Functionalization of Boranes through Thiol/Oxygen Catalysis DOI Creative Commons

Hongyi Tao,

Hairong Lyu

Chinese Journal of Chemistry, Год журнала: 2024, Номер 42(22), С. 2804 - 2810

Опубликована: Июль 17, 2024

Comprehensive Summary A greener and more convenient alternative to traditional methods for the generation of thiyl radical as hydrogen atom transfer (HAT) catalyst is developed, using molecular oxygen oxidize thiol without need chemical initiators or light irradiation. The thiol/oxygen catalysis enables selective efficient difunctionalization borane.

Язык: Английский

Photochemical and Electrochemical Borylation Involving Aryl and Alkyl Compounds DOI Open Access

Linlin Du,

Hua Zhang

Chinese Journal of Organic Chemistry, Год журнала: 2023, Номер 43(5), С. 1726 - 1726

Опубликована: Янв. 1, 2023

Organoboron compounds are important building blocks in organic synthesis and have been widely applied materials pharmaceutical science.The development of practical concise borylation reactions to synthesize organoboron has always one the core topics chemistry.Recently, photochemical electrochemical gained rapid emerged as methods towards compounds.The recent research progress concerning photochemical, photoelectrochemical involving aryl alkyl from view energy resources substrates is reviewed.Additionally, trends this area also discussed.

Язык: Английский

Процитировано

3

Research Progress in Organic Reactions Involving 4-Acyl/Carbamoyl/Alkoxycarbonyl Substituted Hantzsch Esters DOI Open Access
Li Liu, Gang Zheng,

Guoqiang Fan

и другие.

Acta Chimica Sinica, Год журнала: 2023, Номер 81(6), С. 657 - 657

Опубликована: Янв. 1, 2023

In recent years, 4-acyl/carbamoyl/alkoxycarbonyl-substituted Hantzsch esters have been increasingly utilized as a new class of radical precursor reagents, emerging one major research topics for synthetic chemists.These compounds can generate the corresponding acyl, carbamoyl, and alkoxycarbonyl radicals under mild conditions through photochemical, electrochemical, or chemical oxidation systems, leading to wide array addition/coupling reactions.Due reducibility their dihydropyridine skeleton, these precursors often exhibit unique reactivities display good compatibility with transition metal-catalysis organocatalysis systems.In addition, reported reaction typically feature environmental friendliness, highly functional group-tolerance, biocompatibility, which should significant value in fields medicinal chemistry biology.Herein, this review summarizes progress carbamoyl radicals, focuses on generation system, mechanistic underpinnings, well uniqueness applications strategies such esters.

Язык: Английский

Процитировано

3

Site-selective C–H difunctionalization of N-alkyl activated azaarenes via the synergistic catalysis of graphene oxide and visible light DOI

Dehao Duan,

Haiping He, Wei‐Yi Ding

и другие.

Organic Chemistry Frontiers, Год журнала: 2023, Номер 10(24), С. 6055 - 6062

Опубликована: Янв. 1, 2023

Employing heterogeneous cocatalyst-graphene oxide, light-induced site-selective difunctionalizations of pyridiniums/quinoliniums provided straightforward synthetic route toward C4- and C2-phosphonated pyridinone/quinolinone/quinolone cores under air atmosphere.

Язык: Английский

Процитировано

2

Metal-free C–H borylation of heterocycles by merging photoredox and hydrogen atom transfer catalysis DOI

Changfu Wu,

Shuang Luo,

Xiaozu Liu

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(17), С. 4785 - 4793

Опубликована: Янв. 1, 2024

Reported herein is a method that merges organophotoredox and hydrogen atom transfer catalysis to enable the C–H borylation of heterocycles using O 2 as an environmentally friendly oxidant.

Язык: Английский

Процитировано

0

Functionalization of Boranes through Thiol/Oxygen Catalysis DOI Creative Commons

Hongyi Tao,

Hairong Lyu

Chinese Journal of Chemistry, Год журнала: 2024, Номер 42(22), С. 2804 - 2810

Опубликована: Июль 17, 2024

Comprehensive Summary A greener and more convenient alternative to traditional methods for the generation of thiyl radical as hydrogen atom transfer (HAT) catalyst is developed, using molecular oxygen oxidize thiol without need chemical initiators or light irradiation. The thiol/oxygen catalysis enables selective efficient difunctionalization borane.

Язык: Английский

Процитировано

0