,38.
According to our continuous efforts for the development of chiral nucleophilic catalysts17,18,19 to design an efficient and highly enantioselective acyl transfer catalyst that can be prepared in significant quantities without the need for expensive and/or specialized techniques, we envisioned chiral DMAP derivatives that might contain a binaphthyl unit at C4 position of a pyridine ring (Fig. 2). We reasoned that this blueprint would have several noteworthy advantages. First, either enantiomeric form of 1,1′-bi-2-naphthol (BINOL) is inexpensively available, thus obviating resolution procedures. Second, the catalyst platform allows synthesis and screening of C1- and C2-symmetric variants from a common intermediate. Third, the proposed catalyst construct easily lends to steric and/or electronic modification through the use of well-established protocols39,40. Finally, the absence of substituents at the C2 or C3 sites of the pyridyl ring (cf. Fig. 1b,c) would ensure that efficiency levels remain high. The suggested line of attack poses several significant challenges, however. One is that because the source of stereogenicity is somewhat distal from the pyridine ring, an attribute can result in minimal enantioselectivity. Thus, appropriate structural modification would be needed if the stereochemical bias inherent in the binaphthyl moiety is to exert a meaningful role in the acyl bond forming event. Towards this end, preliminary examination of molecular models implied that the substituents (functional group) at C3 and C3′ positions of the binaphthyl moiety are located sufficiently proximal to the reaction site, offering an attractive option for influencing enantioselectivity through catalyst structure alteration. Thus, we surmised that attractive interactions (for example, π–π stacking, cation-π affinity27,41 or hydrogen-bonding26) between an appropriate unit within the catalyst structure and counteranion of N-acylpyridinium salt (design option 1, Fig. 2), or the nucleophile (design option 2, Fig. 2) might give rise to enhancement of enantioselectivity and perhaps reaction efficiency. Below, we outline the successful realization of the above plan.
We began by preparing a series of enantiomerically pure DMAP derivatives (1a−p) that contain a 1,1′-binaphthyl unit with different substituents pattern at their C3 and C3′ sites with reference to chiral quaternary ammonium salt syntheses from BINOL (refs 39, 40; Fig. 3a, Supplementary Figs 1–26 and Supplementary Methods). The representative route for synthesis of catalyst 1j is presented in Fig. 3b. Ortho-lithiation of MOM-protected compound 2 derived from (S)-BINOL with n-BuLi, followed by quenching with ethyl chloroformate, and deprotection of MOM group under acidic conditions gave the desired BINOL with 3,3′-diesters 3 in 98% yield over 2 steps (78.9 mmol scale). Then, two hydroxy groups of 3 were converted to the corresponding ditriflate, and subjected to Migita–Kosugi–Stille coupling reaction in the presence of tetra n-butyl ammonium chloride and lithium chloride as additives to afford 5 in 83% yield. Our studies revealed that Migita–Kosugi–Stille coupling reaction using a Pd nanoparticle generated in situ was found to be superior to Negishi coupling reaction40 in large scale reaction because Me2Zn is costly and pyrophoric reagent. The benzylic positions of 5 were brominated using N-bromosuccinimide in the presence of 2,2′-azodiisobutyronitrile to give the desired dibromide 6 in 97% yield. Seven-membered ring formation from dibromide 6 using allylamine gave rise to the formation of amine 7 in 82% yield, and deprotection of ally group afforded amine 8 in 95% yield. Installation of pyridine ring was accomplished by using Buchwald–Hartwig amination of 4-bromopyridine hydrochoride with amine 8 to provide the key intermediate 1e in 70% yield. The formation of bis-tertiary alcohols 1j was readily accomplished by the addition of ArLi to bis-ester 1e in 91% yield. All transformations can be easily carried out in large scale (>10 g scale for 1e from BINOL throughout the whole process, and >1 g scale for 1j from 1e), and overall yield of 1j from (S)-BINOL was 38% (10 steps, >90% average yield for each step) with only 4 times of silica gel column chromatography purifications. The present synthetic route sufficiently secures facile accessibility to the key catalyst. The structures of 1e and 1g were identified by X-ray single-crystal analysis (Supplementary Figs 27 and 28).
Enantioselective steglich rearrangement
With a collection of possible catalysts in hand, we chose Steglich rearrangement1,15,19,34,42,43 of oxindole derivative 9a (Design option 1, Fig. 2) as the model transformation for identifying the optimal promoter molecule. Reactions were performed using 5 mol % of 1a−p in tetrahydrofuran (THF) (0.1 M) at 0 °C for 12 h (Fig. 4a). Reaction with 4-amino pyridine 1a was efficient but generated nearly racemic product (99% conv., 43:57 enantiomeric ratio (er)). Structurally modified versions 1b−f, which contain methoxy, phenyl, 2-naphthyl, carboxyl ester or amide groups at their C3 and C3′ positions were either equally or less efficient than 1a, and were all ineffective in generating 10a with significant enantioselectivity (no more than 72:28 er). The surprising breakthrough came when we evaluated compounds that contain tertiary alcohols unit within their chiral binaphthyl moiety (1g−m); under otherwise identical conditions, use of these catalysts led to the formation of the all-carbon quaternary stereogenic centre not only with exceptional efficiency (>98% conv.) but also in up to 98:2 er. In sharp contrast, C1-symmetric systems, represented by 1n, 1o and 1p proved to be substantially less effective, and afforded nearly racemic mixture of product. Apparently, C2-symmetric scaffold are essential for the establishment of proper enantiofacial discrimination. Subsequent optimization studies (Supplementary Figs 29–38 and Supplementary Tables 1–5), revealed that THF is indeed the optimal solvent and when the transformation is performed at –20 °C with no more than 0.5 mol % 1j, the reaction proceeds to complete conversion within five hours to afford 10a in 98:2 er. Finally, we find that use of 15 g of substrate 9a under the latter conditions (193 mg of 1j) delivers the desired product in quantitative yield (purification by standard silica gel chromatography) and 98:2 er (Fig. 4b, Supplementary Figs 39 and 40); furthermore, catalyst 1j could be recovered in 95% yield, and used in same reaction (0.1 mmol scale) to afford the desired product 10a in >98% yield with 98:2 er without loss of any catalytic activity (Supplementary Fig. 41 and Supplementary Method).
A variety of different substrates can be used in the enantioselective Steglich rearrangement process (Fig. 5 and Supplementary Figs 42–66). Thus, 3-alkyl-, 3-allyl- or 3-propargyl-substituted oxindole products 10b−f were isolated in quantitative yields and in 96:4–99:1 er. Higher catalyst loading (3.0 versus 0.5 mol%) and temperature (25 versus –20 °C) was required in the case of 10c, probably as a result of the presence of the more sterically demanding iso-propyl group. The stereochemical identity of 10c was established through an X-ray structure (Supplementary Fig. 67). Transformation with substrates that contain an alkyl chain that bears a functionalizable polar group, such as an amide (10g), a silyl ether (10h) or a cyano unit (10i) proved to be exceptionally efficient (>98% yield) and highly enantioselective (91:9–97:3 er). Rearrangements involving 3-phenyl- (10j) or 3-thienyl-substituted oxindoles (10k) were more sluggish (3.0 mol % 1j at −20 °C was needed) likely due to their sizeable nature, but were also less enantioselective than the previous examples (79:21–84:16 er). Efficient and enantioselective preparation of bromo-substituted 10l (>98% yield, 92:8 er) and N-Me oxindole 10m (>98% yield, 87:13 er) further illustrates the scope of the catalytic process.
To investigate the mechanism of the catalytic enantioselective rearrangement process, we performed a number of key experiments. First, cross-over studies (Fig. 6) between two marked substrates 9a and 9n clearly indicated that reactions proceed via an ion-pair complex, identifying the recovered starting material 9a and 9n (starting material); 9a′ and 9n′ (scrambled starting material) along with corresponding products 10a, 10n, 10a′ and 10n′ (Supplementary Fig. 68)44. Second, we carried out kinetic measurements (Fig. 7) with transformations promoted by catalyst 1j, the corresponding bis-methyl ether 1j′, and DMAP; oxindole 9a served as the substrate under the optimal conditions (0.5 mol% catalyst, THF (0.4 M), −20 °C, 5 h). In all cases, the reactions were found to be first-order with respect to the substrate (Supplementary Table 6). Moreover, substantially higher activity was observed with catalyst 1j (k1j=1.22 h−1) versus its derived bis-methyl ether 1j′ (k1j′=2.62 × 10−2 h−1), or DMAP (kDMAP=7.47 × 10−2 h−1). Thus, acyl rearrangement was nearly 50 times faster with 1j compared with 1j′ and 16 times faster than DMAP. Additionally, whereas the desired product was obtained in 98:2 er when 1j was use, there was hardly any enantiofacial selectivity when the hydroxyl units were protected (66:34 er with 1j′). The presence of tertiary alcohols clearly has a significant impact on the rate as well as enantioselectivity of the catalytic process.
To gain further insight regarding the role of the chiral catalyst’s tertiary hydroxyl groups, density functional theory (DFT) calculations were performed at the B3LYP/6-31G(d) level, with 9a as the substrate and compound 1g as the catalyst, which represent simplified catalyst of 1j. These investigations point to two critical attractive interactions, which directly involve the tertiary alcohol moiety, between the chiral catalyst and tight ion-pair intermediate. In the lowest energy transition state TS-I (Fig. 8 and Supplementary Table 7), which consistent with the experimental observations leads to the observed major enantiomer, there appears to be an H-bonding between the enolate oxygen of the ion pair and the catalyst’s hydroxy unit; it is likely that the conformational rigidity imposed by the presence of the two aryl unit on the same carbon, forces the hydroxyl unit to be properly positioned to associate with the negatively charged oxygen. Additionally, there appears to be an additional electrostatic attraction45,46 between the enolate and an ortho hydrogen of one of the aforementioned aryl units at the C3 site of the chiral catalyst. The second lowest mode of addition, as indicated by DFT calculations, is transition state II (Fig. 8 and Supplementary Table 8). While there appears to be similar electrostatic attractive forces operative here as well, II seems to suffer from a significant steric repulsion between the substrates phenoxy unit and the backbone of the catalyst’s biaryl moiety. Nevertheless, DFT calculations indicate that there is in all likelihood steric repulsion between phenyl unit and the tertiary hydroxyl fragment that is involved in attractive interactions with the enolate group (see transition state (TS)-I, Fig. 8); this is supported by the findings that a catalyst with meta-(3,5)-substituted aryl groups give lower enantioselectivities in the reaction of 9a (cf. 1l or 1m in Fig. 4). Further, as indicated by the transformation that afforded 10m (Fig. 5) involving a more diminutive N-Me group, while less enantioselective than when a benzoate group is present (9a), there is still appreciable enantiofacial differentiation observed (98:2 er versus 87:13 er for 10a and 10m, respectively). This suggests that other, non-steric, factors are at play here as well. Towards this end, second order perturbation theory analysis in NBO at the M062X/6-31g** level indicates that C–H/enolate attraction might be notably stronger in the favoured TS-I (Supplementary Table 8).
The scope of the reaction
The utility of the present class of catalysts is not confined to Steglich rearrangements. For examples, as the representative data in Fig. 9 indicate, we find that binaphthyl-based DMAP derivatives with tert-alcohols at 3,3′-positions of a 1,1′-binaphthyl unit is not only effective in kinetic resolution of secondary carbinol and d,l-1,2-diol but in enantioselective desymmetrization of meso-1,2-diol as well. Initially, kinetic resolution of secondary carbinol rac-11 with an array of binaphthyl-based DMAP derivatives was performed. The reaction in the presence of 5 mol % 1j proceeded smoothly with moderate s-factor (s=11, Fig. 9a, and Supplementary Figs 69–72). We then turned our attention to 1,2-diol which might be more suitable than simple carbinols, expecting positive interactions between a substrate and a catalyst through the hydrogen bonding.
Its merits note that, although a number of organocatalysts for kinetic resolution and desymmetrization of 1,2-diol have been disclosed, the significant majority involve the use of cyclic substrates because enantioselectivity was usually high compared with acyclic substrate8. The successful organocatalytic approaches with high enantioselectivity for kinetic resolution47 and desymmetrization48,49 of acyclic 1,2-diols were only reported by Fujimoto utilizing cinchona alkaloids-based catalyst. However, higher catalyst loading (30 mol %) were required for these transformation. Other examples for desymmetrization of acyclic meso-1,2-diols resulted in moderate enantioselectivity of mono-acylated product along with significant amount of undesired bis-acylated product14,50,51,52. Thus, an efficient resolution (s=125) of d,l-1,2-diol 13 was observed in an acylation reaction promoted by 0.5 mol % 1g performed in THF at −78 °C for 9 h (Fig. 9b and Supplementary Figs 73–76). None of the di-acylation product was observed. Furthermore, desymmetrization of acyclic meso-1,2-diol 15 required only 0.1 mol% 1g and proceeded to furnish the desired mono-ester 16 in 79% yield with 97:3 er along with small amount of di-acylated product 17 and recovered meso-15 in 7% and 12% yield, respectively (Fig. 9c and Supplementary Figs 77 and 78). The substantially faster rate of the first acylation reaction points to a high degree of catalyst-substrate molecular recognition that might be largely due to precise arrangements that are required for the type of H-bonding interactions depicted for ‘design option 2’ in Fig. 2. These preliminary results regarding enantioselective acylation processes, along with the aforementioned Steglich rearrangement reactions, suggest that the present set of catalysts may be applicable to a broad range of acyl transfer-type process.
The studies described above illustrate that the combination of a binaphthyl moiety, a widely utilized chiral motif in enantioselective catalysis, a 4-aminopyridine, a most effective nucleophilic catalyst, can be effectively used in the development of exceptionally effective small organic molecules that can serve as chiral catalysts for acyl transfer processes. Another crucial design element relates to the presence of suitably positioned hydroxy groups that can facilitate reaction and promote enantioselectivity by establishing electrostatic association with an anionic Lewis basic fragment. The need for incorporation of additional substituents within the pyridyl ring, which can cause significant lowering of catalyst activity, may therefore be obviated. With the present blueprint in hand, development of highly efficient and selective catalysts that belong to the same class and may be used for related transformations such as intermolecular phosphorylation53, silylation54,55,56,57,58 or tosylation59 of polyhydroxylated organic molecules may be envisioned. Investigations along these lines are now underway.
General procedure fur enantioselective Steglich rearrangement under optimal conditions
A solution of the catalyst in THF (50.0 mM) was prepared in advance using the following reaction.
To a solution of substrate 9 (0.2 mmol) in THF (0.5 ml, 0.4 M) was added a solution of the catalyst (20 μl, 50 mM in THF) at −20 °C. The reaction mixture was stirred for 5 h and then 1 M aqueous HCl was added. The resulting mixture was extracted with EtOAc, dried over MgSO4 and concentrated in vacuo. The purification of the crude product by flash column chromatography on a short pad of silica gel (eluent:hexane/Et2O=1/1, v/v) gave the corresponding product 10 (>98% yield). For nuclear magnetic resonance and high-performance liquid chromatography analyses of the products, see the Supplementary Figs 39–41 and 43–66.
Accession codes: The X-ray crystallographic coordinates for structures reported in this study have been deposited at the Cambridge Crystallographic Data Centre (CCDC), under deposition numbers CCDC 1432805–1432807. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
How to cite this article: Mandai, H. et al. Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions. Nat. Commun. 7:11297 doi: 10.1038/ncomms11297 (2016).
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This research was partially supported by a Grant-in-Aid for Scientific Research on Innovative Areas ‘Advanced Molecular Transformations by Organocatalysts’ from MEXT (Japan). We thank the Division of Instrumental Analysis, Department of Instrumental Analysis & Cryogenics, Advanced Science Research Center, Okayama University for nuclear magnetic resonance (NMR), high-resolution mass spectrometry measurements (FAB) and X-ray single crystal structural analyses. Some of this work (ESI) was conducted at Institute of Transformative Bio-Molecules (WPI-ITbM) at Nagoya University. The authors are also grateful to Professor Dr Amir, H. Hoveyda (Boston College) for discussions and critical comments on this manuscript.
The authors declare no competing financial interests.
Supplementary Figures 1-78, Supplementary Tables 1-8, Supplementary Methods and Supplementary References (PDF 7846 kb)
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Mandai, H., Fujii, K., Yasuhara, H. et al. Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions. Nat Commun 7, 11297 (2016). https://doi.org/10.1038/ncomms11297
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