Ketones as directing groups in photocatalytic sp3 C–H fluorination† †Electronic supplementary information (ESI) available. CCDC 1556373, 1556374 and 1556555. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc02703f

Visible light-sensitization allows conformationally rigid ketones to act as “directing groups” for aliphatic fluorination using Selectfluor, catalytic benzil, and LEDs.

Innate selectivity in aliphatic C-H bond uorination is achieved when most other C-H bonds are either sterically hindered or electronically deactivated. These factors allow very little control and versatility with respect to radical uorination of intricate substrates, especially at sites near electron-withdrawing groups such as ketones. Consider the uorination of 2-dodecanone ( Fig. 1). Using existing methods, the reaction will result in a complicated mixture of uorinated isomers with the relative product ratio increasing the farther the site is from the ketonea well-documented manifestation of the "polar effect". 1 What if the desired site of uorination is in proximity to the carbonyl (beyond the a-position accessible through enolate chemistry 2 )? Under the right conditions, it is possible that the role of a ketone can be switched from a deactivator to an activator (i.e. directing group) on rigid molecular skeletons where the ketone oxygen atom is properly poised. 3 Herein, we report the ability of ketones to function as directing groups under visible lightsensitized uorination conditions, thus allowing greater control over regioselectivity in radical-based uorination.
Considering the prominent role of uorine in medicinal chemistry, 4 surprisingly few directed sp 3 C-H uorination reactions have been developed beyond extant benzylic 5 or allylic uorination methods. 6 Several aliphatic uorination methods have been reported recently using transition metal catalysts, 7 radical initiators, 8 organic molecule catalysts, 9 and photosensitizers, 10 but these methods generally are geared toward small, symmetrical molecules or those with more activated or accessible C-H bonds. With respect to more biologically relevant molecules, selective b-uorination of amino acid derivatives has been achieved through palladium catalysis using a chelating auxiliary ligand in a three-step ligand installation-uorinationligand removal process. [11][12][13] In our laboratory, we have recently developed an enone-directed photochemical uorination of polycyclic terpenoid derivatives through direct 300 nm photolysis. 14 Unfortunately, under the same reaction conditions (using ultraviolet light), we found that ketones afford highly unselective uorination and are not optimal directing groups; thus, a different approach was necessary.
We imagined that a milder procedure that employs visible light sensitization could allow the necessary balance between reactivity and selectivity to bring the more general and important concept of a ketone-directed reaction to fruition (Fig. 2).  Accordingly, we report a visible light-sensitized ketone-directed C-H uorination method using catalytic benzil (10 mol%), Selectuor (as a putative atomic source of uorine 15 ), and cool white LED's. 16 Under these mild conditions, predictably selective bor g-uorination can be achieved based on proximity of the hydrogen atom to the ketone. Both cyclic and exocyclic ketones are demonstrated to direct uorination effectively on a variety of mono-, di-, tri-, and tetracyclic systems (such as steroidal ketones) in up to 85% yield. In accord with most excited-state ketone hydrogen atom transfer (HAT) chemistry, we found that structural rigidity plays an important role in attaining both desired reactivity and selectivity. 17 However, we report initial ndings that an electron transfer mechanism (either concerted PCET or stepwise ET/PT) is more likely operative.
In order to establish an optimal photosensitizer, we began by screening a variety of compounds with a steroidal ketone test substrate (1) poised for g-hydrogen atom transfer, Selectuor, and a cool white LED source. Note that the LED source, with a sharp absorbance cut-off at ca. 400 nm by UV-vis analysis (see ESI †), was used instead of a compact uorescent light (CFL) source, as the latter has a minor absorbance in the ultraviolet region. Accordingly, we focused primarily on putative sensitizers that possess absorbances above 400 nm; this measure was taken to avoid undesirable reactivity from direct excitation of the substrate and/or uorine source (corroborated by control experiments that show no reaction in the absence of a sensitizer or light). Although a number of compounds effected the uorination reaction to form 2 (Table 1), we found the overall best results (82% yield) using a catalytic amount of benzila wellestablished triplet sensitizer that is commercially available, extremely cost-effective, and easy to handle. 18, 19 It is important to note that the use of other N-F reagents as putative sources of atomic uorine, i.e. NFSI and N-uoropyridinium tetrauoroborate, do not result in the desired uorinated product 2. Although NFSI can also react with alkyl radicals, Selectuor has been shown to react at a faster rate and may be more likely to participate in electron transfer processes (discussed below). 15a,24 Additionally, no uorination reaction was observed upon stirring all three components in the dark at room temperature or running the photochemical reaction under ambient air. Heating the reaction mixture to reux in the dark also did not afford 2, but trace unidentied tertiary uorides were observed in the 19 F NMR spectrum of the crude reaction mixture. Finally, a slight decrease in product yield was observed when using Selectuor in greater than 1.5 equiv. (Table 1, entry 6); this is a function of a decrease in selectivity, as greater quantities of other uorinated isomers were observed by 19 F NMR analysis of the crude reaction mixture.
With an optimized protocol in hand, we focused our efforts on evaluation of the substrate scope with respect to a variety of common ring systems ( Table 2). Menthone contains two tertiary carbon sites, but we observe strictly compound 3 in 55% yield under uorination conditions, consistent with the notion of ketone involvement (note that although a putative 6-membered transition state from one of the methyl groups can be imagined, we did not observe primary uorides). Compounds 4 and 5 represent examples of benzylic uorination through putative 5membered transition states. It is important to note that ethylbenzene does not undergo benzylic uorination under the same conditions, suggesting the ketone plays a necessary role. In addition, compound 4 demonstrates reaction compatibility with a boron-based functional group (pinacolborane) that is used widely in cross-coupling applications. 20 In these instances, the tertiary and benzylic C-H sites are arguably more activated toward uorination. Thus, we examined substrates that should target specic secondary carbon Benzil 73 a 7 Benzil 82 a Reaction with 2.0 equiv. Selectuor. sites. Employing an exocyclic ketone on a rigid norbornane scaffold, we were able to access a mixture of exo and endo uorides (6) at the predicted site in 70% yield. Beyond bridged bicyclic systems, there are also opportunities for ketonedirected uorination on certain decalone cores. For instance, compound 7 (derived from sesquiterpenoid valencene) was formed selectively in the presence of other tertiary carbon sites distal from the ketone. Subsequently, we examined directed uorination on more complex tricyclic ring systems. For one, a longifolene-derived ketone provided selective uorination of the most accessible carbon site on the cycloheptane ring (8). Remarkably, we were also able to target a C-H bond on a strained cyclobutane ring to form uorinated kobusone derivative 9. What is more, this reaction proceeded smoothly in the presence of an oxidized sulfur-containing functional group (i.e. a tosylate).
Considering the prevalence and importance of biologically active steroidal ketones, 21 we surveyed the uorination of ketones akin to cholesterol derivative 2 (Table 3). Compounds 10-12 represent cholesterol, testosterone, and progesterone derivatives with starting ketones at C7 also poised for C15 functionalization. Note that compound 10 also exhibits reaction tolerance of aliphatic chlorides. Selective g-uorination was observed in each case (62-85% yield).
Subsequently, we applied the ketone-directed reaction to b-uorination on the steroid core. Thus, a C6 steroidal ketone was found to uorinate the C4 position through a putative 5membered transition state to afford 13 in 65% yield. No evidence of degradation to the corresponding enone was observed following column chromatography on silica gel. In another instance, C12-uorinated trans-androsterone derivative 14 (with an expanded D-ring) was also readily accessible. Recognizing that uorinated trans-androsterone derivatives may be more desirable with the cyclopentane ring intact, we asked: will the cyclopentanone also access C12 uorination through a 5-membered transition state? To our satisfaction, compound 15 was formed in 59% yield. We also examined a tricyclic secosteroid substrate (16) as another example of a cyclopentanone moiety directing uorination to the adjacent cyclohexane ring.
Importantly, note that the virtue of the tetra-and tricyclic ring systems discussed thus far is their decreased conformational exibility; this allows for selective, predictable uorination in a somewhat paradoxical manner. That is, more complex polycyclic carbon frameworks, in general, promote selective C-H uorination where it intuitively may inhibit it in other nondirected circumstances. Thus, this method appears to be best suited for late-stage uorination of larger, more intricate structures. 22 On another note, the ideal substrates for this reaction have a clear distinction over the preference for gvs. b-uorination based on geometric constraints. However, how does the reaction proceed when both 5-and 6-membered transition states are possible? Progesterone, with an acetyl group at C17, can act as a probe and also provide a real-world example of when this competitive uorination could be of interest (i.e. to access different uorinated bioactive steroids). Accordingly, we found that the free rotation of the s-bond between C17 and C20 allows uorination of both C12 (17) and C16 (18) in a ratio of 1.0 : 3.1 (55% total yield, Scheme 1). Although the regioselectivity is modest, this may be an asset in a medicinal chemistry setting where multiple uorinated regioisomers of similar steroids are desirable for biological testing. 23 Table 3 Substrate scope: steroidal ketone directing groups for predictable g-or b-fluorination of sp 3 C-H sites a a Unless otherwise specied, all reactions were stirred in MeCN with Selectuor (1.5 equiv.) and benzil (10 mol%) and irradiated with cool white LED's for 14 h. Yields include both diastereomers and were determined by integration of 19 F NMR signals relative to an internal standard and conrmed by isolation of products through column chromatography on silica gel. Major diastereomer (with respect to C-F bond) depicted where known.
At this point, we have demonstrated cyclic (5-and 6-membered rings) and exocyclic aliphatic ketones directing uorination on either cyclic (4-, 5-, 6-, and 7-membered rings) or short, linear side-chain sites. How does the reaction hold up to linear aliphatic ketones? Using 2-heptanone as the substrate, we observed d-, g-, and b-uorination in 2.3 : 1.3 : 1.0, respectively, in the 19 F NMR spectrum of the crude reaction mixture. This could indicate an indiscriminate radical chain mechanism instead of a directed reaction, 24,25 as it exhibits features of the so-called polar effect. 1 In order to expand on this result, we also ran the reaction with 2-decanone and 2-dodecanone. In each case, there was a large preference for uorination at the penultimate carbon atom alongside multiple secondary uoride isomers (Fig. 1).
Thus, under the same reaction conditions, the rigid ketones afford selective bor g-uorination and the conformationally exible ketones do not. Perhaps the linear ketones (1) prefer intermolecular over intramolecular HAT and/or (2) promote cage escape of the N-centered radical derived from Selectuor that is a key player in radical chain mechanisms. 24,25 Accordingly, we ran the reactions with the linear ketones under more dilute conditions to favor intramolecular HAT, 26 but observed the same product distributions by 19 F NMR. What is more, a HAT mechanism directed by a ketone would imply accessibility of the ketone triplet excited state. The reported triplet energy of benzil ($53 kcal mol À1 ), 27 which is the only chromophore present under our conditions, is not high enough to undergo triplet-triplet energy transfer with aliphatic ketones 28 (typically with triplet energies of $80 kcal mol À1 ). 29 Therefore, the ketone triplet state should not be present in any signicant concentration, and a HAT mechanism seems unlikely for both exible and rigid ketones. 30 Conceivably, the benzil triplet state can promote the reaction instead by facilitating electron transfer from the substrate to Selectuor; 31,32 this would result in formation of the wellestablished N-centered radical intermediate. As alternative ways to generate this intermediate, we subjected the linear ketones to our established copper(I)/Selectuor 7a and BEt 3 / Selectuor 8 protocols and found nearly identical uorinated product distributions in each case. Interestingly, when representative rigid cyclic ketones (e.g. starting ketones for compounds 2 and 11) were also subjected to the BEt 3 /Selectuor protocol (in absence of light and a sensitizer), the same selectivity was observed as the visible light-sensitized reaction (Scheme 2). Thus, this putative N-centered radical intermediate is likely the key player in the mechanism for both exible and rigid ketones. As this intermediate is known to be a powerful oxidant, it is possible that an electron transfer (ET) mechanism is operative whereby the ketone assists in proton transfer (PT) instead of HAT. 33 An electron transfer mechanism is also consistent with our observation that the reaction is best suited for our relatively large substrates (with relatively low ionization potentials). Additionally, if the ketone is not properly poised to act as the intramolecular "base," then it is possible other reaction components could act as intermolecular bases (MeCN, the amine derived from Selectuor, etc.), which can explain the loss of selectivity in conformationally exible ketones versus rigid ketones. Lastly, at this time, it is unclear whether the mechanism is concerted (proton-coupled electron transfer, or PCET) or stepwise (electron transfer/proton transfer, or ET/PT) 34 and whether it involves a chain propagation or a closed cycle; we will explore these aspects in future studies.

Conclusions
In summary, this visible light sensitization approach creates an opportunity to use ubiquitous ketones as directing groups in photochemical sp 3 C-H uorination. In a somewhat paradoxical manner, the method is best suited for complex, polycyclic molecules (likely due to increased conformational rigidity); however, its utility as a directed reaction is also demonstrated to be more general. It allows easy access to uorinated products that have not been synthesized previously in good yields and selectivity, and it represents a necessary leap forward in directing radical uorination. Future studies will seek to elucidate the reaction mechanism by exploring the nature of putative electron transfer processes.

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