Electrochemical Synthesis of Quinazolines: N–H/C(sp3)–H Coupling of o-Carbonyl Anilines with Amino Acids and Amines DOI
Jiwei Wu,

Lingxiang Yu,

Kaixuan Li

и другие.

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

Metal-free synthesis of carbamoylated dihydroquinolinones via cascade radical annulation of cinnamamides with oxamic acids DOI

Pallav Suman,

Kirti Tomar,

Chandra Shekhar Nishad

и другие.

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

6

Base-Promoted [4 + 1 + 1] Multicomponent Tandem Cycloaddition of Ortho-Substituted Nitroarenes, Aldehydes, and Ammonium Salts To Access 2,4-Substituted Quinazoline Frameworks DOI

Guiyun Zeng,

Juan Wan,

Yilong Yuan

и другие.

The 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

0

Visible-light-induced three-component reactions of α-diazoesters, quinazolinones and cyclic ethers toward quinazoline-based hybrids DOI

Yan Liu,

Qin Yang,

Wei Wang

и другие.

Organic & 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

1

Metal‐Free Regioselective Direct C(4)−H Amination of Quinazoline with N‐fluorobenzenesulfonimide DOI
Yong Wang,

Xueying Lin,

Xianyu Ying

и другие.

ChemPlusChem, 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

1

Metal-free, direct acylation of purines to access C6-acylated purine derivatives induced by TBHP via Minisci-type reaction DOI

Chunhui Zou,

Mingwu Yu,

Zhongkai Jiang

и другие.

New 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

0

Ag-Catalyzed Cross-Dehydrogenative-Coupling for the Synthesis of 1,4-Dioxan-2yl Substituted Qunazoline Hybrids in Aqueous Media DOI

Xixian Liu,

Dayu Xie,

Qin Yang

и другие.

Organic & 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

0

Six-membered ring systems: Diazines and benzo derivatives DOI

K. Alison Rinderspacher

Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393

Опубликована: Янв. 1, 2024

Процитировано

0

Electrochemical Synthesis of Quinazolines: N–H/C(sp3)–H Coupling of o-Carbonyl Anilines with Amino Acids and Amines DOI
Jiwei Wu,

Lingxiang Yu,

Kaixuan Li

и другие.

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

Процитировано

0