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Abstract. We have developed a photoredox-initiated non-decarboxylative C–H fluorination of carboxylic acids. Using Selectfluor as the fluorinating agent, a

The photochemical deracemization of aza-1-isoindolinones has been investigated. A chiral para-methoxy-substituted phenyl ketone was discovered that promotes the conversion of racemic 4-aza-1-isoindoli...

The design of artificial photoenzymes by incorporating synthetic chromophores into proteins represents a promising strategy to achieve non-natural biocatalytic transformations with high levels of ster...

The photocycloaddition of 1,1-dimethylallene to various aromatic carbonyl compounds was found to occur exclusively at the benzene core. While the reaction with methyl 2-methoxybenzoate resulted in a mixture of products resulting from ortho, meta, and para photocycloaddition, acetophenone and its 4-substituted derivatives delivered the respective para photocycloaddition products in 50–58% yields. For 2-methoxyacetophenone, an ortho photocycloaddition initiated a reaction cascade, which led to bicyclic products by the incorporation of a nucleophile in 29–74% yields.

Energy transfer is the key to the successful photocyclization of the title compounds to 3,4-disubstituted 2-azetidinones. If the substituent at the nitrogen atom is primary (R2 = H), trans products a...

Various substituted chromane-2-carboxamides were successfully deracemized by employing a chiral benzophenone (BP, 10 mol%) as photocatalyst and an achiral thiol as additive (20 mol%). The method was ...

Upon catalysis (1 mol %) by a chiral cobalt porphyrin, quinazolinones with a tethered diazo alkane precursor underwent an enantioselective C–H alkylation at carbon atom C4. Formation of five-, six-, a...

Upon catalysis (1 mol %) by a chiral cobalt porphyrin, quinazolinones with a tethered diazo alkane precursor underwent an enantioselective C–H alkylation at carbon atom C4. Formation of five-, six-, a...

Photochemistry opens the possibility to convert a racemic mixture of a chiral compound into a distinct enantiomer in a single operation. Seven chiral phosphoric acids with a pendant thioxanthone chrom...

Carbon dioxide (CO2) is a challenging molecule to incorporate into olefins due to its inherent inert properties. Silanes have now been shown to rapidly react selectively with CO2, catalysed by the…

Chiral heterocyclic lactams have been kinetically resolved in a photochemical process that involves selective hydrogen abstraction by a chiral benzophenone catalyst. Recognition of one enantiomer is ...

Recent studies have shown that energy transfer photoenzymes can be engineered to promote stereocontrolled [2 + 2] cycloadditions; however, existing systems rely on ultraviolet light and display limite...

Chiral spirocyclic oxetanes [2-oxo-spiro(3H-indole-3,2′-oxetanes)] were subjected to irradiation in the presence of a chiral thioxanthone catalyst (5 mol %) at λ = 398 nm. An efficient kinetic resolut...

Carbon dioxide (CO2) is a challenging molecule to incorporate into olefins due to its inherent inert properties. Silanes have now been shown to rapidly react selectively with CO2, catalysed by the presence of a caesium base, to form formate salts which can undergo a hydrogen atom transfer (HAT) to give the d

Cyclohept-2-enone-3-carboxylic acid undergoes a photochemical isomerization from its cis- to its trans-form either upon direct irradiation (λ = 366 nm) or in the presence of a triplet sensitizer (λ =...

4-Substituted 7-(4′-alkenyloxy)-1-indanones were prepared from the respective substituted aryl propanoic acids and subjected to UV-A irradiation (λ = 350 or 366 nm). While the 4-chloro compound was directly converted at λ = 366 nm into a pentacyclic product (47% yield) by a three-photon cascade process, the oxygenated substrates reacted in trifluoroethanol at λ = 350 nm by a two-photon cascade, involving an ortho photocycloaddition, a thermal disrotatory ring opening, and a [4π] photocyclization (six examples, 67–82% yield). An ensuing photochemical di-π-methane rearrangement of the latter products was achieved by irradiation at λ = 350 nm in toluene (five examples, 36–70% yield). The diastereoselectivity of the reaction was probed employing a chiral 1-indanone with a stereogenic center at carbon atom C3. 1-Indanones with a 4-hexenyloxy side chain [(E)- or (Z)-configured] at carbon atom C7 served to interrogate the stereospecifity of the reaction.

ConspectusMillions of chiral compounds contain a stereogenic sp3-hybridized carbon center with a hydrogen atom as one of the four different substituents. The stereogenic center can be edited in an increasing number of cases by selective hydrogen atom transfer (HAT) to and from a photocatalyst. This Account describes the development of photochemical deracemization reactions using chiral oxazole-annulated benzophenones with a bonding motif that allows them to recognize chiral lactam substrates by two-point hydrogen bonding. The backbone of the catalysts consists of a chiral azabicyclo[3.3.1]nonan-2-one with a U-shaped geometry, which enables substrate recognition to occur parallel to the benzoxazole part of the aromatic ketones. The photocatalysts facilitate a catalytic photochemical deracemization of several compound classes including hydantoins, N-carboxyanhydrides, oxindoles, 2,5-diketopiperazines, and 4,7-diaza-1-isoindolinones. In addition, if more than one stereogenic center is present, the editing delivers a distinct diastereoisomer upon the appropriate selection of the respective photocatalyst enantiomer. The chiral photocatalysts operate via the benzophenone triplet that selectively abstracts a properly positioned hydrogen atom in exclusively one of the two substrate enantiomers. The photochemical step creates a planar carbon-centered radical and erases the absolute configuration at this position. While returning HAT to the same position would likely recreate the stereogenic center with the same absolute configuration, spectroscopic and quantum chemical studies suggest that the hydrogen atom is delivered from the photocatalyst to a heteroatom that is in conjugation to the radical center. Two scenarios can be distinguished for the hydrogen atom shuttling process. For hydantoins, N-carboxyanhydrides, and 4,7-diaza-1-isoindolinones, the back HAT occurs to a carbonyl oxygen atom or an imine-type nitrogen atom which is not involved in binding to the catalyst. For oxindoles and 2,5-diketopiperazines, a single lactam carbonyl group in the substrate is available to accept the hydrogen atom. It is currently assumed that back HAT occurs to this group, although the carbonyl oxygen atom is involved in hydrogen bonding to the catalyst. In comparison to the former reaction pathway, the latter process appears to be less efficient and more prone to side reactions. For both cases, an achiral enol or enamine is formed, which delivers upon dissociation from the catalyst statistically either one of the two stereoisomers of the substrate. Since only one substrate enantiomer (or diastereoisomer) is processed, a high enantioselectivity (or diastereoselectivity) results. Even though the editing is a contra-thermodynamic process, the described decoupling of a photochemical and a thermal step allows the usage of a single catalyst in loadings that vary between 2.5 and 10 mol % depending on the specific mode of action.

By coupling a photochemical and a thermal step, a single chiral catalyst can establish a photostationary state in which the enantiopure form of a chiral compound is favored over its racemate. Followin...