Three-component three-bond forming cascade via palladium photoredox catalysis DOI Creative Commons
Peter Bellotti, Maximilian Koy,

Christian Gutheil

и другие.

Chemical Science, Год журнала: 2020, Номер 12(5), С. 1810 - 1817

Опубликована: Дек. 8, 2020

A highly modular radical cascade strategy based upon cyclisation/allylic substitution sequence between alkyl/aryl bromides, 1,3-dienes and nucleophiles ranging from sulfinates to amines, phenols 1,3-dicarbonyls is described (>80 examples). Palladium phosphine complexes - which merge properties of photo- cross coupling-catalysts allow forge three bonds with complete 1,4-selectivity stereocontrol, delivering value added carbocyclic heterocyclic motifs that can feature

Язык: Английский

Metal-catalyzed radical-type transformation of unactivated alkyl halides with C–C bond formation under photoinduced conditions DOI
S. Ye,

Tianyi Xiang,

Xiaofang Li

и другие.

Organic Chemistry Frontiers, Год журнала: 2019, Номер 6(13), С. 2183 - 2199

Опубликована: Янв. 1, 2019

Recent advances in the metal-catalyzed radical-type transformation of unactivated alkyl halides with C–C bond formation under photoinduced conditions are summarized. Usually, a broad reaction scope is observed including tertiary, secondary, and primary halides, good functional group compatibility.

Язык: Английский

Процитировано

101

Visible‐Light‐Induced Palladium‐Catalyzed Generation of Aryl Radicals from Aryl Triflates DOI Creative Commons

Maxim Ratushnyy,

Nikita Kvasovs,

Sumon Sarkar

и другие.

Angewandte Chemie International Edition, Год журнала: 2020, Номер 59(26), С. 10316 - 10320

Опубликована: Март 10, 2020

Abstract A mild visible‐light‐induced Pd‐catalyzed intramolecular C−H arylation of amides is reported. The method operates by cleavage a C(sp 2 )−O bond, leading to hybrid aryl Pd‐radical intermediates. following 1,5‐hydrogen atom translocation, cyclization, and rearomatization steps lead valuable oxindole isoindoline‐1‐one motifs. Notably, this provides access products with readily enolizable functional groups that are incompatible traditional conditions.

Язык: Английский

Процитировано

99

Visible Light-induced Palladium-catalysis in Organic Synthesis DOI Open Access
Wen‐Jun Zhou,

Guang‐Mei Cao,

Zhan-Peng Zhang

и другие.

Chemistry Letters, Год журнала: 2019, Номер 48(3), С. 181 - 191

Опубликована: Янв. 22, 2019

Palladium-catalyzed carbon-carbon and carbon-heteroatom bond construction are among the most significant powerful methods in organic synthesis. Numerous investigations focusing on appli...

Язык: Английский

Процитировано

93

Synthesis of Oxazolidin‐2‐ones from Unsaturated Amines with CO2 by Using Homogeneous Catalysis DOI
Zhen Zhang, Jian‐Heng Ye, Dongshan Wu

и другие.

Chemistry - An Asian Journal, Год журнала: 2018, Номер 13(17), С. 2292 - 2306

Опубликована: Июнь 1, 2018

Carbon dioxide (CO2 ), a well-known greenhouse gas, is also nontoxic, readily accessible, and renewable one-carbon (C1) source. However, owing to its thermodynamic stability kinetic inertness, the efficient utilization of CO2 challenging. Much effort has been devoted achieving selective organic transformations . Recently, synthesis important oxazolidin-2-ones from unsaturated amines by using attracted much attention heavily studied. This Focus Review presents recent advances in this area homogenous catalysis. The cyclization that contain alkynes, alkenes, allenes with discussed, possible reaction mechanisms applications these are described.

Язык: Английский

Процитировано

88

Three-component three-bond forming cascade via palladium photoredox catalysis DOI Creative Commons
Peter Bellotti, Maximilian Koy,

Christian Gutheil

и другие.

Chemical Science, Год журнала: 2020, Номер 12(5), С. 1810 - 1817

Опубликована: Дек. 8, 2020

A highly modular radical cascade strategy based upon cyclisation/allylic substitution sequence between alkyl/aryl bromides, 1,3-dienes and nucleophiles ranging from sulfinates to amines, phenols 1,3-dicarbonyls is described (>80 examples). Palladium phosphine complexes - which merge properties of photo- cross coupling-catalysts allow forge three bonds with complete 1,4-selectivity stereocontrol, delivering value added carbocyclic heterocyclic motifs that can feature

Язык: Английский

Процитировано

85