Chemo-selective cross reaction of two enals via carbene-catalyzed dual activation

A dual catalytic chemo-selective cross-coupling reaction of two enals is developed. One enal (without α-substitution) is activated by an NHC catalyst to form an acylazolium enolate intermediate that undergoes Michael-type addition to another enal molecule bearing an alkynyl substituent. Mechanistic studies indicate that non-covalent interactions between the alkynyl enal and the NHC·HX catalyst play important roles in substrate activation and enantioselectivity control. Many of the possible side reactions are not observed. Our reaction provides highly chemo- and diastereo-selective access to chiral lactones containing functionalizable 1,3-enyn units with excellent enantioselectivities (95 to >99% ee).

An NHC-catalyzed dual activation of two different enals is disclosed with both covalent and non-covalent activation pathways involved.

The development of chemo-selective reactions of two or more substrates bearing similar functional groups remains a classic challenge in organic synthesis.¹ Enals (α,β-unsaturated aldehydes) are common building blocks that offer multiple useful modes of reactions. For instance, enals are readily used as Michael acceptors in many reactions including organic catalytic reactions mediated by amines.² In the area of N-heterocyclic carbene (NHC) organocatalysis,³ enals are used as precursors of several NHC-bound intermediates, including Breslow acyl anion intermediates,⁴ homoenolate intermediates,⁵ enolate intermediates,⁶ and acylazolium intermediates.⁷ Somewhat surprisingly, on the other hand, there is little success in using enals as Michael acceptors to react with any of these NHC-bound intermediates.⁸ Elegant studies in this direction are from Scheidt, in which they showed that in the presence of an NHC catalyst, a homo coupling reaction of enals (with one enal molecule as the Michael acceptor) occurred effectively (Fig. 1a, top side).^8a,c Berkessel reported an intramolecular reaction of two enal moieties (in one molecule) to form a bicyclic lactone adduct in the presence of an achiral NHC catalyst (Fig. 1a, bottom side).^8b To the best of our knowledge, the intermolecular Michael addition reaction of two different enal substrates mediated by NHC catalysts has not been reported.⁹ Possible reasons for the difficulties of enals to behave as effective Michael acceptors likely include: (a) the relatively low electrophilicity of the α,β-unsaturated bonds of enals under the typical NHC catalytic conditions and (b) the presence of competing reactions involving both the alkene and aldehyde moieties of enals.Open in a separate windowFig. 1NHC-catalyzed reactions (a) with enals as Michael acceptors, (b) via cross intermolecular reactions of two enals, and (c) bio-active molecules bearing alkyne units.Here we disclose the first cross intermolecular reaction of two enals catalyzed by NHC catalysts (Fig. 1b). We envisioned that installation of an alkynyl substituent at the α-position of an enal can likely promote its reactivity as a Michael acceptor.¹⁰ The presence of an α-substituent can interrupt π-conjugations and thus minimize its reactivity via the corresponding enal-derived enolate/homoenolate intermediate formed with NHC, as shown by Bode, Glorius and others.^6b,11 In addition, the alkynyl substituent can promote hydrogen-bonding interactions to increase the electrophilicity of the enal to react as a Michael acceptor, as observed in Jørgensen''s amine-catalyzed reactions.¹² In our present study, a non-linear effect was observed regarding enantiomeric excesses of the NHC catalyst and the catalytic reaction product. The reaction enantioselectivity was also found to be sensitive to solvents and bases. These results suggested that the NHC and its azolium salt pre-catalyst (NHC·HX) played dual roles in our reaction: one is to activate the α-unsubstituted enal via the formation of the NHC-bound enolate intermediate,⁶ the other is to activate the α-alkynyl substituted enal via the acidic proton of the chiral NHC·HX (Fig. 1b, intermediate I & transition state TS-I).¹³ With respect to applications, carbon–carbon triple bonds are found in a good number of bioactive molecules such as cleviolide, (+)-prelaureatin, and oxamflatin (Fig. 1c).¹⁴ We demonstrated that our products containing these alkynyl units could be readily transformed into a diverse set of molecules.Cinnamaldehyde 1a and α-alkynyl enal 2a were chosen as the model substrates to search for suitable cross coupling reaction conditions (15 was used as the NHC pre-catalyst, the desired formal [4 + 2] product (3a) was obtained in a very encouraging yield (52%) with excellent ee and dr values (entry 1). The reactions appeared to be very sensitive to the structure of the NHC pre-catalysts, as similar azolium salts with N-phenyl or N–C₆F₅ substituents (B¹⁶ and C¹⁷) were completely ineffective, leading to no product formation (entries 2 & 3). Additional studies on the NHC pre-catalysts finally revealed that introduction of a Br substituent in the indane phenyl ring of the catalyst (D)¹⁸ led to 3a in 85% yield with 99% ee as nearly a single diastereomer (entry 4). Replacing Et₃N with DIEA led to similar results (entry 5). Very interestingly, when the bases were replaced with DABCO or K₃PO₄, a significant drop in the enantioselectivity was observed (entries 6 & 7; see the ESI^† for more details). Changing the solvent from THF to CHCl₃ or EtOAc has moderate effects on reaction yields (entries 8 & 9).Optimization of reaction conditions^a

Entry	NHC	Base	Solvent	Yieldb (%)	Eec (%)	Drd
1	A	Et3N	THF	52	99	>20 : 1
2	B	Et3N	THF	0	—	—
3	C	Et3N	THF	0	—	—
4	D	Et3N	THF	85	99	>20 : 1
5	D	DIEA	THF	83	98	>20 : 1
6	D	DABCO	THF	72	67	>20 : 1
7	D	K3PO4	THF	80	79	>20 : 1
8	D	Et3N	CHCl3	64	97	>20 : 1
9	D	Et3N	EtOAc	68	99	>20 : 1

Open in a separate window^aUnless otherwise specified, the reactions were carried using 1a (0.15 mmol), 2a (0.1 mmol), NHC (0.02 mmol), base (0.05 mmol) and solvent (1.0 mL) at rt for 24 h.^bIsolated yield of 3a.^cThe ee values were determined via HPLC on a chiral stationary phase.^dDr values were determined via¹H NMR of the crude reaction mixture.Our reactions are highly chemo-selective. Under all these conditions (11 Our results showed that mixing of enal 2a with highly reactive electrophiles (such as alkylidene diketone; see the ESI^† for more details) did not lead to any formal [2 + 4] addition product. Interestingly, the simple enal 1a did not behave as a Michael acceptor under our conditions, as homo-coupling adduct 3a′′ was not observed. In Scheidt''s elegant study, the introduction of a Lewis acid additive is necessary to activate one molecule of the enal to react as a Michael acceptor.^8aOur further control experiments showed that when the α-alkynl substituent of 2a was replaced with an alkyl (e.g., Fig. 2, 2a1), vinyl (2a2), phenyl (2a3) or cyano (2a4) unit, the corresponding cross [2 + 4] reactions were not observed, with most of the starting materials remaining unchanged (for more details, see the ESI^†). It is clear that the alkynl unit present in enal 2a played more important roles than simply blocking the enal α-carbon to interrupt the π-conjugations. Although attempts to identify key intermediates (and possible non-covalent interactions) between the NHC catalysts and the two enals did not lead to conclusive mechanistic pictures, our experiments did show strong non-linear effects with respect to the optical purities of the NHC pre-catalyst and the reaction product (Fig. 3, see the ESI^† for more details).Open in a separate windowFig. 2Unsuccessful α-substituted enal substrates for the NHC catalytic chemo-selective cross [2 + 4] reactions.Open in a separate windowFig. 3Nonlinear effects with respect to the product ee and the catalyst ee values using different bases: (a) Et₃N and (b) DABCO.Specifically, the reaction of 1a and 2a was studied by varying the enantiomeric purities of the NHC pre-catalyst D under the optimized reaction conditions as indicated in Fig. 3). The ee values of the products and the ee values of the catalysts showed an obvious negative nonlinear effect (Fig. 3a). This nonlinear effect suggests that at least two catalysts are involved in the enantio-differentiating step of our reaction.¹⁹ It appears both of the enals (1a and 2a) are activated by NHC and/or its salt (NHC·HX) in our formal [2 + 4] reaction. It is well established that cinnamaldehyde (1a) can be activated by NHC to form an acylazolium enolate intermediate.⁶ We therefore propose that the other enal (2a) bearing an alkynyl unit is activated by the acidic proton from NHC·HX via non-covalent interactions. These non-covalent interactions between 2a and NHC·HX could be further supported by the “linear-effect” shown by the ee values of the products and the catalysts when using DABCO as the base (Fig. 3b). In this case, only one catalyst was involved in the enantio-differentiating step of our reaction, since the non-covalent H-bonding interactions between 2a and NHC·HX could be broken by a stronger base (e.g., DABCO, K₃PO₄, see the ESI^† for details) existing in the catalytic system. Similar activation of the α-alkynyl enal by a proton was proposed in Jørgensen''s amine-catalyzed reaction.¹¹ In the field of NHC related catalysis, the use of NHC·HX as a H-bond donating catalyst has been demonstrated by Huang, Scheidt, Guin, and others.¹³The non-covalent interactions between the NHC pre-catalyst D and the alkynyl enal 2a can also be supported by ¹H NMR analysis (Fig. 4). In the presence of the weak base Et₃N, the acidic proton of the NHC pre-catalyst D shows an obvious change in the chemical shift after mixing with the alkynyl enal 2a (Fig. 4, a vs. b). Meanwhile, the chemical shift of the aldehyde proton of the substrate 2a is not changed in the same reaction system (a vs. c). These results support the existence of a non-covalent interaction between the NHC pre-catalyst D and the alkynyl enal 2a in our NHC organocatalytic reaction system (for more details, see the ESI^†).Open in a separate windowFig. 4Chemical shift of the acidic proton of the NHC pre-catalyst D under various conditions.We then examined the substrate scope using different enals (1) to react with 2a under the optimized reaction conditions indicated in Scheme 1). Substituents could be installed at each position of the phenyl ring of the cinnamaldehyde 1a, with all the products afforded in moderate to excellent yields with excellent chemo-, enantio- and diastereoselectivities (3b to 3p). The β-phenyl rings of the enal substrates (1) could also be switched to a naphthyl group or heteroaromatic groups. The corresponding products were afforded in excellent enantioselectivities, although the yields or dr values dropped in these cases (3q to 3s). To our delight, aliphatic enals could also be used as the enolate precursors for this NHC catalyzed chemoselective reaction, with the desired products afforded in moderate yields with excellent dr and ee values (3t & 3u).Open in a separate windowScheme 1Scope of enals 1. ^aReaction conditions as stated in Scheme 2). Electron-donating substituents could be well tolerated on the β-phenyl rings of the α-alkynyl enals, with the desired products afforded in good yields with excellent ee values as single diastereomers (4a & 4b). The yields of the [2 + 4] products decreased when installing electron-withdrawing groups at any position of the β-phenyl rings, although the enantioselectivities were not affected (4c to 4f). The β-phenyl rings of the α-alkynyl enal substrates (2) could also be replaced with various heteroaromatic groups without obvious reduction in the product yields or stereoselectivities (4g & 4h). Substituents were also well tolerated on the phenyl rings attached to the alkynyl units of the enal substrates 2, with all the corresponding products afforded in moderate to good yields with excellent optical purities as single diastereomers (4i to 4p). Enal substrates 2 bearing heteroaromatic, aliphatic or terminal α-alkynyl groups also worked well in this reaction and gave the target products in moderate to good yields with excellent enantio- and diastereoselectivities (4q to 4w).Open in a separate windowScheme 2Scope of α-alkynyl enals 2. ^aReaction conditions as stated in Scheme 1, 3a & Scheme 2, 4v).Having examined the reaction scope with both of the enal reactants, we next seek to get additional insights into the reaction mechanism. Hammett studies²⁰ were carried out using alkynyl enal substrates 2 bearing various p-substituents on the phenyl groups of the alkynyl units (Fig. 5). Alkynyl enal substrates 2 bearing 4-F (2i), 4-Cl (2j), 4-CF₃ (2k), 4-CH₃ (2l), and 4-OCH₃ (2m) groups were chosen as the target substrates to evaluate their relative reaction rates compared with the alkynyl enal 2a. Kinetic studies showed that the substrates 2 bearing electron-withdrawing groups reacted faster than those bearing electron-donating groups (Fig. 5a). The Hammett plot of the relative reaction rates of the substrates 2i to 2m gave a positive slope (ρ = 1.0128). Therefore, a negatively charged transition state should be built up in the rate determining step of this [2 + 4] cycloaddition process. This is in accordance with the non-covalent H-bonding interactions that we have proposed to exist between the acidic proton of the NHC-precatalyst D and the alkynyl unit of the enal substrate 2 (Fig. 1b, TS-I, see the ESI^† for more details).Open in a separate windowFig. 5(a) Kinetic data and (b) Hammet plot for the competitive [2 + 4] cycloaddition reactions based on the σ values.Additionally, substrates 2x and 2y bearing steric bulky substituted phenyl groups on the alkynyl units were further examined for this NHC dual catalytic [2 + 4] cycloaddition reaction (Fig. 6). It is not surprising that the corresponding reaction products 4x and 4y were only afforded in poor yields with moderate ee values. Because the alkynly groups of the substrates 2x and 2y were shielded by the bulky mesityl and 2,6-diisopropylphenyl groups, the H-bonding interactions between the NHC pre-catalyst D and the alkynyl groups cannot be efficiently formed in these cases.Open in a separate windowFig. 6Reactions with enals 2 bearing bulky alkynyl substituents.The chiral alkynyl pyranone products obtained from this methodology are rich in functionalities for further synthetic transformations (Fig. 7). For instance, the alkynyl group in 3a could react with the adjacent phenyl group under the catalysis of Cu(OTf)₂ to give tricyclic product 5 in a good yield without reduction of the optical purity.²¹ The terminal alkylnyl group in 4v could participate in various addition reactions and afford a variety of multi-functionalized alkene products in moderate to excellent yields with excellent ee values as single diastereomers (e.g., 6, 7, 8, 10).²² A click reaction between the alkynyl group in 4v and benzyl azide led to the formation of the chiral triazole product 9 in almost quantitative yield with excellent optical purity as a single diastereomer.^22d The ethynyl group in 4v could be selectively reduced to an ethyl group with a Pd/C and CaCO₃ catalyst in a hydrogen atmosphere (11). Pyranone 4w bearing a 2-trimethylsilylethynyl group could be coupled with 2-iodoaniline to give the indole product 12 in a moderate yield and diastereoselectivity with an excellent ee value.²³Open in a separate windowFig. 7Synthetic transformations of the chiral pyranone products. ^aCuBr₂, CH₃CN, r.t.,1 h; ^bTogni reagent, TMSCN, Cu(OAc)₂, terpyridine, CH₃CN, 70 °C, 5 h; ^cTosNHNH₂, FeCl₃, TBHP, CH₃CN, 80 °C, 8 h; ^dBnN₃, sodium l-ascorbate, DCM/H₂O (v/v = 1/1), r.t., 12 h; ^eNaI, TMSCl, H₂O, CH₃CN, r.t., 4 h; ^fPd/C, CaCO₃, H₂ (balloon), EtOH, r.t., 2 h.