Electrochemical Selenocyclization of N-Alkyl anilines: Access to 3-Selenyl quinolines DOI

Longqiang Zhao,

Huimin Li,

Mengyu Peng

и другие.

Tetrahedron, Год журнала: 2024, Номер unknown, С. 134257 - 134257

Опубликована: Сен. 1, 2024

Язык: Английский

Nucleophilic Substitution at Unactivated Arene C–H: Copper-Catalyzed anti-Selective Silylative Cyclization of Substituted Benzylacetylenes DOI

Hirokazu Moniwa,

Ryo Shintani

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Фев. 13, 2025

A new mode of carbon-carbon bond formation via electrophilic activation a C-H has been developed in the context copper-catalyzed anti-selective silylative cyclization benzylacetylenes with silylboronates for synthesis 2-silyl-1H-indenes. The reaction proceeds high regioselectivity various substituted benzylacetylenes, and resulting products could be further functionalized. arene that undergoes acts as an electrophile release hydride under redox neutral conditions, mechanism was probed by deuterium-labeling experiments density functional theory calculations.

Язык: Английский

Процитировано

1

Palladium-Catalyzed (3 + 2) Annulation of Aromatic Acids by C(sp3)–H Olefination and Decarboxylative Cross-Coupling Reaction DOI
Xiaobo Xu, Yangyang Wang, Xiao Yu

и другие.

Organic Letters, Год журнала: 2024, Номер 26(7), С. 1338 - 1342

Опубликована: Фев. 9, 2024

A palladium-catalyzed (3 + 2) annulation of 2-methylbenzoic acid with maleimide using Ac-Leu-OH as a powerful ligand has been reported. Through site-selective γ-C(sp3)–H olefination reaction and sequential decarboxylative cross-coupling reaction, five-membered cyclic ring was obtained the final product. This novel features great site selectivity reactivity to generate various products in moderate good yields.

Язык: Английский

Процитировано

6

Palladium-Catalyzed Annulation of Tertiary Anilines with 3-Butenoic Acid via Dual C–H Bond Activation DOI
Jinhui Zhang, Chao Liu, Jiahao Wu

и другие.

Organic Letters, Год журнала: 2024, Номер 26(21), С. 4422 - 4426

Опубликована: Май 20, 2024

Catalytic cyclization via dual C-H bond activation has evolved as a powerful strategy for building bi- and polycyclic molecules. Herein, palladium-catalyzed annulation of tertiary anilines with 3-butenoic acid

Язык: Английский

Процитировано

1

CuBr2 Mediated Dehydrogenative [4 + 2] Annulation of 1-Naphthyl-1,3-indandiones and Alkenes DOI
Xu Zhang,

Mengfan Chang,

Tongtong Ni

и другие.

Chemical Communications, Год журнала: 2024, Номер 60(68), С. 9070 - 9073

Опубликована: Янв. 1, 2024

Intermolecular annulation reactions of 1-naphthyl-1,3-indandiones with alkenes proceed efficiently in the presence a copper catalyst to generate spirocarbocycle compounds.

Язык: Английский

Процитировано

1

A New Method of Constructing Methyleneindene and Quinoline Frameworks from Methylenecyclopropanes DOI

Qu‐Hang Yang,

Min Shi, Yin Wei

и другие.

Chemistry - An Asian Journal, Год журнала: 2024, Номер 19(15)

Опубликована: Май 9, 2024

In this paper, we have established an operationally convenient protocol for the rapid construction of polysubstituted methyleneindene and quinoline derivatives under mild conditions. This new synthetic method is achieved through conversion acetyl-substituted methylenecyclopropanes with TsOH ⋅ H

Язык: Английский

Процитировано

0

De novo synthesis of atropisomeric benzofurans via Cu/SPDO complex catalyzed asymmetric formal [3 + 2] annulation DOI

Fan‐Xiao Meng,

Xingyu Wang,

Ka Lu

и другие.

Science China Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 9, 2024

Язык: Английский

Процитировано

0

Electrochemical Selenocyclization of N-Alkyl anilines: Access to 3-Selenyl quinolines DOI

Longqiang Zhao,

Huimin Li,

Mengyu Peng

и другие.

Tetrahedron, Год журнала: 2024, Номер unknown, С. 134257 - 134257

Опубликована: Сен. 1, 2024

Язык: Английский

Процитировано

0