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Article

Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines

by
Xiao-Lin Wang
,
Hai-Bin Jiang
,
Sheng-Cai Zheng
* and
Xiao-Ming Zhao
*
School of Chemical Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, China
*
Authors to whom correspondence should be addressed.
Molecules 2024, 29(5), 1019; https://doi.org/10.3390/molecules29051019
Submission received: 23 January 2024 / Revised: 22 February 2024 / Accepted: 23 February 2024 / Published: 26 February 2024
(This article belongs to the Special Issue Bioactive Heterocyclic Chemistry)
Browse Figures
Versions Notes

Abstract

:
A enantioselective tandem transformation, concerning asymmetric allylic decarboxylative addition and cyclization of N-nosylimines with vinylethylene carbonates (VECs), in the presence of [Rh(C2H4)2Cl]2, chiral sulfoxide-N-olefin tridentate ligand has been developed. The reaction of VECs with various substituted N-nosylimines proceeded smoothly under mild conditions, providing highly functionalized oxazolidine frameworks in good to high yields with good to excellent enantioselectivity.

1. Introduction

Rhodium-catalyzed asymmetric allylic substitution, among the efficient transition-metal catalysts, has gained increasing attention due to the development of chiral ligands in recent years [1,2,3,4,5]. Since Hayashi [6] reported the first Rh-catalyzed asymmetric allylic alkylation employing a bidentate N,P-ligand in 2003, a variety of bidentate ligands has been discovered or designed to succeed in the asymmetric allylic substitution reaction [7,8,9,10,11,12,13,14]. Recently, Li [15,16,17,18,19] developed a Rh/N,P,N-tridentate ligand [20] catalysis system, which has proven to be a powerful tool for catalyzing asymmetric allylic alkylation (AAA) reaction. A broad spectrum of nucleophiles including C, N, O, S, and even P [21] are compatible, showing a vigorousness of the tridentate ligand for allylic reaction (Scheme 1a). Very recently, we designed a tridentate sulfoxide-N-olefin hybrid Ligands and applied them in Rh-catalyzed asymmetric allylic alkylation [22] (Scheme 1b). In this study, the coordination of the olefin to rhodium is crucial to the enantioselectivity but becomes hemilabile once the catalytic cycle is finished.
Tandem reactions involving transition metal catalyzed decarboxylative addition and cyclozation of vinylethylene carbonates (VECs) are efficient ways to construct heterocycles. The key to these conversions is reckoned the in situ formation of zwitterionic π-allyl palladium intermediates during CO2 extrusion [23]. These intermediates consistently act as efficient C, O-dipoles, facilitating [3 + n] [24,25,26,27,28,29,30,31] and [5 + n] [32,33,34,35,36,37,38,39] annulation reactions for the construction of structurally diverse five- to medium-membered rings. However, Rh has rarely been reported in such enantioselective transformations despite the blooming allylic substitution reaction developed. As a continuous interest in the tridentate ligand applied in Rh-catalysis, herein we report a rhodium-catalyzed tandem asymmetric allylic decarboxylative addition and allylic substitution of vinylethylene carbonates with N-nosylimines (Scheme 1c).

2. Results and Discussion

We performed our initial study using 4-Vinyl-1,3-dioxolan-2-one 1a with N-nosylimines 2a for this reaction. In the presence of 1 mmol% of [Rh(C2H4)2Cl]2, 2 mmol% of Sulfoxide ligand L1 and Cs2CO3 in dichloromethane (DCM) at 25 °C, the expected cycloadduct 3 as diastereomers could be obtained in 32% yield with 41%/37% ee (Table 1, entry 1). And the diastereomers 3a and 3a′ can be separated through a column chromatograph.
Solvents, such as toluene, THF, MeCN and DCE (1,2-dichloroethane), were next screened (entries 2–5). This investigation led to the finding that DCE was optimal in terms of reactivity and enantioselectivity, giving the desired product 3 as in a 35% total yield, 53%/73% ee and 1.2/1 dr (entry 5 vs. entries 1–5). The base played an important role in the cycloaddition, and a series of bases including CsF, K2CO3, CsCl, Et3N, 1,8-diazabicyclo [5.4.0]-7-undecene (DBU) and N,N,N,N′-tetramethyl ethylenediamine (TMEDA) were tested (entries 5–11), CsF gave 3a/3a′ in a poor yield but with good enantioselectivity and diastereoselectivity (entry 6). Et3N was identified as the optimal base that could dramatically improve the yield and enantioselectivity (entry 9). The reaction was performed at a temperature ranging from −25 °C to 25 °C (entries 9, 12–14), and we found that the reaction at −10 °C gave superior results, giving rise to desired products in 61% yield with with good ee values (entry 13). Rhodium salts, such as Rh(acac)(C2H4)2, and [Rh(cod)Cl]2, were surveyed. Rh(acac)(C2H4)2 gave 3a/3a′ in a poor yield and low ee value (entry 15). While [Rh(cod)Cl]2 was not suitable for this reaction (entry 16).
When the catalyst loading was increased to 2 mol%, the yield and enantioselectivity of the reaction was increased (entry 17). Ligand is crucial to asymmetric allylic substitution. Therefore, structurally varying Sulfoxide ligands such as L1, L2, L3, L4, L5, and L6 were explored (Figure 1). The bidentate sulfoxide ligands L2 and L4 were less reactive, and the compounds 3a/3a′ were obtained with low yield and enantioselectivity (entry 18 and entry 20). Chirality only at sulfoxide (L3) led to decreased yield and enantioselectivity (entry 19). When the sulfoxide ligands containing imine fragments was used, the enantioselectivity dropped despite of the good yield (entry 21 and 22).
Having optimized reaction conditions in hand, the generality of the Rh-catalyzed asymmetric cycloaddition was examined using various N-nosylimines 2 (Scheme 2). The substrates 2b, 2f, 2g containing the electron-withdrawing substituent (e.g., p-Cl, m-Br and m-Cl) on the phenyl ring resulted in allyl products 3b′, 3f/3f′ and 3g/3g′ in moderate to good yields with slight decreased ee values. Products 3c′, 3d′ were all isolated in good enantioselectivity. The para phenyl substituent led to a decreased yield (3d/3d′). 1-naphthyl substituted imine was also suited for the protocol, and 3e/3e′ were garnered in a 55% total yield with 97% ee and 41% ee, respectively. Similarly, N-nosylphenylimines bearing ether substituents (–OMe, –OEt, –OPh) on the phenyl ring were well tolerated under these catalytic conditions, leading to 3h–3j in good yields (up to 61%) and enantioselectivities (up to 85% ee). In contrast, the N-nosylimines bearing a m–Me substituent showed low enantioselectivities but provided good yield in 67%. Interestingly, attaching multi-substituted groups on the phenyl ring, 3m/3m′, 3n/3n′ and 3o were also achieved in good to high yield with a high level of enantioselectivities. Heteroaryl- substrates 2p gave 3p/3p′ in an excellent yield and enantioselectivity (Scheme 2).
An X-ray diffraction analysis of the compound 3b enabled the determination of the absolute configuration of the two newly formed stereocenters [40] (Figure 2).
The scale-up synthesis of chiral oxazolidine products 3a/3a′ was conducted under the optimal conditions as shown in Scheme 3. 1a (456 mg, 4 mmol) and 2a (580 mg, 2 mmol) were employed and 3a/3a′ (440 mg, 61% yield, 85%/97% ee and 1.2/1 dr) was obtained (Scheme 3). To further demonstrate the synthetic utility of this approach, oxazolidine 3a/3a′ was successfully converted into the corresponding β-tert-β-amino alcohol under established conditions [41]. Direct hydrolysis of 3a/3a′ under acidic conditions yielded amino alcohol 4 with 81% yield and 95% ee. Subsequent protection of the alcohol with chlorotrimethylsilane in acetonitrile gave 5 (76% yield and 95% ee) [42].
Based on the previous reports [13,20], a possible mechanism was proposed. The reaction starts from the ring opening of VECs 1a by oxidative addition with a Rh(I) catalyst with the assistance of the tridentate ligand. The formed π-allyl-Rh(III) intermediate(Int-1), which already recieved 18 valance electrons and no vacant coordination for imine, could only attack the imine by oxide anion. This is a possible reason for the low diastereoselectivity. Subsequential N anion after the addition continued to proceed nucleophilic attack back to Rh(allyl) intermediate Int-2, providing allylic oxazolidines and regenerating the Rh(I) catalyst to furnish the catalytic cycle (Scheme 4).

3. Materials and Methods

3.1. Reagents and General Methods

All manipulations were carried out under the argon atmosphere using standard Schlenk techniques. All glassware were oven or flame dried immediately prior to use. All solvents were purified and dried according to standard methods prior to use, unless stated otherwise. 1H NMR spectra were obtained at 400 MHz or 600 MHz and recorded relative to the tetramethylsilane signal (0 ppm) or residual protio-solvent (7.26 ppm for CDCl3, 1.94 ppm for CD3CN). 13C NMR spectra were obtained at 100 MHz or 150 MHz, and chemical shifts were recorded relative to the solvent resonance (CDCl3, 77.16 ppm, CD3CN, 1.32 ppm). Data for NMR are recorded as follows: chemical shift (δ, ppm), multiplicity (s = singlet, d = doublet, t = triplet, m = multiplet or unresolved, br = broad singlet, coupling constant(s) in Hz, integration). Infrared spectra were recorded on Nicolet FT-IR spectrometers. The accurate masses were measured by ESI-TOF using QTOF Ultima, G2-xs TOF from Waters (Milford, MA, USA), and microflex LRF MALDI-TOF. Optical rotations αD were obtained with AUTOPOL VI from rudolph-research-analytical. HPLC using chiral stationary phase columns by comparing the samples with the appropriate racemic samples, column and elution details specified in each entry.

3.2. Synthetic Procedures

General Procedure for the Synthesis of 3 and 3′.
In a screw-cap Schlenk tube filled with argon, [Rh(C2H4)2Cl]2 (0.004 mmol, 2 mol%), Sulfoxide ligand L1 (0.008 mmol, 4 mol%), N-nosylimine 2 (0.20 mmol) were added. after that, 4-Vinyl-1,3-dioxolan-2-one 1 (0.40 mmol) and 1,2-Dichloroethane (DCE) (2.0 mL) were added. Finally, triethylamine (0.30 mmol) was added. After 24 h stirring at −10 °C, the reaction mixture was filtered over silica (CH2Cl2) and concentrated under reduced pressure to afford the crude product. The crude residue was purified by flash column chromatography (petroleum ether/ethyl acetate) to give the desired products 3 and 3′.
Representative 3 and 3′
(2R,4R)-3-((4-nitrophenyl)sulfonyl)-2-phenyl-4-vinyloxazolidine (3a): White solid; m.p.: 101–104 °C; 36% yield (26.0 mg); HPLC ee: 87% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 18.02 (major), 22.33 (minor) min]. [α]20D = +16.9 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.24 (d, J = 8.8 Hz, 2H), 7.79 (d, J = 8.8 Hz, 2H), 7.44 (d, J = 6.7 Hz, 2H), 7.38–7.32 (m, 3H), 6.21 (s, 1H), 5.76 (ddd, J = 17.9, 10.1, 8.0 Hz, 1H), 5.33 (d, J = 17.1 Hz, 1H), 5.23 (d, J = 10.2 Hz, 1H), 4.50 (q, J = 7.3 Hz, 1H), 4.10 (dd, J = 9.1, 7.0 Hz, 1H), 3.82 (dd, J = 9.1, 5.0 Hz, 1H). 13C NMR (151 MHz, CDCl3) δ 150.1, 144.7, 136.6, 135.4, 129.5, 128.9, 128.6, 127.5, 124.2, 119.3, 92.5, 71.2, 62.0. IR (CH2Cl2): νmax (cm−1) = 3055, 3005, 2972, 2875, 2304, 1715, 1530, 1347, 1274, 1262, 1171, 900, 767, 747, 735, 687. HRMS (ESI+) calcd for C17H16N2NaO5S [M + Na]+: 383.0672, Found: 383.0665.
(2S,4R)-3-((4-nitrophenyl)sulfonyl)-2-phenyl-4-vinyloxazolidine (3a′): White solid; m.p.: 101–104 °C; 29% yield (20.8 mg); HPLC ee: 98% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 17.01 (major), 20.61 (minor) min]. [α]20D = −37.3 (c 1.0, CHCl3). 1H NMR (400 MHz, CDCl3) δ 8.10 (d, J = 8.8 Hz, 2H), 7.49 (d, J = 8.8 Hz, 2H), 7.39–7.31 (m, 1H), 7.30–7.22 (m, 4H), 6.17 (s, 1H), 5.91 (ddd, J = 17.0, 10.1, 8.6 Hz, 1H), 5.42 (d, J = 17.0 Hz, 1H), 5.31 (d, J = 10.1 Hz, 1H), 4.44 (dt, J = 8.6, 5.7 Hz, 1H), 4.30 (dd, J = 8.7, 6.0 Hz, 1H), 3.86 (dd, J = 8.7, 5.4 Hz, 1H). 13C NMR (101 MHz, CDCl3) δ 149.7, 146.1, 136.7, 134.4, 129.7, 128.4, 128.3, 128.1, 123.7, 119.3, 92.4, 71.7, 62.6. IR (CH2Cl2): νmax (cm−1) = 3053, 3009, 2977, 2871, 2301, 1713, 1531, 1341, 1273, 1262, 1174, 901, 769, 750, 741, 681. HRMS (ESI+) calcd for C17H16N2NaO5S [M + Na]+: 383.0672, Found: 383.0665.
(2R,4R)-2-(4-chlorophenyl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3b): White solid; m.p.: 149–151 °C; 37% yield (29.1 mg); HPLC ee: 32% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 0.5 mL/min; detection wavelength = 214 nm; tR = 39.58 (major), 46.06 (minor) min]. [α]20D = +14.8 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.32 (d, J = 8.8 Hz, 2H), 7.89 (d, J = 8.8 Hz, 2H), 7.42 (d, J = 8.3 Hz, 2H), 7.33 (d, J = 8.3 Hz, 2H), 6.20 (s, 1H), 5.70 (ddd, J = 17.5, 10.2, 7.7 Hz, 1H), 5.31 (d, J = 17.0 Hz, 1H), 5.23 (d, J = 10.2 Hz, 1H), 4.41 (q, J = 6.8 Hz, 1H), 4.06 (dd, J = 9.1, 7.1 Hz, 1H), 3.75 (dd, J = 9.3, 5.4 Hz, 1H). 13C NMR (151 MHz, CDCl3) δ 150.4, 144.1, 135.6, 135.5, 135.0, 129.0, 128.8, 128.8, 124.4, 119.5, 91.7, 71.0, 61.9. IR (CH2Cl2): νmax (cm−1) = 3105, 3064, 2963, 2925, 2872, 2298, 1763, 1603, 1536, 1350, 1265, 1174, 1118, 856, 757, 697, 632, 576. HRMS (ESI+) calcd for C17H15ClN2NaO5S [M + Na]+: 417.0282, Found: 417.0294.
(2S,4R)-2-(4-chlorophenyl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3b′): White solid; m.p.: 149–151 °C; 25% yield (19.7 mg); HPLC ee: 83% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 0.5 mL/min; detection wavelength = 214 nm; tR = 42.76 (major), 54.28 (minor) min]. [α]20D = −22.5 (c 1.0, CHCl3).1H NMR (600 MHz, CDCl3) δ 8.19 (d, J = 8.5 Hz, 2H), 7.61 (d, J = 8.5 Hz, 2H), 7.26 (d, J = 2.2 Hz, 5H), 6.15 (s, 1H), 5.87–5.77 (m, 1H), 5.42 (d, J = 17.0 Hz, 1H), 5.30 (d, J = 10.0 Hz, 1H), 4.48–4.41 (m, 1H), 4.25 (dd, J = 8.9, 6.1 Hz, 1H), 3.84 (dd, J = 8.9, 5.2 Hz, 1H).13C NMR (151 MHz, CDCl3) δ 149.9, 146.1, 135.8, 135.5, 133.9, 129.4, 128.6, 128.6, 123.9, 119.9, 91.5, 71.6, 62.5. IR (CH2Cl2): νmax (cm−1) = 3101, 3067, 2966, 2922, 2871, 2293, 1761, 1600, 1532, 1356, 1264, 1172, 1120, 851, 754, 699, 638, 577. HRMS (ESI+) calcd for C17H15ClN2NaO5S [M + Na]+: 417.0282, Found: 417.0294.
(2R,4R)-3-((4-nitrophenyl)sulfonyl)-2-(p-tolyl)-4-vinyloxazolidine (3c): White solid; m.p.: 124–126 °C; 36% yield (26.9 mg); HPLC ee: 21% [Daicel CHIRALPAK IA-H (0.46 cm × 25 cm); n-hexane/2-propanol = 95/5; flow rate = 1.0 mL/min; detection wavelength = 254 nm; tR = 21.33 (major), 29.94 (minor) min]. [α]20D = +62.7 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.24 (d, J = 8.5 Hz, 2H), 7.79 (d, J = 8.5 Hz, 2H), 7.30 (d, J = 7.8 Hz, 2H), 7.12 (d, J = 7.8 Hz, 2H), 6.17 (s, 1H), 5.77 (ddd, J = 17.6, 10.1, 8.0 Hz, 1H), 5.33 (d, J = 17.0 Hz, 1H), 5.23 (d, J = 10.1 Hz, 1H), 4.48 (td, J = 7.4, 4.9 Hz, 1H), 4.08 (dd, J = 9.1, 7.0 Hz, 1H), 3.82 (dd, J = 9.1, 4.9 Hz, 1H), 2.35 (s, 3H). 13C NMR (151 MHz, CDCl3) δ 150.1, 144.8, 139.6, 135.5, 133.6, 129.2, 128.9, 127.5, 124.1, 119.2, 92.5, 71.1, 61.9, 21.3. IR (CH2Cl2): νmax (cm−1) = 3101, 3034, 2973, 2915, 2842, 2278, 1721, 1608, 1516, 1349, 1263, 1171, 876, 751, 687, 639. HRMS (ESI+) calcd for C18H18N2NaO5S [M + Na]+: 397.0829, Found: 397.08421.
(2S,4R)-3-((4-nitrophenyl)sulfonyl)-2-(p-tolyl)-4-vinyloxazolidine (3c′): White solid; m.p.: 124–126 °C; 24% yield (17.9 mg); HPLC ee: 85% [Daicel CHIRALPAK IA-H (0.46 cm × 25 cm); n-hexane/2-propanol = 95/5; flow rate = 1.0 mL/min; detection wavelength = 254 nm; tR = 23.94 (minor), 25.75 (major) min]. [α]20D = −20.6 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.10 (d, J = 8.8 Hz, 2H), 7.51 (d, J = 8.8 Hz, 2H), 7.14 (d, J = 7.8 Hz, 2H), 7.03 (d, J = 7.7 Hz, 2H), 6.12 (s, 1H), 5.91 (dt, J = 18.1, 9.1 Hz, 1H), 5.42 (d, J = 17.0 Hz, 1H), 5.31 (d, J = 10.1 Hz, 1H), 4.45 (dt, J = 8.5, 5.8 Hz, 1H), 4.29 (dd, J = 8.8, 6.1 Hz, 1H), 3.85 (dd, J = 8.8, 5.4 Hz, 1H), 2.35 (s, 3H). 13C NMR (151 MHz, CDCl3) δ 149.6, 146.2, 139.9, 134.5, 133.8, 128.9, 128.5, 128.1, 123.6, 119.3, 92.3, 71.7, 62.6, 21.3. IR (CH2Cl2): νmax (cm−1) = 3110, 3031, 2979, 2911, 2848, 2281, 1722, 1608, 1522, 1350, 1269, 1172, 878, 752, 688, 644. HRMS (ESI+) calcd for C18H18N2NaO5S [M + Na]+: 397.0829, Found: 397.08421.
(2R,4R)-2-([1,1′-biphenyl]-4-yl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3d): White solid; m.p.: 140–143 °C; 29% yield (25.2 mg); HPLC ee: 55% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 25.06 (major), 29.58 (minor) min]. [α]20D = +13.2 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.26 (d, J = 8.8 Hz, 2H), 7.84 (d, J = 8.8 Hz, 2H), 7.58–7.55 (m, 4H), 7.51 (d, J = 8.2 Hz, 2H), 7.46 (t, J = 7.6 Hz, 2H), 7.38 (t, J = 7.4 Hz, 1H), 6.26 (s, 1H), 5.84–5.77 (m, 1H), 5.36 (d, J = 16.9 Hz, 1H), 5.26 (d, J = 10.2 Hz, 1H), 4.50 (td, J = 7.6, 5.3 Hz, 1H), 4.12 (dd, J = 9.1, 7.0 Hz, 1H), 3.85 (dd, J = 9.2, 5.1 Hz, 1H). 13C NMR (151 MHz, CDCl3) δ 150.2, 144.6, 142.5, 140.4, 135.6, 135.4, 129.0, 128.9, 128.0, 127.8, 127.3, 127.2, 124.2, 119.4, 92.3, 71.2, 62.0. IR (CH2Cl2): νmax (cm−1) = 3109, 3064, 2993, 2911, 2815, 2235, 1712, 1635, 1509, 1356, 1234, 1163, 888, 788, 654, 616. HRMS (ESI+) calcd for C23H20N2NaO5S [M + Na]+: 459.0985, Found: 459.0990.
(2S,4R)-2-([1,1′-biphenyl]-4-yl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3d′): White solid; m.p.: 140–143 °C; 23% yield (20.0 mg); HPLC ee: 80% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 23.81 (minor), 26.79 (major) min]. [α]20D = −8.9 (c 1.0, CHCl3). 1H NMR (400 MHz, CDCl3) δ 8.11 (d, J = 8.8 Hz, 2H), 7.59–7.51 (m, 4H), 7.50–7.43 (m, 4H), 7.39 (t, J = 7.2 Hz, 1H), 7.35 (d, J = 8.2 Hz, 2H), 6.21 (s, 1H), 5.97–5.87 (m, 1H), 5.44 (d, J = 17.1 Hz, 1H), 5.33 (d, J = 10.1 Hz, 1H), 4.49 (dt, J = 8.6, 5.7 Hz, 1H), 4.33 (dd, J = 8.7, 6.1 Hz, 1H), 3.89 (dd, J = 8.8, 5.4 Hz, 1H). 13C NMR (101 MHz, CDCl3) δ 149.8, 146.2, 142.9, 140.2, 135.6, 134.4, 129.1, 128.6, 128.5, 128.0, 127.2, 127.0, 123.8, 119.4, 92.2, 71.8, 62.7. IR (CH2Cl2): νmax (cm−1) = 3109, 3060, 2999, 2910, 2819, 2232, 1721, 1633, 1505, 1353, 1234, 1161, 881, 785, 659, 610. HRMS (ESI+) calcd for C23H20N2NaO5S [M + Na]+: 459.0985, Found: 459.0990.
(2R,4R)-2-(naphthalen-1-yl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3e): White solid; m.p.: 127–129 °C; 28% yield (22.9 mg); HPLC ee: 97% [Daicel CHIRALPAK IC-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 32.07 (major), 37.52 (minor) min]. [α]20D = +28.1 (c 1.0, CHCl3). 1H NMR (400 MHz, CDCl3) δ 8.23 (t, J = 9.0 Hz, 3H), 7.93–7.79 (m, 4H), 7.67 (d, J = 7.1 Hz, 1H), 7.58–7.47 (m, 2H), 7.42 (t, J = 7.7 Hz, 1H), 6.88 (s, 1H), 6.06 (ddd, J = 17.0, 10.2, 8.1 Hz, 1H), 5.49 (d, J = 17.1 Hz, 1H), 5.40 (d, J = 10.2 Hz, 1H), 4.56 (q, J = 7.1 Hz, 1H), 4.15 (dd, J = 9.2, 7.0 Hz, 1H), 3.76 (dd, J = 9.2, 6.5 Hz, 1H). 13C NMR (101 MHz, CDCl3) δ 150.5, 143.9, 138.1, 134.8, 133.9, 132.4, 129.0, 127.6, 126.1, 125.2, 124.5, 124.0, 119.7, 91.0, 71.1, 62.0. IR (CH2Cl2): νmax (cm−1) = 3111, 3054, 2983, 2922, 2831, 2286, 1729, 1611, 1519, 1346, 1269, 1183, 877, 793, 691, 613. HRMS (ESI+) calcd for C21H18N2NaO5S [M + Na]+: 433.0829, Found: 433.0835.
(2S,4R)-2-(naphthalen-1-yl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3e′): White solid; m.p.: 127–129 °C; 27% yield (22.1 mg); HPLC ee: 41% [Daicel CHIRALPAK IC-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 214 nm; tR = 48.99 (minor), 52.06 (major) min]. [α]20D = −42.4 (c 1.0, CHCl3). 1H NMR (400 MHz, CDCl3) δ 8.06–7.99 (m, 1H), 7.95 (d, J = 8.6 Hz, 2H), 7.86 (d, J = 8.2 Hz, 1H), 7.82–7.76 (m, 1H), 7.66 (d, J = 7.1 Hz, 1H), 7.55 (d, J = 8.7 Hz, 2H), 7.48–7.41 (m, 3H), 6.75 (s, 1H), 5.99–5.84 (m, 1H), 5.52 (d, J = 17.0 Hz, 1H), 5.34 (d, J = 10.1 Hz, 1H), 4.82–4.73 (m, 1H), 4.34 (dd, J = 9.0, 6.3 Hz, 1H), 3.92 (dd, J = 9.0, 4.1 Hz, 1H). 13C NMR (101 MHz, CDCl3) δ 149.5, 145.5, 134.9, 133.9, 131.0, 130.7, 130.6, 128.8, 128.6, 127.7, 126.6, 126.0, 124.7, 123.6, 123.3, 119.5, 91.2, 71.1, 62.8. IR (CH2Cl2): νmax (cm−1) = 3108, 3052, 2988, 2929 2830, 2288, 1722, 1610, 1522, 1349, 1266, 1190, 870, 791, 694, 615. HRMS (ESI+) calcd for C21H18N2NaO5S [M + Na]+: 433.0829, Found: 433.0835.
(2R,4R)-2-(3-bromophenyl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3f): Pale yellow solid; m.p.: 117–119 °C; 34% yield (29.7 mg); HPLC ee: 81% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 254 nm; tR = 21.37 (major), 24.18(minor) min]. [α]20D = + 24.1 (c 1.0, CHCl3). 1H NMR (600 MHz, CDCl3) δ 8.31 (d, J = 8.6 Hz, 2H), 7.86 (d, J = 8.6 Hz, 2H), 7.51 (s, 1H), 7.48 (d, J = 8.0 Hz, 1H), 7.42 (d, J = 7.7 Hz, 1H), 7.24 (t, J = 7.8 Hz, 1H), 6.16 (s, 1H), 5.78–5.69 (m, 1H), 5.35 (d, J = 17.0 Hz, 1H), 5.27 (d, J = 10.2 Hz, 1H), 4.46 (q, J = 6.9 Hz, 1H), 4.14–4.07 (m, 1H), 3.78 (dd, J = 9.0, 5.4 Hz, 1H). 13C NMR (151 MHz, CDCl3) δ 150.3, 144.2, 139.1, 135.0, 132.6, 130.3, 130.2, 128.9, 126.3, 124.3, 122.7, 119.6, 91.5, 71.2, 62.0. IR (CH2Cl2): νmax (cm−1) = 3120, 3033, 2977, 2918, 2825, 2274, 1719, 1610, 1515, 1342, 1266, 1188, 870, 799, 684, 609. HRMS (ESI+) calcd for C17H15BrN2NaO5S [M + Na]+: 460.9777, Found: 460.9787.
(2S,4R)-2-(3-bromophenyl)-3-((4-nitrophenyl)sulfonyl)-4-vinyloxazolidine (3f′): Pale yellow solid; m.p.: 117–119 °C; 29% yield (25.3 mg); HPLC ee: 75% [Daicel CHIRALPAK AD-H (0.46 cm × 25 cm); n-hexane/2-propanol = 90/10; flow rate = 1.0 mL/min; detection wavelength = 254 nm; tR = 17.63 (major), 26.39 (minor) min]. [α]20D = −4.5 (c 1.0, CHCl3).1H NMR (400 MHz, CDCl3) δ 8.19 (d, J = 8.3 Hz, 2H), 7.56 (d, J = 8.4 Hz, 2H), 7.51–7.44 (m, 1H), 7.38–7.31 (m, 1H), 7.27–7.13 (m, 2H), 6.11 (s, 1H), 6.01–5.87 (m, 1H), 5.47 (d, J = 17.0 Hz, 1H), 5.36 (d, J = 10.1 Hz, 1H), 4.49 (dt, J = 9.0, 5.5 Hz, 1H), 4.31 (dd, J = 8.9, 5.7 Hz, 1H), 3.89 (dd, J = 8.9, 5.3 Hz, 1H). 13C NMR (101 MHz, CDCl3) δ 149.9, 145.9, 138.8, 134.2, 132.8, 130.8, 130.0, 128.3, 127.3, 123.9, 122.5, 119.6, 91.4, 71.8, 62.7. IR (CH2Cl2): νmax (cm−1) = 3117, 3029, 2973, 2918, 2820, 2277, 1720, 1611, 1519, 1346, 1262, 1189, 871, 7990, 682, 610. HRMS (ESI+) calcd for C17H15BrN2NaO5S [M + Na]+: 460.9777, Found: 460.9787.

4. Conclusions

In conclusion, we have utilized rhodium/tridentate sulfoxide-N-olefin hybrid Ligand catalyzed asymmetric allylic substitution to furnish a tandem reaction of VECs and various substituted N-nosylimines. Chiral oxazolidines diastereomers as (3 + 2) cycloadducts were synthesized in good to high yield, with moderate to excellent enantioselectivity. The outcome for the low diastereoselectivity is discussed, along with a proposed mechanism. More tandem reaction based on these results are undergoing in our lab.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules29051019/s1, Experimental details, NMR spectra, X-ray Crystallographic Information, HPLC Spectra, HRMS data for new products. Refs. [43,44,45,46,47] are cited in Supplementary Materials.

Author Contributions

Conceptualization, X.-M.Z.; methodology, X.-L.W. and H.-B.J.; validation, X.-L.W. and H.-B.J.; investigation, X.-L.W.; resources, X.-M.Z. and S.-C.Z.; writing—original draft preparation, X.-L.W.; writing—review and editing, X.-M.Z. and S.-C.Z.; supervision, X.-M.Z. and S.-C.Z. All authors have read and agreed to the published version of the manuscript.

Funding

National Science Foundation of China (NSFC) (grant number 21971193, 22171213) and the Fundamental Research Funds for the Central Universities.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article and Supplementary Materials.

Acknowledgments

The authors are grateful to the financial support from Tongji University.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Tsuji, J.; Minami, I.; Shimizu, I. Allyation of Carbonucleophiles with Allylic Carbonates under Neutral Conditions Catalyzed by Rhodium Complexes. Tetrahedron Lett. 1984, 25, 5157–5160. [Google Scholar] [CrossRef]
  2. Evans, P.A.; Nelson, J.D. Regioselective Rhodium-Catalyzed Allylic Alkylation with a Modified Wilkinson’s Catalyst. Tetrahedron Lett. 1998, 39, 1725–1728. [Google Scholar] [CrossRef]
  3. Evans, P.A.; Nelson, J.D. Conservation of Absolute Configuration in the Acyclic Rhodium-Catalyzed Allylic Alkylation Reaction: Evidence for an Enyl (σ + π) Organorhodium Intermediate. J. Am. Chem. Soc. 1998, 120, 5581–5582. [Google Scholar] [CrossRef]
  4. Turnbull, B.W.H.; Evans, P.A. Asymmetric Rhodium-Catalyzed Allylic Substitution Reactions: Discovery, Development and Applications to Target-Directed Synthesis. J. Org. Chem. 2018, 83, 11463–11479. [Google Scholar] [CrossRef] [PubMed]
  5. Thoke, M.B.; Kang, Q. Rhodium-Catalyzed Allylation Reactions. Synthesis 2019, 51, 2585–2631. [Google Scholar] [CrossRef]
  6. Hayashi, T.; Okada, A.; Suzuka, T.; Kawatsura, M. High Enantioselectivity in Rhodium-Catalyzed Allylic Alkylation of 1-Substituted 2-Propenyl Acetates. Org. Lett. 2003, 5, 1713–1715. [Google Scholar] [CrossRef] [PubMed]
  7. Vrieze, D.C.; Hoge, G.S.; Hoerter, P.Z.; Van Haitsma, J.T.; Samas, B.M. A Highly Enantioselective Allylic Amination Reaction Using a Commercially Available Chiral Rhodium Catalyst: Resolution of Racemic Allylic Carbonates. Org. Lett. 2009, 11, 3140–3142. [Google Scholar] [CrossRef] [PubMed]
  8. Atallah, T.; Blankespoor, R.L.; Homan, P.; Hulderman, C.; Samas, B.M.; Van Allsburg, K.; Vrieze, D.C. Substituent Effects on the Amination of Racemic Allyl Carbonates Using Commercially Available Chiral Rhodium Catalysts. Tetrahedron Lett. 2013, 54, 5795–5798. [Google Scholar] [CrossRef]
  9. Arnold, J.S.; Nguyen, H.M. Rhodium-Catalyzed Dynamic Kinetic Asymmetric Transformations of Racemic Tertiary Allylic Trichloroacetimidates with Anilines. J. Am. Chem. Soc. 2012, 134, 8380–8383. [Google Scholar] [CrossRef]
  10. Arnold, J.S.; Cizio, G.T.; Heitz, D.R.; Nguyen, H.M. Rhodium-Catalyzed Regio- and Enantioselective Amination of Racemic Secondary Allylic Trichloroacetimidates with N-Methyl Anilines. Chem. Commun. 2012, 48, 11531–11533. [Google Scholar] [CrossRef]
  11. Arnold, J.; Nguyen, H. Rhodium-Catalyzed Asymmetric Amination of Allylic Trichloroacetimidates. Synthesis 2013, 45, 2101–2108. [Google Scholar]
  12. Arnold, J.S.; Mwenda, E.T.; Nguyen, H.M. Rhodium-Catalyzed Sequential Allylic Amination and Olefin Hydroacylation Reactions: Enantioselective Synthesis of Seven-Membered Nitrogen Heterocycles. Angew. Chem. Int. Ed. 2014, 53, 3688–3692. [Google Scholar] [CrossRef]
  13. Li, C.; Breit, B. Rhodium-Catalyzed Dynamic Kinetic Asymmetric Allylation of Phenols and 2-Hydroxypyridines. Chem. Eur. J. 2016, 22, 14655–14663. [Google Scholar] [CrossRef]
  14. Tang, S.-B.; Zhang, X.; Tu, H.-F.; You, S.-L. Regio- and Enantioselective Rhodium-Catalyzed Allylic Alkylation of Racemic Allylic Alcohols with 1,3-Diketones. J. Am. Chem. Soc. 2018, 140, 7737–7742. [Google Scholar] [CrossRef]
  15. Xu, W.-B.; Ghorai, S.; Huang, W.; Li, C. Rh(I)/Bisoxazolinephosphine-Catalyzed Regio- and Enantioselective Allylic Substitutions. ACS Catal. 2020, 10, 4491–4496. [Google Scholar] [CrossRef]
  16. Li, K.; Li, C. Enantioselective Synthesis of 3-Allylindolizines via Sequential Rh-Catalyzed Asymmetric Allylation and Tschitschibabin Reaction. Org. Lett. 2020, 22, 9456–9461. [Google Scholar] [CrossRef] [PubMed]
  17. Xu, W.-B.; Sun, M.; Shu, M.; Li, C. Rhodium-Catalyzed Regio- and Enantioselective Allylic Amination of Racemic 1,2-Disubstituted Allylic Phosphates. J. Am. Chem. Soc. 2021, 143, 8255–8260. [Google Scholar] [CrossRef] [PubMed]
  18. Sun, M.; Wei, L.; Li, C. Regio- and Enantioselective Allylic Cyanomethylation by Synergistic Rhodium and Silane Catalysis. J. Am. Chem. Soc. 2023, 145, 3897–3902. [Google Scholar] [CrossRef] [PubMed]
  19. Li, B.; Luo, Y.; Liu, M.; Xia, Y.; Li, C. Asymmetric Formal Abnormal Claisen Rearrangement Enabled by Rh-Catalyzed Regio- and Enantioselective Allylic Alkylation. ACS Catal. 2023, 13, 5482–5490. [Google Scholar] [CrossRef]
  20. Jiang, Y.; Jiang, Q.; Zhu, G.; Zhang, X. Highly Effective NPN-Type Tridentate Ligands for Asymmetric Transfer Hydrogenation of Ketones. Tetrahedron Lett. 1997, 38, 215–218. [Google Scholar] [CrossRef]
  21. Li, B.; Liu, M.; Ur Rehman, S.; Li, C. Rh-Catalyzed Regio- and Enantioselective Allylic Phosphinylation. J. Am. Chem. Soc. 2022, 144, 2893–2898. [Google Scholar] [CrossRef]
  22. Zhang, M.; Chen, J.; Wang, X.; Zheng, S.-C.; Zhao, X. Tridentate Sulfoxide-N-olefin Hybrid Ligands in Rhodium-Catalyzed Asymmetric Allylic Substitution. Org. Lett. 2024, 26. Unpublished results. [Google Scholar]
  23. Liu, Z.K.; Gao, Y.; Hu, X.Q. Recent Advances in Catalytic Synthesis of Medium-Ring Lactones and their Derivatives. Catal. Sci. Technol. 2021, 11, 6931–6946. [Google Scholar] [CrossRef]
  24. Khan, A.; Yang, L.; Xu, J.; Jin, L.Y.; Zhang, Y.J. Palladium Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Michael Acceptors: Construction of Vicinal Quaternary Stereocenters. Angew. Chem. Int. Ed. 2014, 53, 11257–11260. [Google Scholar] [CrossRef] [PubMed]
  25. Khan, A.; Xing, J.X.; Zhao, J.M.; Kan, Y.H.; Zhang, W.B.; Zhang, Y.J. Palladium-Catalyzed Enantioselective Decarboxylative Cycloaddition of Vinylethylene Carbonates with Isocyanates. Chem. Eur. J. 2015, 21, 120–124. [Google Scholar] [CrossRef] [PubMed]
  26. Khan, I.; Zhao, C.; Zhang, Y.J. Pd-Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with 3-cyanochromones. Chem. Commun. 2018, 54, 4708–4711. [Google Scholar] [CrossRef] [PubMed]
  27. Liu, K.; Khan, I.; Cheng, J.; Hsueh, Y.J.; Zhang, Y.J. Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with beta-Nitroolefins by Cooperative Catalysis of Palladium Complex and Squaramide. ACS Catal. 2018, 8, 11600–11604. [Google Scholar] [CrossRef]
  28. Xia, Y.; Bao, Q.F.; Li, Y.; Wang, L.J.; Zhang, B.S.; Liu, H.C.; Liang, Y.M. Ligand-Controlled Regiodivergent Allyl Palladium Catalysis Enables a Switch between [3 + 2] and [3 + 3] Cycloadditions. Chem. Commun. 2019, 55, 4675–4678. [Google Scholar] [CrossRef] [PubMed]
  29. Xu, Y.; Chen, L.; Yang, Y.W.; Zhang, Z.; Yang, W. Vinylethylene Carbonates as α,β-Unsaturated Aldehyde Surrogates for Regioselective [3 + 3] Cycloaddition. Org. Lett. 2019, 21, 6674–6678. [Google Scholar] [CrossRef]
  30. Singha, S.; Serrano, E.; Mondal, S.; Daniliuc, C.G.; Glorius, F. Diastereodivergent Synthesis of Enantioenriched α,β-disubstituted γ-butyrolactones via Cooperative N-heterocyclic Carbene and Ir Catalysis. Nat. Catal. 2020, 3, 48–54. [Google Scholar] [CrossRef]
  31. Xiao, L.; Wei, L.; Wang, C.J. Stereodivergent Synthesis of Enantioenriched γ-Butyrolactones Bearing Two Vicinal Stereocenters Enabled by Synergistic Copper and Iridium Catalysis. Angew. Chem. Int. Ed. 2021, 60, 24930–24940. [Google Scholar] [CrossRef] [PubMed]
  32. Rong, Z.Q.; Yang, L.C.; Liu, S.; Yu, Z.; Wang, Y.N.; Tan, Z.Y.; Huang, R.Z.; Lan, Y.; Zhao, Y. Nine-Membered Benzofuran Fused Heterocycles: Enantioselective Synthesis by Pd-Catalysis and Rearrangement via Transannular Bond Formation. J. Am. Chem. Soc. 2017, 139, 15304–15307. [Google Scholar] [CrossRef] [PubMed]
  33. Yang, L.C.; Rong, Z.Q.; Wang, Y.N.; Tan, Z.Y.; Wang, M.; Zhao, Y. Construction of Nine-Membered Heterocycles through Palladium-Catalyzed Formal [5 + 4] Cycloaddition. Angew. Chem. Int. Ed. 2017, 56, 2927–2931. [Google Scholar] [CrossRef] [PubMed]
  34. Das, P.; Gondo, S.; Nagender, P.; Uno, H.; Tokunaga, E.; Shibata, N. Access to Benzo-Fused Nine-Membered Heterocyclic Alkenes with a Trifluoromethyl Carbinol Moiety via a Double Decarboxylative formal Ringexpansion Process under Palladium Catalysis. Chem. Sci. 2018, 9, 3276–3281. [Google Scholar] [CrossRef] [PubMed]
  35. Zhao, H.W.; Du, J.; Guo, J.M.; Feng, N.N.; Wang, L.R.; Ding, W.Q.; Song, X.Q. Formal [5 + 2] cycloaddition of vinylethylene carbonates to oxazol-5-(4H)-ones for the synthesis of 3,4-dihydrooxepin-2(7H)-ones. Chem. Commun. 2018, 54, 9178–9181. [Google Scholar] [CrossRef] [PubMed]
  36. Niu, B.; Wu, X.Y.; Wei, Y.; Shi, M. Palladium-Catalyzed Diastereoselective Formal [5 + 3] Cycloaddition for the Construction of Spirooxindoles Fused with an EightMembered Ring. Org. Lett. 2019, 21, 4859–4863. [Google Scholar] [CrossRef] [PubMed]
  37. Wei, Y.; Liu, S.; Li, M.M.; Li, Y.; Lan, Y.; Lu, L.Q.; Xiao, W.J. Enantioselective Trapping of Pd-Containing 1,5-Dipoles by Photogenerated Ketenes: Access to 7-Membered Lactones Bearing Chiral Quaternary Stereocenters. J. Am. Chem. Soc. 2019, 141, 133–137. [Google Scholar] [CrossRef]
  38. Zeng, R.; Li, J.L.; Zhang, X.; Liu, Y.Q.; Jia, Z.Q.; Leng, H.J.; Huang, Q.W.; Liu, Y.; Li, Q.Z. Diastereoselective Construction of 6,8-Dioxabicyclo [3.2.1]-octane Frameworks from Vinylethylene Carbonates via Palladium Organo Relay Catalysis. ACS Catal. 2019, 9, 8256–8262. [Google Scholar] [CrossRef]
  39. Wu, H.H.; Fan, X.Z.; Tang, Z.; Zhang, H.; Cai, L.Y.; Bi, X.F.; Zhao, H.W. Palladium-Catalyzed Formal (5 + 6) Cycloaddition of Vinylethylene Carbonates with Isatoic Anhydrides for the Synthesis of MediumSized N,O-Containing Heterocycles. Org. Lett. 2021, 23, 2802–2806. [Google Scholar] [CrossRef]
  40. The Cambridge Crystallographic Data Centre. CCDC 2265381. Available online: https://www.ccdc.cam.ac.uk/ (accessed on 22 February 2024).
  41. Yang, L.; Khan, A.; Zheng, R.; Jin, L.Y.; Zhang, Y.J. Pd-Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Imines. Org. Lett. 2015, 17, 6230–6233. [Google Scholar] [CrossRef]
  42. Heathcote, D.A.; Patel, H.; Kroll, S.H.B.; Hazel, P.; Periyasamy, M.; Alikian, M.; Kanneganti, S.K.; Jogalekar, A.S.; Scheiper, B.; Barbazanges, M.; et al. A Novel Pyrazolo[1,5-a]pyrimidine Is a Potent Inhibitor of Cyclin-Dependent Protein Kinases 1, 2, and 9, Which Demonstrates Antitumor Effects in Human Tumor Xenografts Following Oral Administration. J. Med. Chem. 2010, 53, 8508–8522. [Google Scholar] [CrossRef] [PubMed]
  43. Gao, N.; Guo, X.-W.; Zheng, S.-C.; Yang, W.-K.; Zhao, X.-M. Iridium-catalyzed enantioselective allylation of sodium 2-aminobenzenethiolate: An access to chiral benzo-fused N, S-heterocycles. Tetrahedron 2012, 68, 9413–9418. [Google Scholar] [CrossRef]
  44. Zhang, M.; Zhao, M.; Zheng, P.; Zhang, H.; Zhao, X. Synthesis of chiral fluorine-containing compounds via Pd-catalyzed asymmetrical allylations of dimethyl 2-fluoromalonate using sulfonamide-pyridine ligands. J. Fluorine Chem. 2016, 189, 13–21. [Google Scholar] [CrossRef]
  45. Marin, L.; Jerhaoui, S.; Kolodziej, E.; Guillot, R.; Gandon, V.; Colobert, F.; Schulz, E.; Wencel-Delord, J.; Lebœuf, D. Sulfoxide-Controlled Stereoselective Aza-Piancatelli Reaction. Adv. Synth. Catal. 2021, 363, 4277–4282. [Google Scholar] [CrossRef]
  46. Bodineau, N.; Mattali, J.-M.; Thimokhin, V.; Handoo, K.; Négrel, J.C.; Chanon, M. Formation of grignard reagents from aryl halides: Effective radical probes hint at a nonparticipation of dianions in the mechanism. Org. Lett. 2000, 2, 2303–2306. [Google Scholar] [CrossRef]
  47. Tato, F.; Reboul, V.; Metzner, P. A novel synthesis of 1-nosyl 3, 3-dichloro-β-lactams and derivatives. J. Org. Chem. 2008, 73, 7837–7840. [Google Scholar] [CrossRef]
Molecules 29 01019 sch001
Scheme 1. Background for rhodium catalyzed allylic substitution [6,7,9,13,14,15,22]. Note: The carbon with * represents a chiral center.
Scheme 1. Background for rhodium catalyzed allylic substitution [6,7,9,13,14,15,22]. Note: The carbon with * represents a chiral center.
Molecules 29 01019 sch001
Molecules 29 01019 g001
Figure 1. Ligands used in this reaction.
Figure 1. Ligands used in this reaction.
Molecules 29 01019 g001
Molecules 29 01019 sch002
Scheme 2. Scope of the allylic substrates 2 ab. a: Reaction conditions: [Rh(C2H4)2Cl]2 (0.004 mmol), L1 (0.008 mmol), 1a (0.40 mmol), 2 (0.20 mmol), Et3N (0.30 mmol), and DCE (2.0 mL). b: Yield referred to isolated yield and ee was determined by a chiral HPLC. Note: The carbon with * represents a chiral center.
Scheme 2. Scope of the allylic substrates 2 ab. a: Reaction conditions: [Rh(C2H4)2Cl]2 (0.004 mmol), L1 (0.008 mmol), 1a (0.40 mmol), 2 (0.20 mmol), Et3N (0.30 mmol), and DCE (2.0 mL). b: Yield referred to isolated yield and ee was determined by a chiral HPLC. Note: The carbon with * represents a chiral center.
Molecules 29 01019 sch002
Molecules 29 01019 g002
Figure 2. X-ray structure of 3b.
Figure 2. X-ray structure of 3b.
Molecules 29 01019 g002
Molecules 29 01019 sch003
Scheme 3. Scale-up synthesis of 3a/3a′ and the transformation for oxazolidines.
Scheme 3. Scale-up synthesis of 3a/3a′ and the transformation for oxazolidines.
Molecules 29 01019 sch003
Molecules 29 01019 sch004
Scheme 4. Possible mechanism. Note: L* represents chiral sulfoxide-N-olefin tridentate ligand.
Scheme 4. Possible mechanism. Note: L* represents chiral sulfoxide-N-olefin tridentate ligand.
Molecules 29 01019 sch004
Table 1. Optimization Study a.
Table 1. Optimization Study a.
Molecules 29 01019 i001
EntryRhLBaseSolventT (°C)Yield b (%)ee c (%)dr d
1[Rh(C2H4)2Cl]2L1Cs2CO3DCMrt3241/371.1/1
2[Rh(C2H4)2Cl]2L1Cs2CO3Tol.rt950/511.8/1
3[Rh(C2H4)2Cl]2L1Cs2CO3THFrt4712/231.1/1
4[Rh(C2H4)2Cl]2L1Cs2CO3MeCNrt2416/312/1
5[Rh(C2H4)2Cl]2L1Cs2CO3DCErt3553/731.2/1
6[Rh(C2H4)2Cl]2L1CsFDCErt2460/772/1
7[Rh(C2H4)2Cl]2L1K2CO3DCErt2931/352.2/1
8[Rh(C2H4)2Cl]2L1CsClDCErt1953/511.5/1
9[Rh(C2H4)2Cl]2L1Et3NDCErt6545/891.2/1
10[Rh(C2H4)2Cl]2L1DBUDCErt6123/252/1
11[Rh(C2H4)2Cl]2L1TMEDADCErt3965/691.4/1
12[Rh(C2H4)2Cl]2L1Et3NDCE0 6560/881.2/1
13[Rh(C2H4)2Cl]2L1Et3NDCE−10 6181/911.2/1
14[Rh(C2H4)2Cl]2L1Et3NDCE−25 5257/911.2/1
15Rh(acac)(C2H4)2L1Et3NDCE−10 4215/652/1
16[Rh(cod)Cl]2L1Et3NDCE−10 nr--
17 e[Rh(C2H4)2Cl]2L1Et3NDCE−10 6587/981.2/1
18[Rh(C2H4)2Cl]2L2Et3NDCE−10 327/52/1
19[Rh(C2H4)2Cl]2L3Et3NDCE−10 267/91.4/1
20[Rh(C2H4)2Cl]2L4Et3NDCE−10 25rac1.7/1
21[Rh(C2H4)2Cl]2L5Et3NDCE−10 5159/611.4/1
22[Rh(C2H4)2Cl]2L6Et3NDCE−10 6633/371.5/1
a Reaction conditions: Rh salt (0.001 mmol), ligand (0.002 mmol), 1a (0.20 mmol), 2a (0.10 mmol), base (0.15 mmol), and solvent (1 mL). b Isolated yield. c Determined by a chiral HPLC. d Determined by 1H NMR analysis of the crude product. e Rh salt (0.002 mmol), ligand (0.004 mmol). Note: The carbon with * represents a chiral center.
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MDPI and ACS Style

Wang, X.-L.; Jiang, H.-B.; Zheng, S.-C.; Zhao, X.-M. Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines. Molecules 2024, 29, 1019. https://doi.org/10.3390/molecules29051019

AMA Style

Wang X-L, Jiang H-B, Zheng S-C, Zhao X-M. Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines. Molecules. 2024; 29(5):1019. https://doi.org/10.3390/molecules29051019

Chicago/Turabian Style

Wang, Xiao-Lin, Hai-Bin Jiang, Sheng-Cai Zheng, and Xiao-Ming Zhao. 2024. "Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines" Molecules 29, no. 5: 1019. https://doi.org/10.3390/molecules29051019

APA Style

Wang, X. -L., Jiang, H. -B., Zheng, S. -C., & Zhao, X. -M. (2024). Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines. Molecules, 29(5), 1019. https://doi.org/10.3390/molecules29051019

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