(Invited, Digital Presentation) Carbocation Generation By Organophotoredox Catalyzed Radical-Polar Crossover

Abstract

Carbocation is one of the most common and reactive chemical species in organic chemistry, which has been broadly utilized for alkylation of various nucleophiles and rearrangement reaction. Conventionally, carbocation is generated from alkyl electrophiles or alkenes in the presence of strong Lewis acids and Brønsted acids, which narrows usable nucleophiles and coexistable functional groups. The requirement of strong acidic conditions would originate from the difficulty of two electron abstraction from carbocation precursors at once. Recently, to solve this problem, activation of substrates via single electron transfer was presented. Knowles and co-workers reported the carbocation generation from the mesolytic cleavage of alkoxyamine-derived radical cation, that is generated by a visible-light mediated photoredox catalysis. Although this protocol does not require the strong acids, the low accessibility of alkoxyamine substrates restricted the introducible alkyl groups. In this presentation, a new approach to catalytic generation of carbocation by a visible light-mediated organophotoredox catalysis is provided. We were interested in an organocatalysis merging with the radical-polar crossover (RPC) mechanism as an approach to non-acidic and catalytic generation of carbocations. Details of our scenario for the RPC are described in Figure. We selected N-Ph-benzo[b]phenothiazine (PTH) as a suitable organophotoredox RPC catalyst due to three features: excitation in the UV-visible area, high reduction potential and potential persistent properties of the corresponding radical cation. Aliphatic carboxylic acid-derived redox active esters were chosen as carbocation precursors due to the availability and the well-studied reactivity. The catalytic system is initiated by single electron transfer from a phenothiazine catalyst to a redox active ester under irradiation of a blue light-emitting diode (LED) to generate the radical cation form of the catalyst (A) and an alkyl radical (B). Then, recombination process between A and B affords an alkylsulfonium intermediate C, which acts as a carbocation equivalent. The carbocation equivalent was applied to alkylation of various nucleophiles and the semipinacol rearrangement reactions. First, the catalytic system was exploited to alkylation of various nucleophiles. After screening of reaction conditions, the combination of N-phenyl benzo[b]phenothiazine and lithium tetrafluoroborate was found to be effective in this alkylation protocol. Aliphatic alcohol, water, amide, thiol, fluoride anion and allylsilane could participate in this organophotoredox catalysis as nucleophiles. This protocol allowed to use secondary or tertiary aliphatic carboxylic acid-derived redox active esters as alkylating reagents, providing sterically hindered molecules with functional group compatibility.Subsequently, we applied the photochemically-generated carbocation equivalent to the semipinacol rearrangement reaction. Although the semipinacol rearrangement reaction has been utilized in key steps for construction of complex carbon frameworks in total synthesis of natural products, the conventional methods require specific design of the substrates and harsh reaction conditions to control the reactivity and regioselectivity. Since our method has the advantage of using carboxylic acids as the carbocation precursors, the substrates are easily synthesized from the corresponding enolate species derived from aliphatic carboxylic acids and carbonyl compounds. Then, we found the b-hydroxy redox active ester derivatives underwent the decarboxylative semipinacol rearrangement reaction, affording the complex carbonyl compounds. For example, the reaction with substrate prepared from aromatic aldehyde and secondary aliphatic carboxylic acid proceeded to give the aldehyde bearing an a-quaternary carbon center through migration of the aromatic ring. The reactions with cyclic ketone-derived substrates also occurred to furnish the ring expansion products. Figure 1