Manganese-catalyzed allylation via sequential C–H and C–C/C–Het bond activation

Manganese-catalyzed sequential C–H and C–C/C–Het bond activation to synthesize allylic alcohols, allylated arenes, functionalized cyclopentenes and skipped dienes is reported.

Complimentary to the noble hand sixth-row metals, direct C-H activation 1 using 3d-transition metal catalysis has fascinated chemists owing to their abundance, low price and low toxicity, as well as to their potential to promote novel reactivity. 2 Over the past years, the goal of achieving sustainability in organic synthesis has propelled important research in this eld and signicant progress has been made. Base-metals with exible redox ability, such as Fe, 3 Co, 4 Ni, 5 and Cu 6 are extensively used in organometallic C-H activation today. In contrast to being the third most abundant transition metal, manganese is comparatively underutilized. 7 Manganese-mediated stoichiometric C-H activation has been explored since the 1970s, however, catalytic variants of these reactions have proved challenging. 7 Recently, the groups of Kuninobu and Takai, Wang, Ackermann and others have signicantly advanced this eld of research. 8 Manganese catalysts have been found to be versatile as they can display unique reactivity and enable C-H functionalization with a variety of coupling partners containing polar multiple bonds. 8 Mechanistically, these reactions mainly involve the formal addition of a metallacycle to an unsaturated reaction partner or a substitution reaction. 8 In recent years, considerable efforts have been made to develop processes that can merge C-H activation with challenging C-C/C-Het cleavage reactions, which could allow for the efficient introduction of two different functional groups into one molecule in a single step. 9 However, most of the examples reported to date suffer from the requirement for precious transition metal catalysts and stoichiometric activators. Very recently, a manganesecatalyzed substitutive C-H allylation through highly selective C-H/C-O functionalization was achieved by Ackermann et al. 8k Owing to our continuous interest in 3d-transition metal catalysis, we questioned whether manganese catalysis can serve as an alternative route to integrating C-H activation with b-carbon/-hetero atom elimination, which is largely unexplored in this eld.
To date, cyclometalation has been the most straightforward and common method for the activation of C-H bonds. Such processes rely mainly on solvent-based techniques. From a sustainability perspective, solvent-free C-H activation processes are highly desirable. Recently, rhodium(III) and iridium(III) catalyzed C-H functionalizations under solvent-free conditions using a ball mill have been reported by  However, to the best of our knowledge, rst-row transition metal catalyzed C-H activation under neat conditions has not been developed thus far. Herein, our manganese catalyzed coupling offers an environmentally friendly, operationally simple alternative to the more traditional solvent-based protocols, featuring a cheap catalytic system. In this report, various coupling partners, including vinyl-1,3-dioxolan-2-one, 2vinyloxirane, vinylcyclopropane and diazabicycle, are applied in manganese catalysis for the rst time, leading to the convenient synthesis of allylic alcohols, allylated arenes, functionalized cyclopentenes and skipped dienes (Scheme 1).
We started our investigation by reacting N-(2-pyridyl)-indole (1a) with vinyl-1,3-dioxolan-2-one (2aa) under [Mn 2 (CO) 10 ] catalysis in diethyl ether at 80 C. This transformation involves the cleavage of a stable C-O bond to form an easily modiable C]C bond and an alcohol moiety. To our delight, the desired product 3a could be isolated in 41% yield (for details, see Table  S1 in the ESI †). Subsequently, employing [MnBr(CO) 5 ] as the catalyst precursor afforded product 3a in 84% yield in the presence of sodium acetate. The yield of 3a could be further improved to 90% by increasing the temperature to 90 C. Notably, the reaction occurred most efficiently in the absence of solvent and 3a could be isolated in 92% yield. Further experiments showed that Mn(OAc) 2 $4H 2 O or Cp*Mn(CO) 3 in lieu of [MnBr(CO) 5 ] are ineffective. Additionally, manganese is essential for this transformation as in its absence no reaction occurred.
With the optimized reaction conditions in hand, the generality of this protocol was rst tested by the reaction of indole heterocycles with 2aa and the results are given in Scheme 2. Compared to the neat conditions, our studies showed that the product 3a could be isolated in higher E/Z ratios when diethyl ether was used. Indoles substituted with reactive electrophilic functional groups which can undergo subsequent functionalization, such as the halides (-F, -Br, -I) and cyano substituents, were well tolerated. Introduction of a methyl or formyl group at the 3-position of the indole ring had no inuence on the reaction efficiency (3f-3h), indicating that the reaction tolerates steric bulk in proximity of the reaction center of 1. Moreover, this protocol was not restricted to indole substrates but also amenable to benzene-and thiophene-containing substrates, furnishing the corresponding products 3i-3k in good yields. Furthermore, an N-pyrimidyl moiety could be employed as a directing group and the expected product 3l was isolated in 79% yield. Notably, this reaction also exhibited high efficiency on a large scale. The desired product 3a could be isolated in 91% yield (1.44 g) on a 6 mmol scale. In addition, this protocol was successfully applicable to 2-vinyloxiranes, as the coupling partner, and the products 3a and 3g were isolated in 54% and 69% yield, respectively.
Encouraged by these inspiring results, we then pursued a more challenging successive C-H/C-C activation. Gratifyingly, ne tuning of the reaction conditions allowed the coupling of 1a with dimethyl 2-vinylcyclopropane-1,1-dicarboxylate (2ba) to proceed smoothly under solvent free or concentrated DMF conditions (Scheme 3). Both electron-rich (-OMe) and electron decient (-F, -Br, -I) N-(2-pyridyl)-indoles are amenable to this method, giving the corresponding products 4b-4e in 52-90% yields. A 3-methyl substituent did not diminish the reactivity, as demonstrated by the formation of the desired products 4f and 4g in excellent yields. Moreover, the scope of the arene substrate could further be extended to phenylpyridine and thiophene derivatives, affording the corresponding products 4h-4j in moderate yields.
Considering the importance of nitrogen-containing compounds and the ease of further transformation on this moiety, we next sought to apply our developed protocol to introduce a vicinal 2-arylated cyclopentenylamine unit. These are known to be key structures found within biologically active small molecules and are key intermediates in the synthesis of pharmaceutically important cyclopentane derivatives. 9e Pleasingly, when diazabicycle 2ca was utilized, the desired aryl-and amine-substituted cyclopentenes 5a-5g were obtained in 70-94% yields (Scheme 4). Not only N-(2-pyridyl)-indoles, but also Scheme 2 Unless otherwise specified, all reactions were carried out using 1 (0.2 mmol), 2 (0.3 mmol), [MnBr(CO) 5 ] (10 mol%), and NaOAc (20 mol%) in Et 2 O (1.0 mL) at 90 C under argon for 5 h, isolated yield, E/Z value given in parentheses. a Neat. b Reaction performed on a 6 mmol scale with a 47 h reaction time. c 2-Vinyloxirane (0.6 mmol) was used instead of 2aa. d 10 h. e 2-Methyl-2-vinyloxirane (0.6 mmol) was used instead of 2aa.
Olenic C-H activation could also be achieved under these conditions. For example, 2-(prop-1-en-2-yl)pyridine (1m) performed well in this transformation and the desired products 3m and 5h, a skipped diene with a valuable handle for further derivatization, were obtained in 75% and 62% yield respectively (Scheme 5).
This transformation is presumed to proceed through an organometallic C-H activation process, as was supported by radical trapping experiments (for details, see Scheme S1 in the ESI †). The reaction of 1a and 2aa under standard conditions was found to be compatible with radical scavengers 2,4-di-tert-butyl-4-methylphenol (BHT) and 1,1-diphenylethylene.
To gain more insight into the reaction mechanism, H/D scrambling experiments were next conducted (for details, see the ESI †). No H/D exchange at the 2-position of 1a was observed when 1a was simply mixed with CD 3 OD and sodium acetate. Approximately 71% deuterium was incorporated into the 2-position of recovered 1a when sodium acetate was replaced with [MnBr(CO) 5 ]. Furthermore, a larger deuterium incorporation (85%) at the 2-position of 1a was observed when 1a was treated with CD 3 OD in the presence of both [MnBr(CO) 5 ] and sodium acetate. These results suggest that the C-H activation step is reversible and might occur via a base-assisted cyclometalation process. In addition, a k H / k D ¼ 1.0 was observed from parallel reactions of 1a and [D]-1a with 2aa, respectively, which suggests that the cleavage of the C-H bond is not involved in the rate-determining step. Furthermore, when (3-pyridyl)-thiophene was utilized, the reaction occurred exclusively at the more electron rich 2position (Scheme 6). On the basis of the above-mentioned results, we may draw the conclusion that the olen coordination and insertion step is the rate-determining step, and that b-elimination is a facile process. 11 To acquire a better understanding of the observed reaction selectivity, a series of experiments were performed. As shown in Table 1, no obvious isomerization of the C]C bond was observed regardless of prolonged reaction time or decreased reaction temperature (entries 1-3, Table 1). On the contrary, solvent was found to have a dramatic effect on the E/Z selectivity (entries 3-5, Table 1). Compared to the neat reaction, DMF had a negative effect on the nal E/Z selectivity, while diethyl ether had a positive effect. From these results, we inferred that the involvement of the p-allylmanganese intermediate in the reaction mechanism might be excluded and that the solvent imparts selectivity during this transformation.
Scheme 6 Intramolecular C-H competition experiment.

Conclusions
In conclusion, we have developed a general strategy to synthesize allylic alcohols, allylated arenes, functionalized cyclopentenes and skipped dienes, in which earth abundant manganese was utilized as the catalyst. 12 This protocol represents a combination of C-H and C-C/C-Het bond activation. Both aromatic and olenic substrates are functionalized in this reaction. This work broadens the scope of manganese catalysis to include a series of new coupling partners. Additionally, this reaction can occur efficiently under neat conditions yet does not require the use of a large excess of a coupling partner as the solvent, which is unprecedented in abundant metal catalysis. Finally, b-carbon and b-nitrogen elimination were shown to be feasible under low-valent manganese catalysis for the rst time.