Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(7), С. 2063 - 2063
Опубликована: Янв. 1, 2024
Язык: Английский
Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(7), С. 2063 - 2063
Опубликована: Янв. 1, 2024
Язык: Английский
Journal of the American Chemical Society, Год журнала: 2025, Номер unknown
Опубликована: Янв. 29, 2025
Due to their strong aromaticity and difficulties in chemo-, regio-, enantioselectivity control, asymmetric hydrogenation of naphthol derivatives 1,2,3,4-tetrahydronaphthols has remained a long-standing challenge. Herein, we report the first example homogeneous catalyzed by tethered rhodium-diamine catalysts, affording wide array optically pure high yields with excellent enantioselectivities (up 98% yield >99% ee). Mechanistic studies experimental computational approaches reveal that fluorinated solvent 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) plays vital roles control reactivity selectivity, 1-naphthol is reduced via cascade reaction pathway, including dearomative tautomerization, 1,4-hydride addition, 1,2-hydride addition sequence. A novel synergistic activation mode was proposed which HFIP assists both hydrogen molecule presence base, situ-generated fleeting keto tautomer immediately trapped Rh(III)-H species before it escapes from cage. This protocol provides straightforward practical pathway for synthesis key intermediates several chiral drugs. Particularly, Nadolol, drug treatment hypertension, angina pectoris, congestive heart failure, certain arrhythmias, enantioselectively synthesized time.
Язык: Английский
Процитировано
1Organic Letters, Год журнала: 2025, Номер unknown
Опубликована: Март 11, 2025
The asymmetric trans-selective hydrogenation of arenes has long been a significant challenge. In this work, we were able to control the trans/cis selectivity in ruthenium-catalyzed 2,3-disubstituted quinoxalines by varying catalyst counteranion. Using density functional theory calculations, investigated weak interactions─such as CH/π and hydrogen bonding─among counteranion, framework, substrate, elucidating fundamental influence counteranions on quinoxalines.
Язык: Английский
Процитировано
0Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(7), С. 2063 - 2063
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
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