Abstract
Herein, we report a copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides and 1,3-enynes, which provides a series of chiral poly-substituted pyrrolidines in high regio-, diastereo-, and enantioselectivities. Both 4-aryl-1,3-enynes and 4-silyl-1,3-enynes serve as suitable dipolarophiles while 4-alkyl-1,3-enynes are inert. Moreover, the method is successfully applied in the construction of both tetrasubstituted stereogenic carbon centers and chiral spiro pyrrolidines. The DFT calculations are also conducted, which imply a concerted mechanism rather than a stepwise mechanism. Finally, various transformations started from the pyrrolidine bearing a triethylsilylethynyl group and centered on the alkyne group are achieved, which compensates for the inertness of 4-alkyl-1,3-enynes in the present reaction.
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Introduction
Chiral poly-substituted pyrrolidines are not only key structure units in both natural and man-made bioactive molecules but also versatile intermediates in organic synthesis1,2,3,4,5,6,7,8,9,10. One of the most efficient methods to access these compounds is the transition metal-catalyzed asymmetric 1,3-dipolar cycloaddition11,12,13,14,15,16,17,18. Among various metal catalysts, copper(I) catalysts have gained a prominent position, which exhibited admiring abilities to enable high reaction efficiency and wonderful asymmetric induction19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34. Various 1,3-dipoles, such as nitrones, azomethine ylides, and azomethine imines, serve as wonderful substrates. The dipolarophiles are generally limited to strongly activated alkenes, including α,β-unsaturated compounds and α,β,γ,δ-unsaturated compounds35 (Fig. 1a). The strong electron-withdrawing groups include aldehyde, ketone, ester, amide, cyano, nitro, sulfone, and phosphonate. However, catalytic asymmetric 1,3-dipolar cycloadditions with weakly activated alkenes are very uncommon and thus remain elusive36,37,38,39,40,41.
In 2016, Cossío, Adrio, and Carretero reported a copper(I)- or silver(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides and weakly activated alkenes (Fig. 1b, left). In this reaction, vinylarenes bearing electron-deficient aryl groups, as well as vinylheteroarenes, were used as satisfactory 1,3-dipoles36. In 2021, Chung, Wang, and co-workers successfully developed a copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of β-substituted alkenyl heteroarenes by using a powerful chiral monodentate phosphoramidite ligand (Fig. 1b, right)38. Other notable examples are copper-catalyzed asymmetric 1,3-dipolar cycloadditions of fullerenes and cyclopropenes with azomethine ylides39,40,41,42,43. The highly strained nature of the olefin unit in fullerenes enabled the reaction. Despite these leading achievements, the scope of weakly activated alkenes is still significantly limited. Moreover, it is noted that the products in these reactions are structurally specific, which does not allow facile further transformations based on the electron-deficient aryls or heteroaryls. Thus research efforts on the reaction with weakly activated alkenes that are easily functionalized at a later stage are highly desirable11,12,13,14,15,16,17,18.
1,3-Enynes were initially used as important intermediates in the synthesis of highly substituted aromatic rings44,45. Then Krische pioneered the transition metal-catalyzed three-component coupling reactions with 1,3-enynes46,47,48,49,50,51,52,53,54,55. In 2004, Krische and co-workers uncovered a rhodium-catalyzed reductive coupling of 1,3-enynes and α-keto aldehydes under a hydrogenation atmosphere, which afforded (E)-2-hydroxy-3,5-dien-1-one products46. In 2008, the same group disclosed a ruthenium-catalyzed reductive coupling of 1,3-enynes and alcohols, providing synthetically versatile homopropargyl alcohols52. These instructive works stimulated further extensive investigations on the utilization of 1,3-enynes in three-component coupling reactions and other interesting transformations56,57,58, especially copper-catalyzed asymmetric syntheses of propargyl alcohols/amines59,60,61,62,63 and allenes64,65,66,67,68,69,70,71,72,73. Based on these seminar reports, it is envisioned that the presence of a conjugated carbon-carbon triple bond may lead to weak activation of the olefin group and thus may lower the LUMO energy (Fig. 1c). Thus, 1,3-enynes may serve as potential efficient dipolarophiles. Moreover, the presence of a carbon-carbon triple bond would allow further facile functionalization of the pyrrolidines produced via 1,3-dipolar cycloadditions.
Herein, we would like to disclose a copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides and 1,3-enynes. A series of chiral poly-substituted pyrrolidines were prepared in moderate to high yields with moderate to high diastereo- and enantioselectivities. Remarkably, 1,4-disubstituted 1,3-enynes also served as a suitable dipolarophile. Furthermore, the present methodology worked efficiently in the construction of both tetrasubstituted stereogenic carbon centers and chiral spiro pyrrolidines. The chemical calculations indicated that a concerted reaction pathway rather than a step-wise one was more reasonable for the present reaction. Moreover, the activation ability of the terminal olefin by several substituents was studied, which gave us a clear understanding of the reactivities of these weakly activated terminal olefins. At last, multiple transformations showcased the synthetic versatility of the triethylsilylethynyl group and thus complemented the substrate shortage of 4-alkyl-1,3-enynes.
Results and discussion
Initially, the reaction between iminoester 1a and 1,3-enyne 2a was investigated for the optimization of reaction conditions (Fig. 2). In the presence of 5 mol% Cu(CH3CN)4PF6, 6 mol% (R)-Tol-BINAP, and 20 mol% KOtBu, 3aa was produced in 44% yield with 10/1 dr and 29% ee (entry 1). Several bisphosphines and (R,RP)-tBu-FOXAP were screened (entries 2–7), which identified (R)-DTBM-SEGPHOS as the best in terms of yield, dr, and ee (entry 7, 72% yield, >20/1 dr, 80% ee). Switching the solvent from THF to toluene led to increased enantioselectivity but with decreased both yield and dr (entry 8, 45% yield, 16/1 dr, 97% ee). DCM was found to be the most suitable solvent as 3aa was obtained in 72% yield with >20/1 dr and 98% ee (entry 9). Barton’s base worked with similar efficiency (entry 10). However, weaker organic bases, such as Et3N and Cy2NMe, were found to be ineffective. The reaction with Cs2CO3 as the base afforded 3aa in excellent yield together with excellent diastereo- and enantioselectivities (entry 11, 96% yield, >20/1 dr, 98% ee). The yield was further enhanced in DCE by increasing the substrate concentration from 0.1 to 0.4 M (entry 12, 99% yield, >20/1 dr, 98% ee). The reaction results of both tbutyl and benzyl esters (1a′ and 1a′′) were also satisfactory (entry 13, 99% yield, >20/1 dr, 96% ee; entry 14, 98% yield, >20/1 dr, 98% ee). It should be noted that only one type of regioisomers was observed in these reactions.
Under the optimum reaction conditions, the substrate scope of iminoester (1) was studied with 2a as the dipolarophile (Fig. 3). The reaction results were not very sensitive to both the substitution pattern and the electronic nature of the aryl groups as the corresponding products were isolated in generally high yields with excellent diastereo- and enantioselectivities (3ba–3ja, 72–99%, 14/1–20/1 dr, 95–98% ee). However, moderate dr (14/1) was observed in the case of 3ca and moderate yield (72%) was obtained in the reaction of 3ia. Moreover, 1-naphthyl and 2-naphthyl were well accepted (3ka–3la, 95–96%, >20/1 dr, 94% ee). Heteroaryl substituents were also well tolerated, and the corresponding products were obtained with excellent results (3ma–3oa, 94–98%, >20/1 dr, 91–97% ee). As for the aliphatic iminoesters (1p–1s), (S,SP)-tBu-FOXAP was found as a better ligand than (R)-DTBM-SEGPHOS. Under higher substrate concentration (1.0 M), several aliphatic iminoesters reacted with 2a smoothly to provide the corresponding products in acceptable results (3pa–3sa and 3ri, 57–73%, 9/1–12/1 dr, 79–90% ee). However, the results of aliphatic iminoesters were inferior to the results of aromatic ones. The absolute configuration of 3ri was determined by X-ray analysis of its derivative’s single crystals (for the details, see SI), which led to the assignment of the configurations of 3pa–3sa.
Then the substrate scope of 1,3-enynes (2) was investigated with 1a as the 1,3-dipole precursor (Fig. 4). At first, 1,3-enynes bearing a terminal olefin were evaluated (R′ = H). The R group could be various aromatic substituents (3ab–3am, 80–99%, 13/1–20/1 dr, 93–99% ee). Clearly, both the substitution pattern and the electronic nature of the aryl groups did not have a significant effect on yield, diastereo-, or enantioselectivities. However, the electron-donating group led to slightly decreased both yield and diastereoselectivity (3ad, 80%, 13/1 dr). Heteroaromatic substituents were well accepted in the R group (3an–3ao, 78–97%, >20/1 dr, 98–99% ee). When the R group was an aliphatic substituent (such as PhCH2CH2-), the reaction did not proceed at all. Fortunately, the R group could be either an additional alkynyl group or an N-Bn-sulfamide, and the products were isolated with satisfying results (3ap–3aq, 80–96%, >20/1 dr, 98–99% ee). Furthermore, 1,3-enyne 2r containing a triethylsilyl group served as a satisfactory 1,3-dipolarophile, which was transformed to 3ar in 80% yield with >20/1 dr and 99% ee. Evidently, the synthetically versatile triethylsilylethynyl group allows facile late-stage functionalization. Then trans-1,4-disubsituted 1,3-enyne 2s (R = Ph, R′ = Me) was tried in the present reaction. Although the yield was moderate in the reaction with 10 mol% copper(I) catalyst and 40 mol% Cs2CO3, both the diastereo-, and enantioselectivities were very high (3as, 49%, >20/1 dr, 92% ee). Interestingly, cis-1,3-enyne 2t (R = Ph, R′ = Me) exhibited similar performances in the present catalytic system (3at, 54%, >20/1 dr, 98% ee). It should be noted that 3as and 3at are diastereoisomers. The absolute configuration of 3ai was determined unambiguously by X-ray crystal diffraction. The stereochemistry of other products (3aa–3oa and 3ab–3at) was deduced by structural analogy. It should be pointed out that the relative configuration of 3as was further confirmed by the X-ray analysis of its single crystals.
Subsequently, the present method was applied in the construction of tetrasubstituted stereocenters (Fig. 5). By introducing a methyl group at the α-position in the iminoester, substrate 4 was obtained for this purpose. The reactions of 4 and several 1,3-enynes proceeded nicely with excellent diastereo- and high enantioselectivities (6a, 6d, 6j, 6n, and 6r, >20/1 dr, 78–92% ee). However, yields varied considerably (28–99%). At 60 °C, as low as 28% yield was obtained for 6d, and 58% yield was observed for 6n. Undoubtedly, the yield increased significantly with the decrease in the electronic density of the 1,3-enynes. The method was further applied in the synthesis of chiral spiro compounds. Remarkably, four chiral spiro pyrrolidines were prepared in uniformly high yields and high enantioselectivity (7a, 7d, 7i, and 7r, 80–94%, 89–93% ee). However, the diastereoselectivity was moderate (6/1–14/1 dr). The absolute configuration of 7i was established by X-ray crystallographic analysis of its single crystals. The stereochemistry of other products (6 and 7) was assigned analogically.
With the present copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition as a tool, several olefins, including but-3-en-1-yn-1-ylbenzene (2a), but-3-en-1-yn-1-yltriethylsilane (2r), (E)-buta-1,3-dien-1-ylbenzene (8), hex-5-en-3-yn-1-ylbenzene (2u), and styrene (9), were evaluated. As shown in Fig. 6, 2a exhibited the highest reactivity, possibly due to the double activation of the olefin by both the conjugated alkyne and the conjugated phenyl groups. 2r displayed the second-highest reactivity as both the conjugated alkyne group and the triethylsilyl group activated the olefin. Clearly, the phenyl group had a stronger activation effect on the conjugated terminal olefin than the triethylsilyl group. The reaction with 8 was very slow and led to a low yield (12%), indicating that the activation effect of the conjugated alkene group on the terminal olefin is much weaker than the conjugated alkyne group. Such an experimental fact could be rationalized by the realization that two π-bonds are present in the alkyne while only one π-bond is present in the alkene, which leads to superior activation of the terminal olefin in 2a to the one in 8. 2u and 9 remained intact, suggesting that the activation of the olefin singly by the alkyne or the phenyl is not enough for the present 1,3-dipolar cycloaddition.
In literature36, it was proposed that the copper(I)-catalyzed 1,3-dipolar cycloaddition of strongly activated olefins prefers a stepwise mechanism while the reaction of weakly activated olefins prefers a concerted mechanism. Thus it is believed that the present reaction proceeds preferentially in a concerted mechanism. To elucidate the mechanistic details, DFT calculations were performed by employing iminoester 1a, 1,3-enyne 2a, ligand (R)-DTBM-SEGPHOS, and Cu(CH3CN)4PF6 as depicted in Fig. 7. The computational results showed that the present reaction proceeded preferentially in a concerted mechanism rather than the stepwise mechanism (for details, see SI). Based on the concerted mechanism, the stereoselectivity-determining cyclization step was revealed, and the relative free energies of the enantio-isomeric transition states and their structures were obtained, which are depicted in Fig. 7. TS1 (leading to the desired product 3aa) is more favorable by 2.6 kcal mol−1 than TS2 (leading to ent-3aa). Evidently, the calculation results are in good agreement with the experimental enantioselectivity (98% ee), which validates the calculated concerted reaction pathway. Through analysis of the structures of the competing transition states TS1 and TS2, the close distance between one of the tBu groups in (R)-DTBM-SEGPHOS and the alkynyl and phenyl groups in 1,3-enyne 2a in the disfavored TS2 leads to more van der Waals interactions (for details, see SI) and bigger dihedral angle of C88–C85–C64–C63 in the relatively unfavored cyclization transition state, which results in the observed absolute stereochemistry.
At last, transformations were performed with 3ar as a model substrate (Fig. 8). The catalytic hydrogenation of 3ar at room temperature provided silane 10 in 87% yield. The deprotection of 3ar afforded terminal alkyne 11 in 94% yield. The Sonogashira coupling of 11 with vinylbromide furnished 1,3-enyne 12 in 91% yield. Notably, the coupling proceeded smoothly in the presence of a free secondary amine moiety. Moreover, the click reaction of 11 and benzyl azide occurred nicely to deliver triazole 13 in 71% yield. The protection of the secondary amine moiety underwent easily gave terminal alkyne 14, which was ready for the CuI-catalyzed cross-coupling reaction between terminal alkyne and allyl bromide74. 1,4-Enyne 15 was synthesized in 90% yield. The hydroboration of the terminal olefin75 in 15 was readily performed to offer boronate 16 in 60% yield. It should be mentioned that further transformations based on silane, 1,3-enyne, terminal alkyne, terminal olefin, and boronate were straightforward. Moreover, some of the above transformations compensated for the inertness of 4-alkyl-1,3-enynes in the present 1,3-dipolar cycloaddition.
Methods
General procedures for copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of 1,3-enynes: a dried 25 ml schlenk tube equipped with a magnetic stirring bar was charged with [Cu(MeCN)4]PF6 (3.7 mg, 0.01 mmol, 0.05 equiv), Cs2CO3 (13.0 mg, 0.04 mmol, 0.2 equiv), and (R)-DTBM-SEGPHOS (14.0 mg, 0.012 mmol, 0.06 equiv) in a glove box under Ar atmosphere. Anhydrous DCE (0.5 ml) was added via a syringe. The mixture was stirred for 30 min at room temperature. Then imine esters (0.26 mmol, 1.3 equiv) and 1,3-enynes (0.2 mmol, 1.0 equiv) were added sequentially. The resulting mixture was stirred at room temperature for 12 or 18 h. Then the reaction mixture was directly purified by silica gel column chromatography to give the desired product.
Data availability
All data are available from the authors upon request. Supplementary information and chemical compound information are available along with the online version of the paper. The X-ray crystallographic coordinates for structures reported in this study have been deposited at the Cambridge Crystallographic Data Center (CCDC) under deposition numbers 2093924, 2111662, 2106096, and 2111496. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. Cartesian coordinates of the optimized structures are provided in a supplementary data file.
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Acknowledgements
We gratefully acknowledge the financial support from the National Natural Science Foundation of China (Nos. 21871287, 21922114, and 22271302), the Science and Technology Commission of Shanghai Municipality (Nos. 20JC1417100, 21XD1424800, and 20400750300), the Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine (ZYYCXTD-202004), CAS Key Laboratory of Synthetic Chemistry of Natural Substances, and Shanghai Institute of Organic Chemistry. We are also grateful to Professor Xin Hong and Professor Xiao-Song Xue for their help and advices on the chemical calculations. Moreover, Mr. Jia-Wei Jiang is acknowledged for the check on the reproducibility of this work.
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L.Y., P.T., and D.D.G. conceived and designed the study. B.R.W., Y.B.L., and Q.Z. performed the synthetic experiments and analyzed data for all new compounds. Q.H.L. did the chemical calculation work. L.Y. and P.T. wrote the paper.
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Wang, BR., Li, YB., Zhang, Q. et al. Copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of 1,3-enynes and azomethine ylides. Nat Commun 14, 4688 (2023). https://doi.org/10.1038/s41467-023-40409-4
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DOI: https://doi.org/10.1038/s41467-023-40409-4
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