Article | Open | Published:

Catalytic enantioselective oxidative coupling of saturated ethers with carboxylic acid derivatives

Nature Communicationsvolume 10, Article number: 559 (2019) | Download Citation


Catalytic enantioselective C–C bond forming process through cross-dehydrogenative coupling represents a promising synthetic strategy, but it remains a long-standing challenge in chemistry. Here, we report a formal catalytic enantioselective cross-dehydrogenative coupling of saturated ethers with diverse carboxylic acid derivatives involving an initial oxidative acetal formation, followed by nickel(II)-catalyzed asymmetric alkylation. The one-pot, general, and modular method exhibits wide compatibility of a broad range of saturated ethers not only including prevalent tetrahydrofuran and tetrahydropyran, but also including medium- and large-sized cyclic moieties and acyclic ones with excellent enantioselectivity and functional group tolerance. The application in the rapid preparation of biologically active molecules that are difficult to access with existing methods is also demonstrated.


The cross-dehydrogenative coupling (CDC) of two readily available C–H components has emerged as a powerful approach for C–C bond construction whereby the only loss is H2 formally1,2,3. The design of the catalytic asymmetric variant is particularly attractive, but remains a challenging task4,5,6. Although impressive progress has been made in enantioselective CDC during the last decade, current studies predominantly focused on N-arylated amine7,8,9,10,11,12,13,14,15,16,17,18,19 and xanthese substrates20,21,22,23,24,25. In contrast, enantioselective CDC of ethers has remained scarce, and the unique existing two examples still focused on specific, activated benzylic and allylic ethers26,27. Our group described an enantioselective bimolecular CDC of cyclic benzylic ethers and aldehydes with high enantioselectivity26. Scheidt reported a delicate asymmetric intramolecular CDC of allylic ethers with appended β-keto esters, providing substituted tetrahydropyran-4-ones with excellent diastereo- and enantioselectivities27. On the other hand, optically pure saturated ethers with diverse α-alkyl substitutions represent ubiquitous structural motifs in numerous bioactive natural products and synthetic pharmaceuticals28,29,30. However, each catalytic asymmetric method is typically suitable for a single class of tetrahydrofuran (THF), tetrahydropyran (THP), or acyclic ether skeleton with a specific α-alkyl substitution pattern31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46. A general and modular catalytic enantioselective method to rapidly access saturated ethers with diverse skeletons and α-alkyl substituent patterns from readily available starting materials has remained elusive. Diverse saturated ether skeletons are basic feedstocks, and many of which, such as THF, THP, and diethyl ether, are daily used solvents in both academia and industry. Therefore, the development of catalytic asymmetric synthetic method starting from such abundant, low value chemical resources and sp3 C–H components is highly desirable. Herein, we report a formal catalytic enantioselective CDC of saturated ethers and carboxylic acid derivatives. The one-pot method exhibits wide compatibility of a broad range of saturated cyclic and acyclic ethers with excellent enantioselectivity. The application in the rapid preparation of biologically active molecules that are difficult to access with existing methods has also been demonstrated.


Reaction design

Presumably, two major challenges hamper the design of catalytic asymmetric oxidative coupling starting from saturated ethers. First, due to the low reactivity of saturated ethers, the C–H cleavage process requires strongly oxidative conditions, making the compatibility with delicate asymmetric catalysis system difficult to achieve47. Second, while catalytic asymmetric addition to aromatic oxocarbenium ions has received considerable attentions48,49,50,51,52,53, the lack of any site on non-aromatic oxocarbenium ions for substrate–catalyst interactions makes asymmetric synthesis of α-substituted saturated ethers via such intermediates remains elusive54,55,56. Herein, we communicate a one-pot catalytic asymmetric synthetic method involving a broad range of saturated ethers and diverse carboxylic acid derivatives as starting materials. The one-pot synthetic method was designed as follow: saturated ether reacting with a combination of a protic additive and peroxide furnished a racemic acetal, which then ionized to corresponding oxocarbenium intermediate for enantioselective C–C bond forging process.

Reaction condition optimization

The reaction of THF (1a) and acetyloxazolidinone 2a was selected for optimization using bisoxazoline L1/Mg(ClO4)2 as chiral catalyst (Table 1)57,58,59,60,61. An initial survey revealed that oxidation of THF with hexanoic acid proceeded smoothly in the presence of tBuOOH and a suitable additive, including TBAI, Fe(acac)3, Cu(acac)2, Cu(OAc)2, and CuOAc62. However, these catalytic amount of additive exhibited a dramatic effect on the subsequent enantioselective C–C bond forming reaction in the presence of BF3·OEt2/2,4,6-collidine, and CuOAc was identified to be optimal, providing expected 3a in 14% yield with 17% ee as a separable mixture of diastereomers (d.r. = 50:50) (entries 1–5, Table 1). Lowing the loading of CuOAc afforded an improved reaction efficiency and ee (entry 6, Table 1). Acetyloxazolidinethione 2aa proved to be a better component with regard to ee and yield (entry 7, Table 1). An extensive investigation of the combination of Lewis acid with chiral ligands L1-L6 revealed that diphosphine L6 and Ni(OTf)2 provided the highest yields and enantiocontrol (entries 8–17, Table 1). By using pre-prepared L6·Ni(OTf)2 as catalyst, the yield increased from 55% to 61% without detriment to ee (entry 18, Table 1). By increasing the loading of BF3·OEt2, the enantioselectivity and yield were improved to 90% and 86%, respectively (entry 19, Table 1). The reaction was also highly dependent on the solvent choice, and the nucleophilic addition stage worked the best in a mixed THF/CH2Cl2 (entry 20, Table 1). The effect of protic additives was further explored, and reaction with PhCOOH furnished the product in 81% yield and 98% ee as a 67:33 mixture of diastereomers, which were separable through silica gel chromatography (entry 21, Table 1). The combination of BF3·OEt2/2,4,6-collidine proved to be crucial to the expected reactivity (See Supplementary Table 1). No desired product was detected when BF3·OEt2 was replaced with TMSOTf or 2,4,6-collidine with diisopropylethylamine. Lowering the reaction temperature for the asymmetric C–C bond forming process did not provide any improvement on the diastereoselectivity (entry 22, Table 1).

Table 1 Reaction condition optimizationa

Scope of acetic acid derivatives

The scope of acetic acid derivatives was then explored (Fig. 1). A variety of electron-donating and -withdrawing substituents at the ortho-, meta-, and para-positions of the aryl ring were well compatible with the reaction conditions, providing respective α-aryl acetamide substituted THF 3a3l in good yields with moderate diastereoselectivity and excellent enantioselectivity (93–98% ee) for both isomers. (α-Heteroaryl) 3o, as well as (α-nathphyl)acyl oxazolidinethiones 3m and 3n were suitable components in high enantioselectivities. N-phenylacyl thiazolidinethione was also well tolerated, as demonstrated by the generation of 3p in 96% ee.

Fig. 1
Fig. 1

The scope of α-aryl acetic acid derivatives. Conditions: PhCOOH (0.5 mmol, 2.5 equiv), CuOAc (2.5 mol%), tBuOOH in decane (2.5 equiv) in THF (1.0 mL) at 80 °C for 2 h, followed by 2 (1.0 equiv), L6·Ni(OTf)2 (10 mol%), 2,4,6-collidine (3.0 equiv) and BF3·OEt2 (4.0 equiv) in THF/CH2Cl2 (0.3 mL/0.1 mL) at rt for 2 h

To further expand the synthetic utility of the method, we next investigated the possibility of α-alkenyl acetic acid derivatives as coupling components (Fig. 2). Thiazolidinethione 3r was superior to oxazolidinethione 3q in terms of ee and yield. In general, the reaction exhibited excellent regioselectivity, and the alkylation occurred exclusively at the α-position of 3-butenoyl derivatives with olefin geometry highly conserved. Electronically varied γ-aryl substituted 3-butenoyl 2s and 2t together with γ-alkyl substituted 2u2x were competent components, providing corresponding 3s3w in good yields with 90–96% ee. γ-Disubstituted 2y and 2z were also well tolerated in excellent enantiocontrol. The method had an excellent functional group tolerance, with common functionalities including terminal alkyne (3ba), benzoate (3bb), silyl ether (3bc), halide (3bd), and azide (3be) well tolerated in 90–92% ee for further manipulation. No expected product 3bf was observed when α-alkyl acetic acid derivative 2bf was used as the coupling partner.

Fig. 2
Fig. 2

The scope of α-alkenyl acetic acid derivatives. Conditions: PhCOOH (0.5 mmol, 2.5 equiv), CuOAc (2.5 mol%), tBuOOH in decane (2.5 equiv) in THF (1.0 mL) at 80 °C for 2 h, followed by 2 (1.0 equiv), L5·Ni(OTf)2 (10 mol%), 2,4,6-collidine (3.0 equiv), and BF3·OEt2 (4.0 equiv) in CH3CO2CH3/CH2Cl2 (0.3 mL/0.1 mL) at rt for 2 h

Scope of saturated ethers

The scope of saturated cyclic ethers was next examined (Fig. 3). Under the standard conditions, 1,1-disubstituted THF proved to be competent substrates, furnishing trisubstituted THF 4a4c in good yields with 94–96% ee and moderate d.r.. Enantioselective reaction of THP with α-aryl and α-vinyl substituted acetic acid derivatives also proceeded smoothly, giving corresponding 4d4j with excellent enantiocontrol. The success in the prevalent THF and THP frameworks encouraged us to further investigate the feasibility of enantioselective functionalization of larger cyclic ethers. Delightedly, medium-sized cyclic, aliphatic ethers, such as oxepane and oxocane, were tolerated, providing 4k and 4l in 96% ee and 92% ee, respectively. Albeit slightly decreased efficiency, large-sized cyclic, saturated ethers were also identified as competent substrates, as demonstrated by the generation of 13-membered 4m and 16-membered 4n in 96% ee and 95% ee. Although the scope of saturated cyclic ethers was not exclusively investigated, these results provide a proof-of-concept for the generality and modularity of the asymmetric synthetic method.

Fig. 3
Fig. 3

The scope of cyclic saturated ethers. Conditions: PhCOOH (0.5 mmol, 2.5 equiv), CuOAc (2.5 mol%), tBuOOH in decane (3.0 equiv) in ether (1.0 mL) at 80 °C for 6–12 h, followed by 2 (1.0 equiv), L5·Ni(OTf)2 or L6·Ni(OTf)2 (10 mol%), 2,4,6-collidine (3.0 equiv), and BF3·OEt2 (4.0 equiv) in CH2Cl2 (0.4 mL) at rt for 2 h

The tolerance of large-sized, cyclic ether prompted us to further explore the generality of the method for acyclic saturated ethers (Fig. 4). Pleasingly, enantioselective reaction of commonly used solvents, such as diethyl ether, dipropyl ether, and dibutyl ether, with 2aa proceeded smoothly, providing 6a6c in good yields with 90–94% ee. Aside from symmetric acyclic ethers, unsymmetric ones also proved to be suitable substrates, as demonstrated by the highly enantioselective reaction of methyl n-butyl ether (6d) and methyl n-hexyl ether (6e). The reaction exhibited excellent regioselectivity, and no substitution at primary C–H bond was observed. Acyclic ethers bearing a variety of commonly encountered functional groups, such as ether (6f), halide (6g), and acetate (6h), were also well tolerated for further manipulation. No improvement on the diastereoselectivity was observed when bulky tert-butyl ethyl ether (6i) was employed.

Fig. 4
Fig. 4

The scope of acyclic saturated ethers. Conditions: PhCOOH (0.5 mmol, 2.5 equiv), CuOAc (2.5 mol%), tBuOOH in decane (3.0 equiv) in ether (1.0 mL) at 80 °C for 6–12 h, followed by 2 (1.0 equiv), L6·Ni(OTf)2 (10 mol%), 2,4,6-collidine (3.0 equiv), and BF3·OEt2 (4.0 equiv) in CH2Cl2 (0.4 mL) at rt for 2 h

Synthetic applications

The synthetic utilities of the method was next explored (Fig. 5). First, the oxa- and thiazolidinethione moieties can be readily converted to other synthetically valuable functional groups. For example, the adduct 3a was converted to corresponding alcohol 7, ester 8, thioester 9, and Weinreb amide 10 in high efficiency with the ee highly conserved (Fig. 5a). Enantiopure diastereomers 12a and 12b are potent and selective dopamine transporter inhibitors (Fig. 5b)63. However, traditional synthetic method, which relied on menthol or 1-indanol mediated resolution technology, required seven steps for each isomer preparation starting from 3,4-dihydro-2H-pyran. Our method exhibited moderate diastereoselectivity, which afforded an opportunity to rapidly access both 12a and 12b in excellent ee through a two-step process consisting of asymmetric reaction of THP (1d) with 11 and esterification. Second, given the tolerance of a broad range of carboxylic acid derivatives, we envisioned that removing the exocyclic stereocenter would further enhance the synthetic utility of the protocol. Therefore, we designed a concise two-step sequence involving DIBAL-H mediated reduction of oxa- or thiazolidinethione to aldehyde followed by Ru(PPh3)3Cl catalyzed decarbonylation, providing α-alkyl substituted saturated ethers 1317 that are difficult to prepare by other methods (Fig. 5c).

Fig. 5
Fig. 5

Synthetic utilities. a Transformations of oxa- and thiazolidinethiones to other synthetically valuable functional groups. b Rapid synthesis of two dopamine transporter inhibitors. c Removal of the oxa- and thiazolidinethione moieties


Control experiments were conducted to gain a preliminary understanding of the reaction mechanism (Fig. 6). First, in the presence of CuOAc and tBuOOH, THF (1a) reacted with PhCO2H giving acetate 18 in 88% yield (Fig. 6a). Subjecting 18 to the standard condition furnished expected 3aa with comparable results to that observed in the reaction starting from THF (1a) (Fig. 6b). The observations implied the intermediacy of 18 in the process. Second, the alkylation of 18 with 2aa proceeded smoothly under the standard reaction condition in the absence of oxidation elements (Fig. 6c). No expected 3aa was observed when the combination of L6 and CuOAc was used as the catalyst (Fig. 6d). These results suggested that the species binding to diphosphine ligand should be Ni(OTf)2 but not CuOAc.

Fig. 6
Fig. 6

Mechanistic studies. a Reaction intermediate identification. b Asymmetric coupling of 18 with 2aa. c Asymmetric coupling of 18 with 2aa in the absence of CuOAc. d Identification of the real metal catalyst for the asymmetric coupling

Based on the above observations, a plausible catalytic cycle is outlined in Fig. 7. Carboxylic acid derivative 2aa coordinates with L6·Ni(OTf)2 complex giving rise to 19, in which the acidity of the hydrogen α to the carbonyl moiety increases. 2,4,6-Collidine promotes the enolization of 19 providing chiral Ni-bound Z-enolate 2064. 20 Reacts with cyclic oxocarbenium 21 generated in situ from acetal 18 and BF3·OEt2 yielding 22. Product dissociation completes the catalytic cycle. Notably, no reactivity was detected when diisopropylethylamine was used instead of 2,4,6-collidine, indicating that the role of latter might not simply act as a base. Fujioka and Kita reported that in the presence of a suitable Lewis acid, the acetal reacted with 2,4,6-collidine furnishing corresponding pyridinium-type salt65. During our in situ 1H NMR study of the mixture of acetal 18, BF3·OEt2, and 2,4,6-collidine, a peak at δ ~ 6.4 ppm was observed, which is characteristic for such type of pyridinium species65,66. Accordingly, we envisioned that 2,4,6-collidine might react with oxocarbenium 21 reversibly furnishing pyridinium 23. Adduct 23 possessing weak electrophilicity might be considered as a reservoir of 21 to prevent the decomposition before the capture by enolate 20.

Fig. 7
Fig. 7

A proposed catalytic cycle. The possible reaction pathway based on our studies and previous literature

The stereochemical induction model based on the Ni-bound Z-enolate with chiral bidentate phosphine ligand L6 (MeO-BIPHEP) was proposed in Fig. 8. The P-bound phenyl group on the ligand (in red) shields the top face (Re face) of the enolate substrate (in blue), which disfavors the electrophilic attack by the oxocarbenium intermediate. In contrast, the addition of the oxocarbenium ion to the Si face of the enolate substrate is favored due to less repulsive interactions with the ligand. This model is consistent with the experimentally observed stereochemistry. The low to moderate diastereoselectivity observed for saturated ethers might be ascribed to the lack of Lewis basic site on corresponding oxocarbenium ion intermediates for substrate–catalyst interactions.

Fig. 8
Fig. 8

Stereochemical induction model with chiral Ni-bound Z-enolate. The geometry was optimized at the B3LYP/LANL2DZ–6–31G(d) level

In summary, a one-pot catalytic enantioselective reaction of saturated ethers with diverse carboxylic acid derivatives is described. The general and modular method exhibits wide compatibility of a broad range of saturated cyclic ethers not only including prevalent THF and THP, but also including medium- and large-sized cyclic moieties with excellent enantioselectivity and functional group tolerance. The generality of the method is further demonstrated by application in saturated acyclic ethers. The synthetic application in the rapid preparation of biologically active molecules that are difficult to access with existing methods is demonstrated. We envision that the general, modular, and highly enantioselective reaction of abundant, low value saturated ethers outlined herein will provide a topologically straightforward synthetic planning for both complex target molecules and a plethora of analogs for lead discovery and optimization.


General procedure for the reaction of THF (1a) with 2aa

In an oven-dried Teflon septum screw-capped tube, PhCOOH (61 mg, 0.5 mmol), CuOAc (0.6 mg, 0.005 mmol, 2.5 mol%), and tBuOOH in decane (0.5 mmol) were added to THF (1.0 mL). The solution was stirred at 80 °C for 2 h before the solvent was evaporated. Then carboxylic acid derivative 2aa (44.3 mg, 0.2 mmol), L6·Ni(OTf)2 (18.7 mg, 0.02 mmol), 2,4,6-collidine (79.3 μL, 0.6 mmol), and BF3·OEt2 (98.7 μL, 0.8 mmol) in THF/CH2Cl2 (0.3 mL/0.1 mL, v-v) was added. After stirring at rt for 2 h, solvents were removed and the residue was purified by silica gel column chromatography (CH2Cl2/ethyl acetate = 99:1) giving the expected 3aa in 81% yield (47.2 mg) with 98% ee as a separable mixture of diastereomers (d.r. = 2:1).

Data availability

The authors declare that the data supporting the findings of this study are available within the article and its Supplementary Information files. The X-ray crystallographic coordinates for structures reported in this article have been deposited at the Cambridge Crystallographic Data Center (3p: CCDC 1858037, 3p’: CCDC 1858065, 3s: CCDC 1858049, 4e: CCDC 1858043, 4l: CCDC 1890776). These data could be obtained free of charge from The Cambridge Crystallographic Data Center via

Additional information

Journal peer review information Nature Communications thanks Lei Gong, Doron Pappo, and the other anonymous reviewer for their contribution to the peer review of this work.

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.


  1. 1.

    Li, C.-J. Cross-dehydrogenative coupling (CDC): exploring C–C bond formations beyond functional group transformations. Acc. Chem. Res. 42, 335–344 (2009).

  2. 2.

    Girard, S. A., Knauber, T. & Li, C.-J. The cross-dehydrogenative coupling of Csp3–H bonds: a versatile strategy for C–C bond formations. Angew. Chem. Int. Ed. 53, 74–100 (2014).

  3. 3.

    Liu, C., Zhang, H., Shi, W. & Lei, A. Bond formations between two nucleophiles: transition metal catalyzed oxidative cross-coupling reactions. Chem. Rev. 111, 1780–1824 (2011).

  4. 4.

    Zheng, C. & You, S.-L. Recent development of direct asymmetric functionalization of inert C–H bonds. RSC Adv. 4, 6173–6214 (2014).

  5. 5.

    Qin, Y., Lv, J. & Luo, S. Catalytic asymmetric α-C (sp3)–H functionalization of amines. Tetrahedron Lett. 55, 551–558 (2014).

  6. 6.

    Yang, L. & Huang, H. Asymmetric catalytic carbon–carbon coupling reactions via C–H bond activation. Catal. Sci. Technol. 2, 1099–1122 (2012).

  7. 7.

    Li, Z. & Li, C.-J. Catalytic enantioselective alkynylation of prochiral sp3 C−H bonds adjacent to a nitrogen atom. Org. Lett. 6, 4997–4999 (2004).

  8. 8.

    Tan, Y., Yuan, W., Gong, L. & Meggers, E. Aerobic asymmetric dehydrogenative cross-coupling between two C–H groups catalyzed by a chiral-at-metal rhodium complex. Angew. Chem. Int. Ed. 54, 13045–13048 (2015).

  9. 9.

    Zhang, J., Tiwari, B., Xing, C., Chen, X. & Chi, Y. R. Enantioselective oxidative cross-dehydrogenative coupling of tertiary amines to aldehydes. Angew. Chem. Int. Ed. 51, 3649–3652 (2012).

  10. 10.

    Zhang, G., Zhang, Y. & Wang, R. Catalytic asymmetric activation of a Csp3–H bond adjacent to a nitrogen atom: a versatile approach to optically active α-alkyl α-amino acids and C1-alkylated tetrahydroisoquinoline derivatives. Angew. Chem. Int. Ed. 50, 10429–10432 (2011).

  11. 11.

    Zhang, G., Ma, Y., Wang, S., Zhang, Y. & Wang, R. Enantioselective metal/organo-catalyzed aerobic oxidative sp3C–H olefination of tertiary amines using molecular oxygen as the sole oxidant. J. Am. Chem. Soc. 134, 12334–12337 (2012).

  12. 12.

    DiRocco, D. A. & Rovis, T. Catalytic asymmetric α-acylation of tertiary amines mediated by a dual catalysis mode: N-heterocyclic carbene and photoredox catalysis. J. Am. Chem. Soc. 134, 8094–8097 (2012).

  13. 13.

    Neel, A. J., Hehn, J. P., Tripet, P. F. & Toste, F. D. Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids. J. Am. Chem. Soc. 135, 14044–14047 (2013).

  14. 14.

    Liu, X., Meng, Z., Li, C., Lou, H. & Liu, L. Organocatalytic enantioselective oxidative C–H alkenylation and arylation of N-carbamoyl tetrahydropyridines and tetrahydro-β-carbolines. Angew. Chem. Int. Ed. 54, 6012–6015 (2015).

  15. 15.

    Wei, G. et al. Enantioselective aerobic oxidative C(sp3)–H olefination of amines via cooperative photoredox and asymmetric catalysis. ACS Catal. 6, 3708–3712 (2016).

  16. 16.

    Shang, M. et al. C–H functionalization of amines via alkene-derived nucleophiles through cooperative action of chiral and achiral Lewis acid catalysts: applications in enantioselective synthesis. J. Am. Chem. Soc. 140, 10593–10601 (2018).

  17. 17.

    Yang, Q. et al. Visible-light-promoted asymmetric cross-dehydrogenative coupling of tertiary amines to ketones by synergistic multiple catalysis. Angew. Chem. Int. Ed. 56, 3694–3698 (2017).

  18. 18.

    Zhou, G., Liu, F. & Zhang, J. Enantioselective gold-catalyzed functionalization of unreactive sp3 C–H bonds through a redox-neutral domino reaction. Chem. Eur. J. 17, 3101–3104 (2011).

  19. 19.

    Milo, A., Neel, A. J., Toste, F. D. & Sigman, M. S. A data-intensive approach to mechanistic elucidation applied to chiral anion catalysis. Science 347, 737–743 (2015).

  20. 20.

    Benfatti, F., Guiteras Capdevila, M., Zoli, L., Benedetto, E. & Cozzi, P. G. Catalytic stereoselective benzylic C–H functionalizations by oxidative C–H activation and organocatalysis. Chem. Commun. 45, 5919–5921 (2009).

  21. 21.

    Guo, C., Song, J., Luo, S. W. & Gong, L. Z. Enantioselective oxidative cross-coupling reaction of 3-indolylmethyl C–H Bonds with 1, 3-dicarbonyls using a chiral lewis acid-bonded nucleophile to control stereochemistry. Angew. Chem. Int. Ed. 49, 5558–5562 (2010).

  22. 22.

    Cao, W. et al. Catalytic asymmetric cross-dehydrogenative coupling: activation of C–H bonds by a cooperative bimetallic catalyst system. Chem. Commun. 49, 3470–3472 (2013).

  23. 23.

    Deng, T., Wang, H. & Cai, C. Copper-catalyzed asymmetric oxidative cross-coupling of 2-naphthols with aryl methyl ketones. Eur. J. Org. Chem. 2015, 1569–1574 (2015).

  24. 24.

    Narute, S. & Pappo, D. Iron phosphate catalyzed asymmetric cross-dehydrogenative coupling of 2-naphthols with β-ketoesters. Org. Lett. 19, 2917–2920 (2017).

  25. 25.

    Zhang, B., Xiang, S.-K., Zhang, L.-H., Cui, Y. & Jiao, N. Organocatalytic asymmetric intermolecular dehydrogenative α-alkylation of aldehydes using molecular oxygen as oxidant. Org. Lett. 13, 5212–5215 (2011).

  26. 26.

    Meng, Z., Sun, S., Yuan, H., Lou, H. & Liu, L. Catalytic enantioselective oxidative cross-coupling of benzylic ethers with aldehydes. Angew. Chem. Int. Ed. 53, 543–547 (2014).

  27. 27.

    Lee, A., Betori, R. C., Crane, E. A. & Scheidt, K. A. An enantioselective cross-dehydrogenative coupling catalysis approach to substituted tetrahydropyrans. J. Am. Chem. Soc. 140, 6212–6216 (2018).

  28. 28.

    Faul, M. M. & Huff, B. E. Strategy and methodology development for the total synthesis of polyether ionophore antibiotics. Chem. Rev. 100, 2407–2474 (2000).

  29. 29.

    Kang, E. J. & Lee, E. Total synthesis of oxacyclic macrodiolide natural products. Chem. Rev. 105, 4348–4378 (2005).

  30. 30.

    Wolfe, J. P. & Hay, M. B. Recent advances in the stereoselective synthesis of tetrahydrofurans. Tetrahedron 63, 261–290 (2007).

  31. 31.

    Zhang, Z., Butt, N. A. & Zhang, W. Asymmetric hydrogenation of nonaromatic cyclic substrates. Chem. Rev. 116, 14769–14827 (2016).

  32. 32.

    Song, S., Zhu, S.-F., Pu, L.-Y. & Zhou, Q.-L. Iridium-catalyzed enantioselective hydrogenation of unsaturated heterocyclic acids. Angew. Chem. Int. Ed. 52, 6072–6075 (2013).

  33. 33.

    Kang, S. H., Lee, S. B. & Park, C. M. Catalytic enantioselective iodocyclization of γ-hydroxy-cis-alkenes. J. Am. Chem. Soc. 125, 15748–15749 (2003).

  34. 34.

    Zhou, P. et al. Catalytic asymmetric intra-and intermolecular haloetherification of enones: an efficient approach to (−)-Centrolobine. ACS Catal. 6, 7778–7783 (2016).

  35. 35.

    Bovino, M. T. et al. Enantioselective copper-catalyzed carboetherification of unactivated alkenes. Angew. Chem. Int. Ed. 53, 6383–6387 (2014).

  36. 36.

    Chung, Y. K. & Fu, G. C. Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles. Angew. Chem. Int. Ed. 48, 2225–2227 (2009).

  37. 37.

    Blanc, A. & Toste, F. D. Enantioselective synthesis of cyclic ethers through a vanadium-catalyzed resolution/oxidative cyclization. Angew. Chem. Int. Ed. 45, 2096–2099 (2006).

  38. 38.

    Tanaka, S., Seki, T. & Kitamura, M. Asymmetric dehydrative cyclization of ω-hydroxy allyl alcohols catalyzed by ruthenium complexes. Angew. Chem. Int. Ed. 48, 8948–8951 (2009).

  39. 39.

    Asano, K. & Matsubara, S. Asymmetric catalytic cycloetherification mediated by bifunctional organocatalysts. J. Am. Chem. Soc. 133, 16711–16713 (2011).

  40. 40.

    Hopkins, B. A., Garlets, Z. J. & Wolfe, J. P. Development of enantioselective palladium-catalyzed alkene carboalkoxylation reactions for the synthesis of tetrahydrofurans. Angew. Chem. Int. Ed. 54, 13390–13392 (2015).

  41. 41.

    Zheng, K. et al. Completely OH-selective FeCl3-catalyzed Prins cyclization: highly stereoselective synthesis of 4-OH-tetrahydropyrans. J. Am. Chem. Soc. 134, 17564–17573 (2012).

  42. 42.

    Tsui, G. C., Liu, L. & List, B. The organocatalytic asymmetric Prins cyclization. Angew. Chem. Int. Ed. 54, 7703–7706 (2015).

  43. 43.

    Parsons, A. T. & Johnson, J. S. Catalytic enantioselective synthesis of tetrahydrofurans: a dynamic kinetic asymmetric [3 + 2] cycloaddition of racemic cyclopropanes and aldehydes. J. Am. Chem. Soc. 131, 3122–3123 (2009).

  44. 44.

    Liu, L. et al. Catalytic asymmetric [4 + 2]-cycloaddition of dienes with aldehydes. J. Am. Chem. Soc. 139, 13656–13659 (2017).

  45. 45.

    Li, S. et al. Enantioselective hydrogenation of α-aryloxy and α-alkoxy α, β-unsaturated carboxylic acids catalyzed by chiral spiro iridium/phosphino-oxazoline complexes. J. Am. Chem. Soc. 132, 1172–1179 (2010).

  46. 46.

    Nakajima, K., Shibata, M. & Nishibayashi, Y. Copper-catalyzed enantioselective propargylic etherification of propargylic esters with alcohols. J. Am. Chem. Soc. 137, 2472–2475 (2015).

  47. 47.

    Li, Z., Yu, R. & Li, H. Iron-catalyzed C–C bond formation by direct functionalization of C–H bonds adjacent to heteroatoms. Angew. Chem. Int. Ed. 47, 7497–7500 (2008).

  48. 48.

    Reisman, S. E., Doyle, A. G. & Jacobsen, E. N. Enantioselective thiourea-catalyzed additions to oxocarbenium ions. J. Am. Chem. Soc. 130, 7198–7199 (2008).

  49. 49.

    Moquist, P. N., Kodama, T. & Schaus, S. E. Enantioselective addition of boronates to chromene acetals catalyzed by a chiral Brønsted acid/Lewis acid system. Angew. Chem. Int. Ed. 49, 7096–7100 (2010).

  50. 50.

    Maity, P., Srinivas, H. D. & Watson, M. P. Copper-catalyzed enantioselective additions to oxocarbenium ions: alkynylation of isochroman acetals. J. Am. Chem. Soc. 133, 17142–17145 (2011).

  51. 51.

    Umebayashi, N., Hamashima, Y., Hashizume, D. & Sodeoka, M. Catalytic enantioselective aldol-type reaction of β-ketosters with acetals. Angew. Chem. Int. Ed. 47, 4196–4199 (2008).

  52. 52.

    Evans, D. A. & Thomson, R. J. Ni(II) tol-BINAP-catalyzed enantioselective orthoester alkylations of N-acylthiazolidinethiones. J. Am. Chem. Soc. 127, 10506–10507 (2005).

  53. 53.

    Rueping, M., Volla, C. M. R. & Atodiresei, I. Catalytic asymmetric addition of aldehydes to oxocarbenium ions: a dual catalytic system for the synthesis of chromenes. Org. Lett. 14, 4642–4645 (2012).

  54. 54.

    Braun, M. & Kotter, W. Titanium(IV)-catalyzed dynamic kinetic asymmetric transformation of alcohols, silyl ethers, and acetals under carbon allylation. Angew. Chem. Int. Ed. 43, 514–517 (2004).

  55. 55.

    Lee, S., Kaib, P. S. J. & List, B. Asymmetric catalysis via cyclic, aliphatic oxocarbenium ions. J. Am. Chem. Soc. 139, 2156–2159 (2017).

  56. 56.

    Wang, L. et al. The important role of the byproduct triphenylphosphine oxide in the magnesium(II)-catalyzed enantioselective reaction of hemiacetals and phosphorus ylides. Angew. Chem. Int. Ed. 57, 9088–9092 (2018).

  57. 57.

    Jnoff, E. & Ghosez, L. Asymmetric Diels-Alder reactions of 2-azadienes catalyzed by a chiral copper(II) complex. A general route to enantiomerically pure piperidones. J. Am. Chem. Soc. 121, 2617–2618 (1999).

  58. 58.

    Willis, M. C., Cutting, G. A., Piccio, V. J.-D., Durbin, M. J. & John, M. P. The direct catalytic enantioselective synthesis of protected aryl β-hydroxy-α-Amino acids. Angew. Chem. Int. Ed. 44, 1543–1545 (2005).

  59. 59.

    Evans, D. A., Miller, S. J., Lectka, T. & von Matt, P. Chiral bis(oxazoline)copper (II) complexes as Lewis acid catalysts for the enantioselective Diels-Alder reaction. J. Am. Chem. Soc. 121, 7559–7573 (1999).

  60. 60.

    Evans, D. A., Downey, C. W. & Hubbs, J. L. Ni(II) bis(oxazoline)-catalyzed enantioselective syn aldol reactions of N-propionylthiazolidinethiones in the presence of silyl triflates. J. Am. Chem. Soc. 125, 8706–8707 (2003).

  61. 61.

    Poisson, T., Yamashita, Y. & Kobayashi, S. Catalytic asymmetric protonation of chiral calcium enolates via 1, 4-addition of malonates. J. Am. Chem. Soc. 132, 7890–7892 (2010).

  62. 62.

    Chen, L. et al. Bu4NI-catalyzed C–O bond formation by using a cross-dehydrogenative coupling (CDC) reaction. Chem. Eur. J. 17, 4085–4089 (2011).

  63. 63.

    Meltzer, P. C., Wang, P., Blundell, P. & Madras, B. K. Synthesis and evaluation of dopamine and serotonin transporter inhibition by oxacyclic and carbacyclic analogues of methylphenidate. J. Med. Chem. 46, 1538–1545 (2003).

  64. 64.

    Evans, D. A., Downey, C. W., Shaw, J. T. & Tedrow, J. S. Magnesium halide-catalyzed anti-Aldol reactions of chiral N-acylthiazolidinethiones. Org. Lett. 4, 1127–1130 (2002).

  65. 65.

    Fujioka, H. et al. Reaction of the acetals with TESOTf–base combination; speculation of the intermediates and efficient mixed acetal formation. J. Am. Chem. Soc. 128, 5930–5938 (2006).

  66. 66.

    Zhao, W., Li, Z. & Sun, J. A new strategy for efficient synthesis of medium and large ring lactones without high dilution or slow addition. J. Am. Chem. Soc. 135, 4680–4683 (2013).

Download references


We greatly appreciate the financial support from the National Natural Science Foundation of China (21722204, 21472112, and 21432003).

Author information


  1. School of Pharmaceutical Sciences, Shandong University, 250100, Jinan, China

    • Gang Wang
    •  & Lei Liu
  2. School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, China

    • Xiaodong Xin
    • , Zehua Wang
    • , Gang Lu
    • , Yudao Ma
    •  & Lei Liu


  1. Search for Gang Wang in:

  2. Search for Xiaodong Xin in:

  3. Search for Zehua Wang in:

  4. Search for Gang Lu in:

  5. Search for Yudao Ma in:

  6. Search for Lei Liu in:


G.W. developed the catalytic enantioselective reaction and expanded the scope. X.X. and Z.W. prepared the carboxylic acid derivatives and characterized racemic products. G.L. performed the computational experiments on the stereocontrol modeling. Y.M. discussed the results and commented on the manuscript. L.L. conceived and supervised the project, and wrote the manuscript.

Competing interests

The authors declare no competing interests.

Corresponding author

Correspondence to Lei Liu.

Supplementary Information

About this article

Publication history






By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.