Copper-catalyzed amination of arene DOI

Xiaobin Tan,

Wanqing Wu, Huanfeng Jiang

и другие.

Scientia Sinica Chimica, Год журнала: 2022, Номер 53(3), С. 410 - 422

Опубликована: Ноя. 26, 2022

Aromatic amines are widely used in the fields of natural products, pharmaceutical chemistry and materials science, thus new methods metal-catalyzed C–N bond coupling for constructing aromatic always have been focus attention chemists scientific community. Copper, as a catalyst amination arenes, has attracted extensive due to its unique catalytic performance variety oxidation states. In this review, recent progress construction compounds C(sp2)–N catalyzed by copper is reviewed, reaction mechanisms representative reactions briefly described.

Язык: Английский

Electrochemical N-acylation and N-α-ketoacylation of sulfoximines via the selective decarboxylation and dehydration of α-ketoacids DOI
Chen Kang, Mingzhe Li, Wenxiu Huang

и другие.

Green Chemistry, Год журнала: 2023, Номер 25(21), С. 8838 - 8844

Опубликована: Янв. 1, 2023

We describe an electrochemical N -acylation and -α-ketoacylation of sulfoximines via the selective decarboxylation dehydration α-ketoacids using electricity as a “traceless” oxidant α-ketoacid “acyl” or “α-ketoacyl” source.

Язык: Английский

Процитировано

11

Cobalt(III)-Catalyzed Directed C-7 Selective C–H Alkynylation of Indolines with Bromoalkynes DOI
Ruihan Niu, Jing Zhang, Ruyuan Zhao

и другие.

Organic Letters, Год журнала: 2023, Номер 25(29), С. 5411 - 5415

Опубликована: Июль 17, 2023

A cobalt(III)-catalyzed directed C-7 alkynylation of indolines with easily accessible bromoalkynes has been developed. The reaction a broad substrate scope excellent yields and represents powerful route to the synthesis 7-alkynyl-substituted indolines. In addition, can be extended coupling N-aryl 7-azaindoles, highlighting synthetic practicability strategy.

Язык: Английский

Процитировано

10

Pd-Catalyzed C-7 Arylation of Indolines with Aryltriazenes under Mild Conditions DOI
Jianan Gao,

Qinglang Song,

Lin Zhang

и другие.

The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(15), С. 11056 - 11068

Опубликована: Июль 18, 2023

A palladium-catalyzed direct C-H arylation of indolines at C-7 position has been achieved near-ambient temperature. The reaction was carried out with aryltriazene as a stable aryl source and electron shuttle to sustainably release radical in situ under the action promoter, pyrimidine detachable directing group for synthesis 7-arylindolines oxidant- ligand-free conditions. Notably, this catalytic system can also be applied site-selective tetrahydroquinolines (C-8) carbazoles (C-1).

Язык: Английский

Процитировано

9

Oxidative Nickel-Catalyzed ortho-C–H Amination of (Iso)quinolines with Alicyclic Amines Directed by a Sacrificial N-Oxide Group DOI

Weiqi Zhu,

Wei Min,

Yanrui Wang

и другие.

Organic Letters, Год журнала: 2024, Номер 26(4), С. 912 - 916

Опубликована: Янв. 25, 2024

Transition metal (TM)-catalyzed direct amination of C–H bonds on free or fused pyridine (Py) rings with amines still remains scarce because and the Py ring tend to adopt a nonproductive N-bound coordination many TMs, leading significant decrease catalytic reactivity. We herein disclose nickel-catalyzed sacrificial N-oxide group directed oxidative coupling (iso)quinolyl alicyclic amines, which furnishes bioimportant amino(iso)quinolines efficiently selectively in single step. Noteworthy, this protocol avoids use aggressive reactants very strong bases usually required when aminating nonoxidized rings.

Язык: Английский

Процитировано

2

Ru(II)‐Catalyzed ortho C—H Allylation of N‐Aryl‐7‐azaindoles with 2‐Methylidene Cyclic Carbonate DOI
Jing Zhang,

Quanjian Luo,

Han‐Chi Wang

и другие.

Chinese Journal of Chemistry, Год журнала: 2023, Номер 42(9), С. 985 - 989

Опубликована: Дек. 26, 2023

Comprehensive Summary A Ru(II)‐catalyzed ortho allylation reaction of N ‐aryl‐7‐azaindole with readily available 2‐methylidene cyclic carbonate has been developed. This is an effective pathway for synthesizing 7‐azaindole derivatives a wide scope substrates and high yields. In addition, the method can be extended to other heterocyclic compounds several carbonates, highlighting practicality this strategy synthesis.

Язык: Английский

Процитировано

4

Cobalt-Catalyzed Regioselective C8–H Sulfoxamination of 1-Naphthylamine Derivatives with NH-Sulfoximines DOI

Nileshkumar B. Rathod,

Raj N. Patel,

Sachinkumar D. Patel

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 18, 2024

A simple cobalt-catalyzed, picolinamide-directed C8–H sulfoxamination of 1-naphthalamides with NH-sulfoximines has been developed. This cross-dehydrogenative C–H/N–H coupling reaction offers a facile route to N-arylated sulfoximines, exhibiting high yields, broad substrate scope, and excellent functional group tolerance scalability.

Язык: Английский

Процитировано

1

Copper-catalyzed amination of arene DOI

Xiaobin Tan,

Wanqing Wu, Huanfeng Jiang

и другие.

Scientia Sinica Chimica, Год журнала: 2022, Номер 53(3), С. 410 - 422

Опубликована: Ноя. 26, 2022

Aromatic amines are widely used in the fields of natural products, pharmaceutical chemistry and materials science, thus new methods metal-catalyzed C–N bond coupling for constructing aromatic always have been focus attention chemists scientific community. Copper, as a catalyst amination arenes, has attracted extensive due to its unique catalytic performance variety oxidation states. In this review, recent progress construction compounds C(sp2)–N catalyzed by copper is reviewed, reaction mechanisms representative reactions briefly described.

Язык: Английский

Процитировано

0