The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 11, 2024
A mild and efficient electrochemical protocol for the synthesis of quinazolines through N-H/C(sp
Язык: Английский
The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 11, 2024
A mild and efficient electrochemical protocol for the synthesis of quinazolines through N-H/C(sp
Язык: Английский
Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(9), С. 1821 - 1833
Опубликована: Янв. 1, 2024
Metal-free synthesis of medicinally important carbamoylated dihydroquinolinones using readily available, cheap and environment-friendly materials with good to excellent yields.
Язык: Английский
Процитировано
6The Journal of Organic Chemistry, Год журнала: 2025, Номер 90(5), С. 1982 - 1995
Опубликована: Янв. 23, 2025
We report a base-promoted, metal-free multicomponent tandem reaction, involving [4 + 1 1] cycloaddition process between ortho-substituted nitroarenes, aldehydes, and ammonium salts. Modifying the substituents on nitroaromatic compounds effectively provides structurally diverse 2-substituted 4-alkenylquinazolines with good to excellent yields (77%-90% quinazoline 51 examples) high tolerance for various inorganic salts (13 examples, such as NH3·H2O, NH4Cl, NH4HF2). A new method constructing 2,4-substituted selectivity from simple nitrogen source was developed, reaction can be scaled up gram scale. Additionally, this also facilitates preparation of organic molecules photophysical properties, offering insights into further transformation quinazolines.
Язык: Английский
Процитировано
0Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(21), С. 4332 - 4346
Опубликована: Янв. 1, 2024
Visible-light-induced three-component reactions, which were performed under extremely mild conditions without the need for any additional additives and catalysts showed a broad substrate scope, gave corresponding quinazoline-based hybrids in good to excellent yields.
Язык: Английский
Процитировано
1ChemPlusChem, Год журнала: 2024, Номер 89(11)
Опубликована: Июль 18, 2024
Abstract A facile C−H amination of quinazoline employing N ‐fluorobenzenesulfonimide (NFSI) as the source has been disclosed in absence any metal, oxidant or additive. The methodology shows a board range quinazolines with different functional groups moderate to good yields up 87 %. Furthermore, gram‐scale reaction, desulfonylation amine and synthesis pharmaceutical intermediate were also investigated, which demonstrates potential applications medicinal chemistry. plausible mechanism is proposed via F + transfer accompanied by removal one molecule PhSO 2 F. DFT studies experimental work suggest that more favorable than free radical one.
Язык: Английский
Процитировано
1New Journal of Chemistry, Год журнала: 2024, Номер 48(12), С. 5167 - 5172
Опубликована: Янв. 1, 2024
The highly C 6 -regioselective acylation of purines with aldehydes was developed to access -acylated via green radical reactions without metal catalysts or light.
Язык: Английский
Процитировано
0Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(37), С. 7725 - 7735
Опубликована: Янв. 1, 2024
We herein developed an effective approach for the construction of 2- or 4-(1,4-dioxan-2-yl) substituted quinazolines under mild conditions. A silver-K
Язык: Английский
Процитировано
0Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393
Опубликована: Янв. 1, 2024
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 11, 2024
A mild and efficient electrochemical protocol for the synthesis of quinazolines through N-H/C(sp
Язык: Английский
Процитировано
0