Palladium-catalyzed enantioselective alkenylation of alkenylbenzene derivatives

A regioselective and enantioselective palladium-catalyzed relay Heck alkenylation of alkenylbenzene derivatives to construct remote stereocenters is disclosed.


Introduction
The migration of a metal through an alkyl chain via iterative bhydride elimination/migratory insertion processes, oen termed chain walking (or running) offers the opportunity to effectively functionalize multiple sites on a substrate. 1 Initiation of this process is oen accomplished through a metal-catalysed migratory insertion event of an alkene with applications in areas ranging from olen polymerization 2 to asymmetric catalysis. 3 Aer the initial migratory insertion and subsequent chain walking, termination events are oen coupled with either a functionalization of a metal-alkyl intermediate or reestablishing the unsaturation. 4 In this context, our lab has developed various enantioselective Heck-type reactions of di-and tri-substituted alkenes wherein the reaction is terminated by formation of a carbonyl derivative (Scheme 1A). 3,5 The formation of the aldehyde facilitates this in two key regards: (1) the penultimate proposed intermediate (C) is thermodynamically stabilized according to computational studies and (2) the resulting aldehyde does not participate in migratory insertion events thus making the process irreversible. 6 Coupled together, expanding the scope of chain walking events within a Heck platform will likely require similar tactics.
In this regard, our lab disclosed an enantioselective relay Heck arylation of alkenyl carbonyl derivatives, which delivered a,bunsaturated compounds containing remote stereocenters (Scheme 1B). 7 The a,b-unsaturated carbonyls are poor ligands compared to the initial electron rich alkene and do not participate in further Heck reactions. Combined, these results provide a basis for exploring other termination possibilities to expand the scope of these enantioselective processes. As an example, we Scheme 1 Previous work with carbonyl derivatives and proposed work with alkenylbenzene derivatives.
initially envisaged an aryl group could be employed to deliver a styrenyl product (3) or, with the addition of a transmetallating reagent, a remotely difunctionalized product (I) (Scheme 1C). From a mechanistic perspective, the Pd-alkyl intermediate (D) arising from alkene 1 and alkenyl triate 2 could undergo bhydride elimination away from the newly formed stereocenter to deliver intermediate E. We postulated that alkene E would be in equilibrium with alkene F, which would ultimately provide the thermodynamically more stable styrene product (3) aer dissociation of the Pd-hydride. However, styrene F could reinsert into the Pd-hydride bond to produce the stabilized p-benzyl intermediate (G) that could be intercepted with a transmetallating reagent to afford intermediate H followed by reductive elimination to deliver product I (in which two new stereocenters were formed). Herein, we demonstrate that the styrene product is favoured and can be produced in high enantioselectivity. Of perhaps more interest, we provide mechanistic evidence to why the reaction terminates in this fashion.

Results and discussion
To initiate our investigation, Pd 2 (dba) 3 and a pyridine oxazoline (PyrOx) ligand were combined with alkenylbenzene 1a and alkenyl triate 2a under previously reported relay Heck conditions for substrates of this type ( Table 1). 8 Under these conditions, styrenyl product 3a was isolated in 42% yield and 96 : 4 er (entry 1). The mass balance was a mixture of the undesired migratory insertion product (insertion at the alkene carbon proximal to the aryl group) and other alkene isomers 4. Switching the precatalyst to Pd(dba) 2 led to a slight increase in yield (entry 2) which was further improved to 55% with the addition of 7.5 mol% dba (entry 3). 9 Additionally, during the course of our optimization, the effect of phenylboronic acid addition was evaluated (to explore the possibility of a remote difunctionalization reaction), which resulted in an increase in the isolated yield of styrenyl product 3a (entry 4). Lastly, the addition of electron-rich para-methoxyphenylboronic acid improved the yield to 69% (entry 5). It should be noted that no remote difunctionalization product was observed with either arylboronic acid additive (entries 4 and 5); however, the yield of the styrenyl product is increased.
Aer optimized conditions were identied (entry 5), the scope of the alkenylbenzene substrate was explored ( Table 2). In general, the desired styrenyl products were obtained with moderate yields and excellent enantiomeric ratios. Again, alkenyl triate 2a was completely converted and the mass balance was mainly composed of alkene isomers 4 (a putative explanation is discussed below). A phenyl group on the substrate (1b) gave the desired styrenyl product in 64% and 96.5 : 3.5 er. A variety of electron-rich aryl groups were welltolerated including p-methyl (3c), p-methoxy (3d), o-methoxy (3e), p-hydoxy (3f), and p-dimethylamino (3g).
Additionally, electron-withdrawing substituents such as an ethyl ester (3h), two methoxy groups at the meta positions (3i), and a triuoromethyl group (3j) were all competent. A uorine atom was readily incorporated on the aromatic ring (3k-3m). Substrates containing naphthyl groups (1n and 1o) produced the desired products 3n and 3o in 57% and 44% yield, respectively. A benzodioxole group (1p) was successfully incorporated delivering styrenyl product 3p in 42% yield and 95 : 5 er. Lastly, a uoropyridyl group (1q) delivered the corresponding product (3q) in 66% yield. Trisubstituted alkene substrates were also evaluated under the reaction conditions but no desired product was observed. It should be noted that the absolute conguration of 3d was determined to be (S) and thus the rest of the products were assigned as (S) by analogy. 10 Next, the scope of alkenyl triates was investigated (Table 3). For example, 5,5-dimethylcyclohexenone triate (2r) and 2bromo-substituted triate 2s gave the corresponding products (3r and 3s) in 41% and 30% yield, respectively. An enol triate containing a methyl-substituted cyclopentenone (2t) delivered product 3t in 45% yield and 97.5 : 2.5 er. Reaction with b-keto ester derived triates 1u and 1v yielded the desired products (3u, 3v) in 52% and 60% yield, respectively. A b-keto ester derived triate containing a Boc-protected amine (1w) produced 3w in 61% yield and 98 : 2 er. Additionally, an enol triate containing a phthalimide (1x) furnished the desired styrenyl product in 51% yield and 99 : 1 er. The isolated yields of products 3u, 3v, and 3w were determined aer hydrogenation, as a mixture of alkene isomers were produced and complicated purication.
The effect of chain length on yield and selectivity was determined by comparing three additional substrates containing additional methylene units between the alkene and the aryl moiety (1y-1aa) ( Table 4). When bishomoallylic aryl compound 1y was subjected to the standard reaction conditions followed by hydrogenation, product 3y was obtained in 63% (2.6 : 1.0 ratio of insertion products). Trishomoallylic aryl compound 1z delivered product 3z in similar yield and insertion selectivity, albeit with a slightly diminished er. Lastly, when the substrate contained an additional methylene unit (1aa), product 3aa was observed in 57% yield and reduced site selectivity (2.0 : 1.0 mixture of migratory insertion products). On the basis of our previous work, 5b using (Z)-alkene substrates, the opposite enantiomer would be produced compared to reaction of the (E)-alkene. Thus, the absolute conguration of 3z and 3aa were assigned as (R). As alluded to above, interesting features of the reaction include the observation of alkene isomers using several of the differentiated aryl substrates as well as the inability to capture Pdalkyl intermediates through a subsequent cross-coupling. Therefore, we set out to interrogate the reaction mechanism with a focus on why the formation of the styrene product generally terminates the chain walking event(s). To initiate this investigation, deuterated alkenylbenzene 1y-D 2 was subjected to the optimized reaction conditions with alkenyl triate 2a ( Table  5). The goal of this study was to determine the dynamics of the chain walking process. In the event, mono-deuterated products 3y(H-D) and 3y(D-H) were observed in 23% and 12% yield, respectively. In addition, di-deuterated product 3y(D-D) was also observed in 12% yield. This mixture suggests the palladium catalyst undergoes reversible b-hydride elimination/migratory insertion at the benzylic position of the substrate, which results in the scrambling of the deuterium atoms.
To further probe the mechanism, we investigated the effect of various features of the terminating aryl group on the selective formation of styrenes. Specically, a ratio of alkene products 3 and 4 was observed as a function of the aryl group (Fig. 1A). To probe this relationship, systematic changes of the terminal aryl on this ratio were evaluated while conserving the remainder of the reaction features (Fig. 1B), and the results were compared to a number of DFT-derived physical organic parameters. These were calculated using a simple aryl model system depicted in Fig. 1C. A correlation was identied between the observed product selectivity (represented as DDG ‡ ) and the energy of an empty p* orbital as calculated by natural bond orbital (NBO) analysis (Fig. 1C). To validate this correlation, two extrapolations were tested that provide modestly improved selectivity. However, a substrate containing a para-Ph substituent performed in an unpredictable manner.
The discovery that relative p* orbital energy is correlative with the selectivity of alkene isomers formed, suggested that Pd may coordinate with the arene while chain walking. As the arene becomes less donating, the back-bonding interaction of the psystem with Pd, presumably favourable for the formation of the side product 4, is enhanced. 11 To further inspect this hypothesis, computational optimization of intermediate structures was performed. The cationic organopalladium intermediate stabilized by interactions with both the alkenyl and the terminal aryl group is calculated to be >10 kcal mol À1 lower in energy than the conformer leading up to b-hydride elimination, thus signicantly raising the energy barrier of the chain walking process (Fig. 1D). Additionally, computational results support that, through the proposed palladium-Ar bonding interaction, the g-palladium intermediates are stabilized in conformations prone to E2 elimination, with the a H-C-C-Pd dihedral angle of int-1a (4 int-1a ) being 160.8 , and 4 int-1b being 178.5 (see ESI † for further details), which through solvent mediated deprotonation will lead to minor products 4. A low-energy aryl p* orbital, which allows for strong back-bonding, can lead to both enhanced stabilizing effect, and an early transition state of the    proposed E2 elimination process. The unexpected low selectivity observed for the para-Ph-C 6 H 4 substrate can be explained by the additional non-covalent interactions of the para-position phenyl group with the ligand backbone, which further stabilizes the organopalladium intermediate for elimination. 12,5d Conclusions In summary, we have successfully developed an intermolecular enantioselective alkenylative relay Heck reaction of alkenylbenzene derivatives to synthesize enantiomerically enriched b-substituted styrenes in good to high enantioselectivity. Preliminary mechanistic studies suggest reversible b-hydride elimination/migratory insertion to arrive at the thermodynamic styrenyl product. This information will provide the foundation for the future development of new termination strategies using a metal-chain walking reaction process.

Conflicts of interest
There are no conicts to declare.