A copper-catalyzed double coupling enables a 3-step synthesis of the quassinoid core architecture †

The quassinoids are a fascinating class of degraded triterpene natural products which possess, among other attributes, potent anti-cancer activity. Their complex polycyclic ring systems also serve as inspiration for the development of new chemical methods and strategies – especially those pertaining to C – C bond formation. Herein we disclose a novel tandem cross coupling/S N 2 0 reaction of vicinal epoxy vinyl tri ﬂ ates with simple Grignard reagents catalyzed by Cu( I ). Using this transformation, the polycyclic core architecture of the quassinoids can be generated in only three linear steps from carvone epoxide, forming ﬁ ve carbon – carbon bonds in the process.


Introduction
Rapid generation of molecular complexity is a major driving force for 21 st century organic synthesis, and natural products continue to provide an ideal testing ground for such exploration. 1 In particular, the highly complex family of quassinoid natural products appears to be an area wherein novel methodologies could lead to great synthetic simplication. Derived from triterpenes, quassinoids are characterized by a tetracyclic ring system oen containing a D-ring lactone (see 1-4, Fig. 1A). 2 Moreover, the exciting biological proles displayed by many quassinoidsparticularly potent anti-cancer activityprovides an additional biological impetus for synthetic exploration. 3 Not surprisingly, this family of natural products have historically been popular synthetic targets and have succumbed to multiple total synthesis efforts over the past several decades. [4][5][6] We identied a hypothetical double vinylation transform of a chiral pool monoterpene as a way of accessing 5, an intermediate we envisioned advancing to the quassinoid ring system (see 6) by way of two successive ring-forming reactions (Fig. 1B). 7 Inspired by Wender's report of various organometallic reagents engaging epoxy enol ethers, enol phosphates, and enolates in S N 2 0 reactions, 8 and McMurry's seminal work on the cross coupling of vinyl triates with cuprates, 9 we envisioned developing a Cu(I)-catalyzed process to convert carvone epoxide (7) directly into functionalized cyclohexenol 9 by way of vinyl triate 8 and simple Grignard reagents (Fig. 1C). In principle, this reaction could formally introduce two sp 2 fragments in a single step and with high diastereocontrol. From the outset, however, we were aware of the paucity of Kumada-type couplings of vinyl triates and Grignard reagents catalyzed by copper, a preferred metal for S N 2 0 substitution processes. 10,11 Moreover, a mechanism by which we could distinguish between the cross-coupling and allylic substitution reactivities would be ideal in realizing the selective coupling of two different nucleophiles, but potentially challenging to implement given the similarities between the two reaction modalities. Herein we realize the one-pot double coupling of epoxy ketones with Grignard reagents catalyzed by a Cu(I) complex. Using this tandem process, we then show that the quassinoid core architecture can be accessed in only three steps, forming ve C-C bonds in the process.

Results and discussion
We began our investigations by examining the model coupling of epoxy ketone 10 with methyl Grignard to form double coupled product 12 (Table 1). We quickly realized that it was not necessary to isolate the vinyl triate intermediate (see 11) for this reaction to be successful, and in fact we encountered challenges in doing so for a variety of ketones, including 10. Much to our delight, we found that multiple copper(I) salts were competent at catalyzing this transformation, albeit with variable levels of diastereoselectivity. Most copper catalysts enforced the expected anti stereochemistry for the allylic substitution; 12 however, when the copper center was ligated with a bulky NHC ligand (entry 5), a slight preference for syn stereochemistry was observed. Of the copper sources examined, tetrakis(acetonitrile)copper(I) hex-auorophosphate [Cu(MeCN) 4 ][PF 6 ] (entry 4) seemed the most promising and was thus selected for further studies.
Diastereoselectivity could be further impacted by the inclusion of polar additives (entries [6][7][8]. HMPA (5.0 equiv.) in particular was found to bias the allylic substation to the anti isomer almost exclusively. Varying the catalyst loading (entries 9, 10) did not further impact diastereoselectivity but did have a deleterious effect on yield if the amount of catalyst was decreased below 15 mol% (5 mol% with respect to MeMgBr).
We then proceeded to explore the scope of this tandem coupling process ( Fig. 2A). Traditionally, copper catalysis has struggled to cross-couple aryl nucleophiles, due to their decreased reactivity relative to alkyl congeners. 10,11a Much to our delight, however, products derived from aromatic Grignard reagents with diverse substituents (13)(14)(15)(16)(17)(18)(19) were afforded cleanly and in good yield. 13 Other sp 2 nucleophiles relevant to the quassinoid synthetic problem including dioxenyl (20) and vinyl (21) could also be coupled, generating products as single diastereomers. Single crystal X-ray diffraction studies of 18 and 21 conrmed the anti-stereochemistry. Two substrates deserve special mention (Fig. 2B). First, 22the product formed when using the di-Grignard reagent derived from 2,2 0 -dibromobiphenylexclusively underwent cross-coupling and S N 2 opening of the epoxide, likely due to the intramolecular, and perhaps non-catalyzed, nature of the second step. Secondly, we note that 23the product of coupling allyl Grignardwas formed as a 1 : 1 mixture of syn and anti diastereomers, perhaps due to the high nucleophilicity of this reagent. 14 Different epoxide substrates were also well tolerated with this methodology (Fig. 2C). Replacement of the 2-methyl group with a larger phenyl group did not hinder product formation (see 24). Likewise, addition of a methyl group at the 3-position did not impact the reaction to prepare 25; however, that compound's tertiary allylic alcohol motif was highly acid sensitive and would rapidly dehydrate under even mildly acidic conditions. Products from both diastereomers of carvone epoxide (26, 27) were also obtained cleanly. Notably, this system was able to override the intrinsic steric bias of cis-carvone epoxide to still deliver anti product 27. Finally, we were then able to expand this methodology to perform couplings with two different nucleophiles in the same pot (Fig. 2D). We determined that at low temperatures (À78 C), the cross-coupled product could be formed selectively. This intermediate could then be treated with a different nucleophile, which would only perform the allylic substitution step when warmed to 0 C. Through this process, differentially substituted products (28-32) were assembled in a modular manner. Importantly, nucleophile identity (aryl, vinyl, alkyl, etc.) did not change the selectivity of this transformation; rather, the controlling factors in all cases were order of nucleophile addition and reaction temperature. Thus, it proved straightforward to prepare regioisomeric products 31 and 32 by simply switching which one of the nucleophiles was added rst. The connectivity and selectivity of 32 were additionally conrmed by single crystal X-ray diffraction studies.
With this methodology successfully established, we then turned our attention toward application to the quassinoid ring system (Scheme 1). We began by coupling carvone epoxide with the dioxane-based Grignard reagent to afford 33 as a single isomer in 58% yield; the anti stereochemistry of the product was conrmed by X-ray crystallographic analysis. Notably, we have been able to prepare multiple grams of this unique product using this chemistry. At this point, we reasoned that the C-and D-rings of the quassinoids could be forged through an intramolecular Diels-Alder reaction of the vinyl dioxane fragment with a dienophile side chain tethered to allylic alcohol 33. 15,16 Many initial attempts to realize this transformation were foiled due to the signicant lability of the allylic alcohol under thermal and acidic conditions. Eventually we determined that the depicted methyl chloroalkyl ether could rst alkylate the free alcohol under basic conditions (DIPEA), creating a pair of diastereomeric acetals (ca. 1 : 1 d.r.) that would then undergo the Diels-Alder reaction upon further heating. Interestingly, the acetal stereochemistry exerted a strong controlling effect on the endo/exo selectivity of the cycloaddition reaction. Specically, one acetal isomer gave exclusively the endo product (34) while the other favored exo product 35 over endo product 36 (ca. 3 : 1 exo : endo). Overall, this led to isolation of two major diastereomers, 34 and 35one endo isomer and one exo isomer (1.3 : 1 d.r.)which were used in subsequent chemistry. The stereochemistry of the exo product 35 was conrmed by single crystal X-ray diffraction studies (see ESI †). Although 34 and 35 differed in three stereocenters, they were carried forward as a mixture since we anticipated epimerization or ablation of those centers before arriving at various quassinoid natural products. 17 To complete the quassinoid core architecture, we envisioned a cascade dioxane oxidation/rearrangement/cyclization to form the A-ring. Prior work by Hanna and co-workers demonstrated that epoxidation of substituted dioxenes and rearrangement to an aldehyde occurs readily. 18 In our case, we wondered whether an acid could be identied that not only performed this rearrangement, but also promoted an intramolecular ene reaction between the newly formed aldehyde and the neighboring isopropenyl group. In practice, the desired epoxide intermediate (see bracketed intermediate, Scheme 1) was cleanly generated by treatment with DMDO and then subjected in the same pot to an assortment of Lewis acids. We found that trimethylaluminum proved to be an optimal mediator for both transformations, cleanly delivering secondary alcohols 37 and 38 in 56% combined yield. Both ene products were formed with comparable efficiency and as single isomers at the newly formed alcohol stereocenter. The stereochemistry of 38 was further conrmed by single crystal X-ray crystallographic analysis. Signicantly, the quassinoid core architecture was thus completed in only three steps from 7. Five carbon-carbon bonds and seven stereocenters were formed in the process, speaking to the power of tandem catalysis combined with synthetic strategy to assemble ornate, highly complex structures with high efficiency.

Conclusions
In summary, we have developed a novel copper-catalyzed difunctionalization reaction that converts readily available epoxy ketones to highly substituted, diastereomerically pure allylic alcohols in one pot. This transformation features a diverse substrate scope, with many classes of nucleophiles and epoxides being tolerated. Additionally, this chemistry can generate modular products by careful control of reaction conditions. The utility of this process was then demonstrated in a rapid synthesis of the quassinoid core architecture, a structure common to many bioactive natural products and one whose syntheses have historically required numerous chemical steps. Future studies are focused on employing this methodology to rapidly access high value intermediates and other complex natural product-like structures as well as synthesizing diverse quassinoid natural products.

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