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We report herein a rare example of enantiodivergent aldehyde addition with β‐alkenyl allylic boronates via chiral Brønsted acid catalysis. 2,6‐Di‐9‐anthracenyl‐substituted chiral phosphoric acid‐catalyzed asymmetric allylation using β‐vinyl substituted allylic boronate gave alcohols with R absolute configuration. The sense of asymmetric induction of the catalyst in these reactions is opposite to those in prior reports. Moreover, in the presence of the same acid catalyst, the reactions with β‐2‐propenyl substituted allylic boronate generated homoallylic alcohol products with S absolute configuration. Unusual substrate‐catalyst C−H⋅⋅⋅π interactions in the favoured reaction transition state were identified as the origins of observed enantiodivergence through DFT computational studies. [ABSTRACT FROM AUTHOR]

We report herein a rare example of enantiodivergent aldehyde addition with β‐alkenyl allylic boronates via chiral Brønsted acid catalysis. 2,6‐Di‐9‐anthracenyl‐substituted chiral phosphoric acid‐catalyzed asymmetric allylation using β‐vinyl substituted allylic boronate gave alcohols with R absolute configuration. The sense of asymmetric induction of the catalyst in these reactions is opposite to those in prior reports. Moreover, in the presence of the same acid catalyst, the reactions with β‐2‐propenyl substituted allylic boronate generated homoallylic alcohol products with S absolute configuration. Unusual substrate‐catalyst C−H⋅⋅⋅π interactions in the favoured reaction transition state were identified as the origins of observed enantiodivergence through DFT computational studies. [ABSTRACT FROM AUTHOR]

Computations and experiments leading to new chiral phosphoric acids (CPAs) for epoxide thionations are reported. Density functional theory calculations reveal the mechanism and origin of the enantioselectivity of such CPA‐catalyzed epoxide thionations. The calculated mechanistic information was used to design new efficient CPAs that were tested experimentally and found to be highly effective. Bulky ortho‐substituents on the 3,3′‐aryl groups of the CPA are important to restrict the position of the epoxide in the key transition states for the enantioselectivity‐determining step. Larger para‐substituents significantly improve the enantioselectivity of the reaction. [ABSTRACT FROM AUTHOR]

Computations and experiments leading to new chiral phosphoric acids (CPAs) for epoxide thionations are reported. Density functional theory calculations reveal the mechanism and origin of the enantioselectivity of such CPA‐catalyzed epoxide thionations. The calculated mechanistic information was used to design new efficient CPAs that were tested experimentally and found to be highly effective. Bulky ortho‐substituents on the 3,3′‐aryl groups of the CPA are important to restrict the position of the epoxide in the key transition states for the enantioselectivity‐determining step. Larger para‐substituents significantly improve the enantioselectivity of the reaction. [ABSTRACT FROM AUTHOR]

Hydrogenation of alkenes is one of the most fundamental transformations in organic synthesis, and widely used in the petrochemical, pharmaceutical, and food industries. Although numerous hydrogenation methods have been developed, novel types of catalysis with new mechanisms and new hydrogen sources are still desirable. Thioxanthone (TX) is widely used in energy‐transfer photoreactions, but rarely in photoredox processes. Herein we show that a catalytic amount of TfOH as a co‐catalyst can tune the properties of TX to make it a photoredox catalyst with highly enhanced oxidative capability in the hydrogenation of carbonylated alkenes with the cheap petroleum industrial product p‐xylene serving as the hydrogen source. Deuterium can also be introduced by this method by using D2O as the D source. To the best of our knowledge, this is the first example of using p‐xylene as a hydrogen source. [ABSTRACT FROM AUTHOR]

Hydrogenation of alkenes is one of the most fundamental transformations in organic synthesis, and widely used in the petrochemical, pharmaceutical, and food industries. Although numerous hydrogenation methods have been developed, novel types of catalysis with new mechanisms and new hydrogen sources are still desirable. Thioxanthone (TX) is widely used in energy‐transfer photoreactions, but rarely in photoredox processes. Herein we show that a catalytic amount of TfOH as a co‐catalyst can tune the properties of TX to make it a photoredox catalyst with highly enhanced oxidative capability in the hydrogenation of carbonylated alkenes with the cheap petroleum industrial product p‐xylene serving as the hydrogen source. Deuterium can also be introduced by this method by using D2O as the D source. To the best of our knowledge, this is the first example of using p‐xylene as a hydrogen source. [ABSTRACT FROM AUTHOR]

Chiral tetrahydrothiophenes and tetrahydroselenophenes are highly useful structural units. Described here is a new catalytic asymmetric approach for their synthesis. With a suitable chiral Brønsted acid catalyst, an oxetane desymmetrization by a well‐positioned internal sulfur or selenium nucleophile proceeded efficiently to generate all‐carbon quaternary stereocenters with excellent enantioselectivities. Taming the sulfur and selenium nucleophile in the form of a thioester and selenoester, respectively, is crucial to the success of this work. This approach also allows the facile synthesis of chiral tetrahydrothiopyrans. Mechanistic studies, including DFT calculations, suggested an intramolecular acyl‐transfer pathway. Utilities of the chiral products are also demonstrated. [ABSTRACT FROM AUTHOR]