Science China Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Янв. 9, 2025
Язык: Английский
Science China Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Янв. 9, 2025
Язык: Английский
Science, Год журнала: 2023, Номер 379(6636), С. 1036 - 1042
Опубликована: Март 10, 2023
Enantioselective redox transformations typically rely on costly transition metals as catalysts and often stoichiometric amounts of chemical agents well. Electrocatalysis represents a more sustainable alternative, in particular through the use hydrogen evolution reaction (HER) place oxidant. In this work, we describe strategies for HER-coupled enantioselective aryl carbon-hydrogen bond (C-H) activation reactions using cobalt precious metal catalyst asymmetric oxidation. Thus, highly nitrogen-hydrogen (C-H N-H) annulations carboxylic amides were achieved, which gave access to point axially chiral compounds. Furthermore, cobalt-mediated electrocatalysis enabled preparation various phosphorus (P)-stereogenic compounds by selective desymmetrization dehydrogenative C-H reactions.
Язык: Английский
Процитировано
168Angewandte Chemie International Edition, Год журнала: 2023, Номер 62(11)
Опубликована: Янв. 20, 2023
In recent years, the merging of electrosynthesis with 3d metal catalyzed C-H activation has emerged as a sustainable and powerful technique in organic synthesis. Despite impressive advantages, development an enantioselective version remains elusive poses daunting challenge. Herein, we report first electrooxidative cobalt-catalyzed enantio- regioselective C-H/N-H annulation olefins using undivided cell at room temperature (up to 99 % ee). t Bu-Salox, rationally designed Salox ligand bearing bulky tert-butyl group ortho-position phenol, was found be crucial for this asymmetric reaction. A strong cooperative effect between Bu-Salox 3,4,5-trichloropyridine enabled highly more challenging α-olefins without secondary bond interactions 96 ee 97 : 3 rr). Cyclovoltametric studies, preparation, characterization, transformation cobaltacycle intermediates shed light on mechanism
Язык: Английский
Процитировано
80Angewandte Chemie International Edition, Год журнала: 2023, Номер 62(21)
Опубликована: Март 20, 2023
Metalla-electrocatalyzed C-H oxygenation represents one of the most straightforward and sustainable approaches to access valuable oxygenated molecules. Despite significant advances, development enantioselective electrochemical reaction is very challenging remains elusive. Herein, we described first CoII -catalyzed alkoxylation. A broad range enantioenriched alkoxylated phosphinamides were obtained in good yields with excellent enantioselectivities (up 98 % yield >99 ee). An unusual cobalt(III) alcohol complex was prepared fully characterized, which proven be a key intermediate this alkoxylation reaction. Mechanistic studies revealed that oxidation CoIII CoIV facilitated by base whole process proceeded through cobalt(III/IV/II) catalytic cycle.
Язык: Английский
Процитировано
63Nature Communications, Год журнала: 2023, Номер 14(1)
Опубликована: Авг. 29, 2023
The N-N atropisomer, as an important and intriguing chiral system, was widely present in natural products, pharmaceutical lead compounds, advanced material skeletons. anisotropic structural characteristics caused by its special axial rotation have always been one of the challenges that chemists strive to overcome. Herein, we report efficient method for enantioselective synthesis axially frameworks via a cobalt-catalyzed atroposelective C-H activation/annulation process. reaction proceeds under mild conditions using Co(OAc)2·4H2O catalyst with salicyl-oxazoline (Salox) ligand O2 oxidant, affording variety products high yields enantioselectivities. This protocol provides approach facile construction atropisomers further expands range derivatives. Additionally, electrocatalysis, desired were also successfully achieved good excellent efficiencies
Язык: Английский
Процитировано
51ACS Catalysis, Год журнала: 2023, Номер 13(7), С. 4250 - 4260
Опубликована: Март 13, 2023
Herein, we disclose an efficient cobalt-catalyzed enantioselective C–H activation and annulation of benzamides with alkenes. This transformation is facilitated via the commercially available cobalt(II) catalyst in presence easily prepared chiral salicyl-oxazoline (Salox) ligand, which provides facile access to (R) or (S) enantiomers dihydroisoquinolone derivatives. It noticeable that reaction proceeded efficiently within extremely short time from 10 30 min under mild conditions. A broad range alkenes bear various functional substituents have been shown good compatibility deliver targeted products high yields enantioselectivities (51 examples, up 98% yield 99% ee). The gram scale experiment removal directing group further demonstrate practicability this protocol potential industrial applications. Density theory calculations elucidate mechanism, spin-state change olefin insertion step accelerates subsequent C–N reductive elimination, identified as stereo-determining step. AIM analysis indicates π interactions are vital for controlling switching stereoselectivity.
Язык: Английский
Процитировано
45ACS Catalysis, Год журнала: 2023, Номер 13(4), С. 2565 - 2575
Опубликована: Фев. 6, 2023
We present herein an unprecedented stereoselective synthesis of triaryl-2-pyrones with monoaxial or contiguous diaxes from readily available starting materials. This N-heterocyclic carbene catalysis method adopts atroposelective annulation 2-aryketones ynals under oxidative conditions. The includes the construction one two axes in a single operation, achieves step economy, and affords axially chiral moderate to good yields, high excellent enantioselectivities. DFT calculations relative energies stereoisomers rotational barriers were performed.
Язык: Английский
Процитировано
42Chemical Communications, Год журнала: 2023, Номер 59(85), С. 12669 - 12684
Опубликована: Янв. 1, 2023
Recent advances in the asymmetric synthesis of axially chiral styrenes catalyzed by transition metals were summarized.
Язык: Английский
Процитировано
42Nature Catalysis, Год журнала: 2024, Номер 7(5), С. 483 - 498
Опубликована: Апрель 30, 2024
Язык: Английский
Процитировано
31Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(10)
Опубликована: Янв. 11, 2024
Transition metal-catalyzed enantioselective C-H carbonylation with carbon monoxide, an essential and easily available C1 feedstock, remains challenging. Here, we disclosed unprecedented catalyzed by inexpensive readily cobalt(II) salt. The reactions proceed efficiently through desymmetrization, kinetic resolution, parallel affording a broad range of chiral isoindolinones in good yields excellent enantioselectivities (up to 92 % yield 99 ee). synthetic potential this method was demonstrated asymmetric synthesis biological active compounds, such as (S)-PD172938 (S)-Pazinaclone. resulting also serve ligands cobalt-catalyzed annulation alkynes construct phosphorus stereocenter.
Язык: Английский
Процитировано
19Chem Catalysis, Год журнала: 2022, Номер 2(11), С. 2965 - 2985
Опубликована: Сен. 16, 2022
Язык: Английский
Процитировано
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