Cyclization of Azobenzenes Via Electrochemical Oxidation Induced Benzylic Radical Generation DOI
Anni Li, Xiangyi Li, Fang Ma

et al.

Organic Letters, Journal Year: 2023, Volume and Issue: 25(32), P. 5978 - 5983

Published: Aug. 7, 2023

An electrochemical oxidation-induced cyclization of ortho-alkyl-substituted azobenzenes has been developed. The direct benzylic C-H functionalization with respect to could proceed in the absence any catalyst or external chemical oxidant afford a number 2H-indazole derivatives moderate good yields. This protocol enables reuse byproduct same 2H-indazoles, thus significantly reducing pollution discharge synthetic chemistry.

Language: Английский

Cu(ii)-catalyzed domino construction of spironaphthalenones by dearomatization of β-naphthols and using N,N-dimethylaminoethanol as a C1 synthon DOI

Meiqi Geng,

Jinqiang Kuang, Maozhong Miao

et al.

Organic & Biomolecular Chemistry, Journal Year: 2023, Volume and Issue: 21(15), P. 3101 - 3104

Published: Jan. 1, 2023

Herein, a Cu(II)-catalyzed facile construction of synthetically valuable spiro compounds from β-naphthols in air is reported, which N,N-dimethylaminoethanol (DMEA) serves as an efficient and unique C1 synthon. This transformation proceeds through ortho-quinone methide (o-QM) formation/Michael addition/dearomatization sequence, affording various spiro(naphthalenenaphtho)furan-2-ones moderate to excellent yields.

Language: Английский

Citations

24

Copper‐Catalyzed Radical Silylarylation of Activated Alkenes: Preparation of β‐Silyl Amide‐Pharmaceutical Hybrids DOI
Fei Chen, Shiyu Liu, Li Xiao

et al.

Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(6), P. 1325 - 1330

Published: Feb. 2, 2024

Abstract Copper‐catalyzed silylarylation of N ‐(arylsulfonyl)acrylamides via a tandem silyl radical addition/1,4‐aryl migration/desulfonylation sequence has been developed. This method employs silanes as the precursor and di‐ tert ‐butyl peroxide (DTBP) initiator. By using this cascade procedure, series β ‐silyl amide‐pharmaceutical hybrids which contain an α ‐all‐carbon quaternary stereocenter were facilely synthesized.

Language: Английский

Citations

9

Recent Advances on C—H Functionalization via Oxidative Electrophotocatalysis DOI

Aman Hasil,

Rui Chang,

Juntao Ye

et al.

Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(3), P. 728 - 728

Published: Jan. 1, 2024

Language: Английский

Citations

8

Electrochemical Silylation of Electron‐Deficient Heterocycles Using N‐Hydroxyphthalimide as HAT Catalyst DOI
Cong Jiang, Yujie Liao, Heng Li

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(8), P. 1205 - 1210

Published: March 22, 2023

Abstract A practical electrochemical Minisci‐type reaction for the synthesis of silylated heterocycles is described. Using N ‐hydroxyphthalimide (NHPI) as hydrogen atom transfer (HAT) catalyst and trialkylsilanes silyl radical sources, a wide range electron‐deficient in‐cluding quinoline, quinoxaline, phthalazine, 3,6‐dichloropyridazine, phenanthridine, 6‐chloroimidazo[1,2‐ b ]pyridazine coumarin, etc. were easily converted to corresponding products in 37–83% yields. magnified image

Language: Английский

Citations

14

Cyclization of Azobenzenes Via Electrochemical Oxidation Induced Benzylic Radical Generation DOI
Anni Li, Xiangyi Li, Fang Ma

et al.

Organic Letters, Journal Year: 2023, Volume and Issue: 25(32), P. 5978 - 5983

Published: Aug. 7, 2023

An electrochemical oxidation-induced cyclization of ortho-alkyl-substituted azobenzenes has been developed. The direct benzylic C-H functionalization with respect to could proceed in the absence any catalyst or external chemical oxidant afford a number 2H-indazole derivatives moderate good yields. This protocol enables reuse byproduct same 2H-indazoles, thus significantly reducing pollution discharge synthetic chemistry.

Language: Английский

Citations

14