2024
DOI: 10.1039/d4cc00181h
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Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C–H activation

Mikhail A. Boym,
Roman A. Pototskiy,
Evgeniya S. Podyacheva
et al.

Abstract: Heating tert-butyl-tetraline with [(p-cymene)RuCl2]2 produces the racemic complex [(arene)RuCl2]2, which can be separated into enantiomers by chromatography of its diastereomeric adducts with chiral phosphine ligand. The resolved chiral complex catalyzes...

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Cited by 4 publications
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“…[14] During the submission of our manuscript, they reported the synthesis of a planar chiral arene ruthenium complex which could catalyzed the asymmetric CÀ H activation of N-methoxy-benzamides with Nvinyl-amides to afford 3-amino-dihydroisoquinolones in 50-90 % yield with 40-80 % ee. [15] Despite excellent performance of chiral [2.2]paracyclophane ruthenium catalysts in our previous work, they exhibited poor enantioselectivity in many other reactions that we have tried. It is most likely due to their shallow chiral pockets.…”
mentioning
confidence: 80%
“…[14] During the submission of our manuscript, they reported the synthesis of a planar chiral arene ruthenium complex which could catalyzed the asymmetric CÀ H activation of N-methoxy-benzamides with Nvinyl-amides to afford 3-amino-dihydroisoquinolones in 50-90 % yield with 40-80 % ee. [15] Despite excellent performance of chiral [2.2]paracyclophane ruthenium catalysts in our previous work, they exhibited poor enantioselectivity in many other reactions that we have tried. It is most likely due to their shallow chiral pockets.…”
mentioning
confidence: 80%