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Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C–H activation
Chemical Communications ( IF 4.9 ) Pub Date : 2024-03-26 , DOI: 10.1039/d4cc00181h
Mikhail A. Boym 1, 2 , Roman A. Pototskiy 1 , Evgeniya S. Podyacheva 1, 2 , Denis A. Chusov 1, 2 , Yulia V. Nelyubina 1, 3 , Dmitry S. Perekalin 1, 2
Affiliation  

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 C–H activation of N-methoxy-benzamides and their annulation with N-vinyl-pivaloyl amide giving dihydroisoquinolones in 50–80% yields and with 40–80% enantiomeric excess.

中文翻译:

平面手性芳烃钌配合物:合成、对映异构体的分离以及催化C-H活化的应用

叔丁基四氢萘与[( p-伞花烃)RuCl 2 ] 2加热生成外消旋络合物[(芳烃)RuCl 2 ] 2,可通过其与手性膦配体的非对映加合物的色谱法将其分离成对映体。解析的手性配合物催化N-甲氧基-苯甲酰胺的 C-H 活化,并与N-乙烯基-新戊酰酰胺成环,生成二氢异喹诺酮,产率为 50-80%,对映体过量为 40-80%。
更新日期:2024-03-26
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