Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 421 - 484
Опубликована: Янв. 1, 2024
Язык: Английский
Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 421 - 484
Опубликована: Янв. 1, 2024
Язык: Английский
Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(12), С. 2324 - 2338
Опубликована: Янв. 1, 2024
This review summarizes the most recent progress made in C–H bond activation-initiated spiroannulation reactions and their applications construction of structurally diverse biologically valuable spirocyclic scaffolds.
Язык: Английский
Процитировано
21Tetrahedron, Год журнала: 2025, Номер unknown, С. 134552 - 134552
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 14, 2025
An efficient Rh(III)-catalyzed annulation between 3-aryl-2H-benzo[b][1,4]oxazines and α-diazo-β-ketoesters was developed, affording a series of polycyclic heteroarenes in moderate to excellent yields with good functional group compatibility. The procedure featured high efficiency, redox neutrality, twofold ortho-C-H activation, dual [4 + 2] annulation. Moreover, several important intermediates products have been isolated as powerful evidence for the proposed reaction mechanism.
Язык: Английский
Процитировано
0New Journal of Chemistry, Год журнала: 2024, Номер 48(18), С. 8243 - 8276
Опубликована: Янв. 1, 2024
The present review summarizes the recent advances (2018–2023) in stereoselective annulation involving p -benzoquinones for construction of fused, spiro and bridged/cage frameworks.
Язык: Английский
Процитировано
1Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(7), С. 2223 - 2223
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
1Asian Journal of Organic Chemistry, Год журнала: 2023, Номер 12(12)
Опубликована: Ноя. 10, 2023
Abstract Pivaloyl‐directed Rh(III)‐catalyzed regioselective C7 Ar ‐H functionalization of protected tryptophans were accomplished with 1,4‐benzoquinones, furnishing a series quinone‐appended tryptophan‐based unnatural amino acids in high yields. Further, the late stage on tryptophan‐containing dipeptides was achieved 1,4‐benzoquinones moderate reactivity.
Язык: Английский
Процитировано
2Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 22(5), С. 998 - 1009
Опубликована: Дек. 26, 2023
An efficient Ru( ii )-catalyzed C–H activation-based spiroannulation of benzoxazines with easily available benzoquinone and N -sulfonyl quinone monoimine has been realized, providing a straightforward strategy to access NH-containing spiropyrans.
Язык: Английский
Процитировано
2Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 421 - 484
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
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