Iridium-Catalyzed Arylative Cyclization of Alkynones by 1,4-Iridium Migration**

1,4-Metal migrations enable the remote functionalization of C—H bonds, and have been utilized in a wide variety of valuable synthetic methods. The vast majority of existing examples involve the 1,4-migration of palladium or rhodium. Herein, the stereoselective synthesis of complex polycycles by the iridium-catalyzed arylative cyclization of alkynones with arylboronic acids is described. To our knowledge, these reactions involve the first reported examples of 1,4-iridium migration.

Since the early reports of 1,4-palladium migration [1a-d] and 1,4-rhodium migration, [2a,b] numerous catalytic reactions involving 1,4-metal migration have been developed. [1][2][3][4][5] Such processes enable the remote functionalization of C À H bonds, allowing the introduction of metal centers at positions that would otherwise be difficult to metalate. To date, reactions involving the 1,4-migration of palladium, [1] rhodium, [2] platinum, [1q] nickel, [4] and cobalt [5] have been achieved. The demonstration of the ability of other metals to undergo 1,4migration would be valuable, as their distinct properties may offer new opportunities for the development of useful synthetic methods. Herein, we describe the preparation of highly functionalized polycycles by the iridium-catalyzed arylative cyclization of alkynones. One of the key steps in this transformation is a 1,4-iridium migration, which, to our knowledge, has not been described previously.
During a program aimed at the stereoselective synthesis of complex polycycles by the desymmetrization of cyclic 1,3diketones, [6,7] we became interested in developing an arylative cyclization of substrates such as 1 a (Scheme 1). We envisaged that in the presence of a suitable metal complex, an arylboron reagent could be employed in an arylmetalation of the alkyne moiety of 1 a to give alkenylmetal species 3. This intermediate could then undergo an alkenyl-to-aryl 1,4-migration to provide intermediate 4, which could then participate in the nucleophilic attack of one of the ketones to give tertiaryalcohol-containing tricycle 2 a. In view of the success of rhodium catalysis in related transformations, [2d-g,i,k-q] the reaction of 1 a with PhB(OH) 2 in the presence of [{Rh(cod)Cl} 2 ] (1.5 mol %), KF (1.5 equiv) as a mild base, and tBuOH (1.5 equiv) as a proton source was examined [Eq. (1)]. Heating the reaction in toluene at 65 8C for 16 hours did indeed provide tricycle 2 a in 41 % yield. However, 2 a was accompanied by the simple alkyne hydroarylation product 5 (18 % yield) and the ring-expansion product 6 (17 % yield), which is formed by initial arylation of the alkyne with the opposite regioselectivity, followed by a cyclization-fragmentation process, as described by Murakami and co-workers. [8] In an effort to increase the yield of 2 a, catalyst systems based upon other metals known to undergo 1,4-migrations (Pd, [1] Pt, [1q] Ni, [4] and Co [5] ) were surveyed. However, no reaction was observed in these experiments. Fortunately, [{Ir(cod)Cl} 2 ] (1.5 mol %) was effective, and provided 2 a in 72 % yield [Eq. (2)]. Interestingly, this experiment also gave product 7 in 27 % yield, the structure of which was determined by X-ray crystallography. [9] Compound 7 is a 2:1 adduct of 1 a and PhB(OH) 2 , respectively, resulting from a complex sequence beginning with the arylmetalation of the alkyne of 1 a with the regioselectivity opposite to that seen in the formation of 2 a. [10,11] To our knowledge, this reaction involves the first reported examples of 1,4-iridium migration. Given that the yield of 2 a was higher using an iridium-rather than a rhodium-based precatalyst, [{Ir(cod)Cl} 2 ] was selected for further studies.
The iridium-catalyzed arylative cyclization of various substrates with PhB(OH) 2 was then explored (Scheme 2). In all reactions, the 2:1 adduct was observed in approximately 10-25 % yield by 1 H NMR analysis of the reaction mixtures, but these products were not isolated. Substituents at the para, meta, or ortho positions of the aryl group on the alkyne were tolerated (2 b-f), though in the case where an ortho-cyano group was present, a higher loading of [{Ir(cod)Cl} 2 ] (2.5 mol %) was required for full conversion (2 f). With para-substituted phenyl groups, electron-poor rather than electron-rich arenes led to higher yields of the products (compare 2 b-d), which is likely due to a more regioselective initial arylmetalation of more polarized alkynes. The relative configurations of the stereogenic centers and the E geometry of the alkenes in the products were assigned by analogy with 2 d, the structure of which was determined by X-ray crystallography. [9] Substrates containing a terminal alkyne or an alkyne lacking an aryl substituent did not undergo the reaction and returned only unreacted starting material (2 g and 2 h).
Next, variations of the pendant ketone were examined. An indane-1,3-dione reacted well to give 2 i in 67 % yield. Changing the substituent at C2 (between the ketones) from a methyl to a phenyl group was tolerated, and 2 j was obtained in 63 % yield using 2.5 mol % of [{Ir(cod)Cl} 2 ]. Switching from five-to six-membered ring diketones was also possible (2 k-m [9] ). In these cases, and in a similar fashion to the fivemembered ring substrates, the reactions of substrates containing more electron-deficient arenes on the alkyne led to higher yields than those with electron-rich arenes (compare 2 k-m). A cyclic b-ketoamide was also tolerated, providing 2 n in 72 % yield.
The process is not limited to cyclic 1,3-dicarbonyl substrates in which both carbonyl groups are part of the ring; the b-ketoester 8 also underwent arylative cyclization to give 9 in 72 % yield [Eq. (3)]. However, substrate 8 was less reactive than those employed in the experiments shown in Scheme 2. Arylative cyclization of various alkynones. Reactions were conducted using 0.40 mmol of 1 a-n in toluene (4 mL). Cited yields are of isolated products. [a] Compound 7 was also isolated in 27 % yield. See Equation (2) 1, entry 6). Importantly, the reactions of metasubstituted arylboronic acids were highly regioselective (!10:1 regioisomeric ratio, determined by 1 H NMR analysis of the unpurified reaction mixtures) and provided 10 d-f as the major products (Table 1, entries 4-6). These results demonstrate that there is a strong preference for iridium to undergo 1,4-migration to the sterically least hindered site of the arene. [12] Next, the arylative cyclization of 1 a with pentadeuteriophenylboronic acid was conducted [Eq. (4)]. The product [D 5 ]-2 a was deuterated on the alkene (> 95 % deuterium incorporation by 1 H NMR analysis), a result that is consistent with the proposed mechanism involving alkenyl-to-aryl 1,4iridium migration (Scheme 1).
A possible catalytic cycle for these transformations, using 1 a and PhB(OH) 2 for illustrative purposes, is shown in Scheme 3. First, an aryliridium species 12 is generated by transmetalation from the arylboronic acid to the iridium butoxide 11 (or alternatively, an iridium fluoride). Migratory insertion of the alkyne into 12 then occurs to give alkenyliridium species 13, [13,14] which then undergoes 1,4-migration. The resulting aryliridium intermediate 14 then undergoes nucleophilic attack onto one of the ketones to give iridium alkoxide 15. Protonation of 15 with tBuOH releases the product 2 a and regenerates the iridium butoxide 11.
Preliminary attempts at developing an enantioselective variant of this process revealed that (R)-Difluorphos (L1) gave high enantioselectivities. For example, the arylative cyclization of alkynones 1 c and 1 i provided (+)-2 c and (À)-2 i in 90 % ee and 91 % ee, respectively, using 10 mol % of the iridium-bisphosphine complex under slightly modified reaction conditions compared with those used in the racemic reactions [Eqs. (5) and (6)]. [9,15] However, the activity of this iridium-bisphosphine complex was modest, and significant quantitites of the starting materials were returned. Interestingly, 2:1 adducts analogous to 7 were not observed in these reactions.