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Organocatalytic asymmetric synthesis of oxazolines from N-acylimines
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Tengfei Xuana, 1, Yuan Pana, 1, Zhenyu Shia, Yang Wang*, a, b
Chinese Chemical Letters | 2025, 36(6) : 110352
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Chinese Chemical Letters | 2025, 36(6): 110352
• Communication •
Organocatalytic asymmetric synthesis of oxazolines from N-acylimines
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Tengfei Xuana, 1, Yuan Pana, 1, Zhenyu Shia, Yang Wang*, a, b
Affiliations
  • a Molecular Synthesis Center & Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China
  • b Laboratory for Marine Drugs and Bioproducts, Qingdao Marine Science and Technology Center, Qingdao 266237, China
Published: 2025-06-15 doi: 10.1016/j.cclet.2024.110352
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A novel organocatalytic asymmetric approach to oxazoline derivatives that proceeds through Mannich/annulation reaction of N-acylimines with 3-chlorooxindoles is presented. This strategy provides an efficient and convenient method to access enantioenriched oxazolines such as valuable chiral S, N-oxazoline ligand as well as Ferrox ligand in high yields with excellent enantio– and diastereroselectivity. Furthermore, the optically active oxazoline products can be converted to valuable 1, 2-amino alcohols. More importantly, the synthetic utility of this transformation is demonstrated in the expeditious assembly of chiral Phox-type ligand, which shows excellent catalytic activities.

Organocatalysis  /  Enantioselective  /  Oxazoline  /  N-Acylimine  /  3-Chlorooxindole
Tengfei Xuan, Yuan Pan, Zhenyu Shi, Yang Wang. Organocatalytic asymmetric synthesis of oxazolines from N-acylimines[J]. Chinese Chemical Letters, 2025 , 36 (6) : 110352 - . DOI: 10.1016/j.cclet.2024.110352
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The oxazoline structural motifs are valuable intermediates in organic transformations, glycosyl hydrolysis and polymer chemistry [1-8], and they are also prevalent scaffolds in numerous natural products and bioactive molecules [9-14]. Chiral oxazoline motifs play an important role in asymmetric synthesis, extensively serving as a preeminent class of chiral ligands (Fig. 1) [15-23]. Accordingly, the extensive use of enantioenriched oxazoline scaffolds has spawned widespread interest in the development of efficient enantioselective synthesis of optically active oxazolines, and great efforts have been devoted to this field. Based on the existing oxazole or oxazoline skeleton, chiral oxazolines can be synthesized by catalytic asymmetric hydrogenation of oxazoles [24] or alkylation of oxazolines [25-27]. In addition, catalytic asymmetric intramolecular cyclization of N-allylamides [28-39] or N-propargylamides [40], Heine reaction of N-acylaziridines [41], and desymmetrization of aminodiols [42-44] have been developed for enantioselective synthesis of oxazolines. Generally, the most common and well-established asymmetric approach to construct oxazolines is the aldol reaction of isocyanoacetates with carbonyl compounds (Scheme 1a). Since the first asymmetric aldol reaction of isocyanoacetates with aldehydes catalyzed by chiral gold(Ⅰ) catalyst was reported in 1986 by Ito and Hayashi [45], a number of transition-metal complexes, including gold [46-48], silver [49-53], palladium [54-56], platinum [57, 56, 58, 59], and cobalt [60] have been demonstrated to be effective for this aldol-type condensation. Moreover, organocatalysts [61-65] as well as the combination of transition-metal catalysis and organocatalysis [66, 67], have emerged as efficient catalyst systems in this reaction for accessing chiral oxazolines in the last decade. Recently, Denmark reported another type of intermolecular asymmetric synthesis of oxazolines from alkenes and N-tosylbenzamides (Scheme 1b) [68]. This chiral diselenide catalyzed enantioselective alkene 1, 2-oxyamination proceeded in high yields with excellent enantioselectivities. Despite these notable advancements, the development of new catalytic asymmetric intermolecular methods for the facile construction of enantiomerically pure oxazolines from a diverse array of starting materials is still highly desirable.
In sharp contrast to the abovementioned well-developed formal [3 + 2] annulation strategies, catalytic asymmetric formal [4 + 1] annulation strategy for the assembly of oxazolines is unexplored. There are some challenging issues for this [4 + 1] transformation. First is the identification of suitable four-atom starting materials that can be activated by chiral organocatalysts. Second is the identification of reactive C1 reaction partners bearing a suitable dual nucleophilic/electrophilic character that can be activated by chiral organocatalysts to undergo asymmetric [4 + 1] annulation. The final issue is the identification of effective chiral organocatalysts to control the reactivity, diastereoselectivity, and enantioselectivity of the formal [4 + 1] annulation. In this context, we envisioned that N-acylimines as four-atom reaction partners and 3-chlorooxindoles as C1 reaction partners might be suitable to access chiral oxazolines through enantioselective Mannich/annulation reaction pathway. This consideration is based on four aspects. Firstly, N-acylimines are highly reactive electrophiles. The presence of electron-withdrawing N-acyl moiety imparts to the azomethine carbon a particularly high level of electrophilicity. Secondly, because of the presence of acyl group, after the nucleophilic addition, the obtained amino intermediates are amenable in the subsequent ring closure operation. Thirdly, N-acylimines can be activated by chiral organocatalysts. Therefore, N-acylimines are particularly appreciated as suitable four-atom substrates. Fourthly, the introduction of chloro group at the C-3 position of indoles serves as an excellent leaving group in the subsequent annulation. In addition, this also increases the acidity of the C—H bond at the C-3 position of indoles. Inspired by the dual nucleophilic/electrophilic reactivity profile, it is assumed that 3-chlorooxindoles could serve as C1 reaction partners. Herein, we reported a novel and efficient organocatalytic enantioselective formal [4 + 1] annulation of N-acylimines with 3-chlorooxindoles for synthesizing a diverse range of oxazolines. The plausible transition state models that account for the bifunctional activation mode are presented in Scheme 1c. Both N-acylimine and 3-chlorooxindole are activated by the chiral organocatalyst through hydrogen-bonding interaction, which facilitates the stereoselective Mannich addition/annulation sequence, realizing the asymmetric [4 + 1] annulation.
With this design, the reaction of N-acylimine 1a with 3-chlorooxindole 2a was investigated initially as a model reaction to test the designed formal [4 + 1] annulation, with the key results summarized in Table 1. The reaction was first conducted in 1, 2-dichloroethane at 25 ℃, then DBU was used for the final annulation. Gratifyingly, in the presence of chiral cinchona alkaloid-derived thiourea organocatalyst 4a, a smooth [4 + 1] cyclization reaction indeed occurred, affording the oxazoline product 3aa in 86% yield with an excellent diastereoselectivity of > 19:1 dr, and high enantioselectivity of 91% ee (entry 1). This preliminary result demonstrated the feasibility of our hypothesis. In order to improve the enantioselectivity, a series of chiral bifunctional tertiary amine catalysts were screened (entries 2–9), and it was found that chiral cinchona alkaloid-derived squaramide catalyst 5a performed the best in enantioselectivity control (entry 5). Then, 5a was selected as the optimal catalyst to examine the solvent effect (entries 10–15). Finally, the optimal conditions were identified to be the following: 5a as catalyst and 1, 2-dichloroethane as solvent with NH4HCO3 as base at 25 ℃ for 12 h, delivering 3aa in 92% yield with excellent dr (> 19:1) and ee (98%, entry 5).
With the optimal reaction conditions in hand, large-scale reaction on 4 mmol of N-acylimine under the standard condition delivered oxazoline 3aa in 90% yield with no loss of the enantioselectivity (98% ee), demonstrating the robustness of this asymmetric [4 + 1] annulation. Consequently, a series of N-acylimines with 3-chlorooxindoles were selected to examine the tolerance of substitution patterns and functional groups in this enantioselective formal [4 + 1] annulation. This methodology was shown to be efficient for a variety of N-acylimines (Scheme 2). All of the evaluated aromatic N-acylimines bearing electron-donating and electron-withdrawing groups could provide the desired chiral oxazoline products 3ba-3ka in high yields with excellent diastereoselectivities and enantioselectivities, regardless of substitution patterns on the aromatic ring. The imines with benzo[d][1, 3]dioxol-5-yl and 2-thienyl substitution also gave good yields (86% yield for 3la, 87% for 3ma) and high enantioselectivities (97% ee for 3la, 96% ee for 3ma). It is noted that aliphatic imines failed to provide the targeted oxazolines. Various alkyl-substituted imines, such as methyl, tert–butyl and cyclohexyl were tested, however decomposition results were obtained. This might be due to the isomerization of aliphatic imines to the corresponding enamines. In addition, aliphatic imines are more unstable and susceptible to hydrolysis compared to aromatic imines. The scope of the reaction with respect to variation of acyl part of N-acylimines was then explored. Electron-rich, electron-poor and halide substitution provided access to oxazolines in excellent yields and enantioselectivities. Ortho-, meta- and para-substitution and naphthyl-substitution on the aryl ring were tolerated well (3na-3va), demonstrating good tolerance to steric crowding. Reactions of heteroatom-substituted acyl part took place smoothly, leading to the corresponding oxazolines 3wa-3c'a in high yields and excellent enantioselectivities. It is noteworthy that S, N-oxazoline ligands containing oxazoline functionality and thiophene, benzothiophene or dibenzothiophene as an auxiliary donor ligands [69, 70] could be obtained through this method. Moreover, the R2 group of N-acylimines could be ferrocenyl, furnishing chiral ferrocenyl-oxazoline 3d'a, a type of new Ferrox ligand [71, 72], in 61% yield with 94% ee.
The broad reaction scope of this formal [4 + 1] annulation was further demonstrated with different 3-chlorooxindoles (Scheme 3). The reaction tolerated broad variation in the substituent electronics of the phenyl ring on 3-chlorooxindoles, irrespective of their positions on the aromatic ring, delivering enantioenriched oxazoline products with high yields and enantioselectivities. Increasing the steric crowding and electron-withdrawing property of functional groups on the aromatic ring were not detrimental to the reaction. The reaction was also tolerant for different N-substituents on the 3-chlorooxindoles, and various N-substituted 3-chlorooxindoles were found to be amenable to the reaction conditions, giving the corresponding products 3ao-3as in excellent yields and enantioselectivities. The absolute configuration of the chiral oxazoline products was determined by the single crystal X-ray diffraction of 3aj, and those of other products were assigned accordingly.
To demonstrate the potential synthetic utilities of this enantioselective [4 + 1] annulation, various transformations of the oxazoline products were explored (Scheme 4). The derivatization of the oxazoline products was first examined through Stille cross-coupling, Suzuki cross-coupling, and Buchwald-Hartwig amination reactions with allylic stannane reagent, phenylboronic acid, and benzylamine respectively. These cross-coupling reactions proceeded well and the corresponding compounds 4–8 were obtained in high yields with maintained enantiopurity. The conversion of the oxazoline products to 1, 2-amino alcohol derivatives was conducted to further explore the synthetic potential of this reaction. Treatment of oxazoline 3aa with 1 mol/L HCl, followed by subjecting to aqueous NaHCO3 solution, delivered ring-opening 1, 2-amino alcohol 9 in 82% yield without compromising enantioselectivity. Next, the transformation of oxazoline 3aa to oxazolidine 10 was achieved smoothly without erosion of enantioselectivity through alkylation with MeOTf followed by reduction with NaBH4. Oxazolidine 10 can be converted to valuable 1, 2-amino alcohol 11 by treatment with PTSA.
Given the multitude of chiral oxazoline ligands and ever-increasing use of chiral phosphinooxazoline (Phox) ligands in catalytic asymmetric reactions, access to different novel Phox frameworks was of considerable interest and in great demand. To further showcase the synthetic versatility of our method, we anticipated that the enantioenriched oxazolines obtained in this study might provide a platform for the synthesis of novel types of chiral Phox ligand. Since the enantiopurity of 3oa could be increased up to 99% ee after recrystallization, 3oa could be converted to the corresponding Phox ligand 12 in 92% yield with 99% ee via an Ullman-type coupling (Scheme 5a). To explore the effectiveness of the obtained Phox ligand 12 in asymmetric catalysis, the preliminary application of this novel chiral Phox ligand was conducted in the allylic alkylation reaction of (E)−1, 3-diphenylallyl acetate 13 with malonate 14, affording 15 in 99% yield with 99% ee (Scheme 5b) [73, 74]. We further explored the utility of chiral Phox ligand 12 in the asymmetric allylic alkylation of allyl acetate 13 with 3-fluorooxindole 16 and found that 3, 3-disubstituted fluorooxindole 17 possessing vicinal chiral centers could be obtained in 90% yield with 96% ee [75]. Additionally, the newly designed chiral Phox ligand 12 was also successfully applied in enantioselective decarboxylative allylation of 18 to synthesize carbazolone 19, which is a valuable chiral synthetic intermediate in alkaloid synthesis. Good enantioselectivity consistent with literature report was achieved [76]. These preliminary explorations demonstrated that the chiral Phox ligand 12 had promising potential as a new class of oxazoline ligand.
Next, to provide some experimental support for the proposed transition states, we tried to isolate the key intermediate of this reaction. The reaction of N-acylimine 1a with 3-chlorooxindole 2a catalyzed by chiral catalyst 5a under ammonium bicarbonate in DCE at 25 ℃ was performed, and an uncyclized intermediate 20 was isolated in 95% yield with 98% ee (Scheme 6). Treatment of this key intermediate 20 with DBU at 80 ℃ could give the final cyclized oxazoline product 3aa in 97% yield with 98% ee. Therefore, this reaction was a stepwise [4 + 1] annulation, and the enantiocontrol and diastereocontrol of this reaction was achieved in Mannich addition.
In conclusion, we have developed a novel organocatalytic asymmetric approach to oxazoline derivatives that proceeds through Mannich/annulation reaction of N-acylimines with 3-chlorooxindoles. This strategy provides an efficient and convenient method to access enantioenriched oxazolines especially valuable chiral S, N-oxazoline ligand as well as Ferrox ligand in high yields with excellent enantio– and diastereroselectivity. Furthermore, the reaction shows a broad substrates scope and can be applied to the expeditious assembly of valuable chiral 1, 2-amino alcohols as well as chiral oxazoline-type ligand such as chiral Phox ligand owning excellent catalytic activities, demonstrating the utility of this strategy.
Declaration of competing interest
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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
CRediT authorship contribution statement
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Tengfei Xuan: Methodology, Data curation. Yuan Pan: Methodology, Data curation. Zhenyu Shi: Data curation. Yang Wang: Writing – review & editing, Writing – original draft, Supervision, Project administration.
Acknowledgments
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We thank Qingdao Marine Science and Technology Center (No. 2022QNLM030003–2), the Fundamental Research Funds for the Central Universities, Taishan Scholar Program of Shandong Province (No. tsqn202103152), National Natural Science Foundation of China (No. 22201270), Natural Science Foundation of Shandong Province (No. ZR2021QB033), the National Key Research and Development Program of China (No. 2022YFC2804400) for financial support.
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2024.110352.
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Year 2025 volume 36 Issue 6
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Article Info
doi: 10.1016/j.cclet.2024.110352
  • Receive Date：2024-03-18
  • Online Date：2025-10-29
  • Published：2025-06-15
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  • Received：2024-03-18
  • Revised：2024-08-12
  • Accepted：2024-08-21
Affiliations
    a Molecular Synthesis Center & Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China
    b Laboratory for Marine Drugs and Bioproducts, Qingdao Marine Science and Technology Center, Qingdao 266237, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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