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Ruthenium-Catalyzed Carbocycle-Selective Hydrogenation of Fused Heteroarenes

Chenguang Luo, Chao Wu, Xiaoming Wang, Zhaobin Han, Zheng Wang, Kuiling Ding

2024Journal of the American Chemical Society25 citationsDOIOpen Access PDF

Abstract

The homogeneous catalytic hydrogenation of benzo-fused heteroarenes generally provides partially hydrogenated products wherein the heteroaryl ring is preferentially reduced, such as quinoline hydrogenation, leading to 1,2,3,4-tetrahydroquinoline. Herein, we report a carbocycle-selective hydrogenation of fused N -heteroarenes (quinoline, isoquinoline, quinoxaline, etc.) using the Ru complex of a chiral spiroketal-based diphosphine (SKP) as the catalyst, affording the corresponding 5,6,7,8-tetrahydro products in high chemoselectivities. This catalytic system is also effective for the asymmetric carbocycle hydrogenation of fused heteroarenes bearing a boryl or amino group. Experimental studies provided a strong support for the homogeneous nature of the catalysis, and an inner-sphere mechanism was proposed for the hydrogenation. DFT calculations indicated that the hydrogenation is initiated by η 4 -coordinative activation of quinoline carbocycle to Ru dihydride complex of SKP, followed by metal-to-ligand hydride transfer. Subsequent carbocycle reduction proceeds via consecutive steps of the H 2 oxidative addition and C–H reductive elimination.

Topics & Concepts

ChemistryRutheniumCatalysisQuinolineHomogeneousCatalytic hydrogenationRing (chemistry)Noyori asymmetric hydrogenationHomogeneous catalysisCombinatorial chemistryMedicinal chemistryOrganic chemistryPhysicsThermodynamicsAsymmetric Hydrogenation and CatalysisNanomaterials for catalytic reactionsCatalysis and Hydrodesulfurization Studies
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