High-Valent Cobalt-Catalyzed C H Bond Functionalization DOI
Tatsuhiko Yoshino, Shigeki Matsunaga

Advances in organometallic chemistry, Journal Year: 2017, Volume and Issue: unknown, P. 197 - 247

Published: Jan. 1, 2017

Language: Английский

3d Transition Metals for C–H Activation DOI
Parthasarathy Gandeepan, Thomas Müller, Daniel Zell

et al.

Chemical Reviews, Journal Year: 2018, Volume and Issue: 119(4), P. 2192 - 2452

Published: Nov. 27, 2018

C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with notable applications to material crop protection, drug discovery, and pharmaceutical industries, among others. Despite major advances, the vast majority of these functionalizations required precious 4d or 5d transition metal catalysts. Given cost-effective sustainable nature earth-abundant first row metals, development less toxic, inexpensive 3d catalysts gained considerable recent momentum a significantly more environmentally-benign economically-attractive alternative. Herein, we provide comprehensive overview on until summer 2018.

Language: Английский

Citations

1970

A comprehensive overview of directing groups applied in metal-catalysed C–H functionalisation chemistry DOI Creative Commons
Carlo Sambiagio, David Schönbauer, Rémi Blieck

et al.

Chemical Society Reviews, Journal Year: 2018, Volume and Issue: 47(17), P. 6603 - 6743

Published: Jan. 1, 2018

The present review is devoted to summarizing the recent advances (2015-2017) in field of metal-catalysed group-directed C-H functionalisation. In order clearly showcase molecular diversity that can now be accessed by means directed functionalisation, whole organized following directing groups installed on a substrate. Its aim comprehensive reference work, where specific group easily found, together with transformations which have been carried out it. Hence, primary format this schemes accompanied concise explanatory text, are ordered sections according their chemical structure. feature typical substrates used, products obtained as well required reaction conditions. Importantly, each example commented respect most important positive features and drawbacks, aspects such selectivity, substrate scope, conditions, removal, greenness. targeted readership both experts functionalisation chemistry (to provide overview progress made last years) and, even more so, all organic chemists who want introduce way thinking for design straightforward, efficient step-economic synthetic routes towards molecules interest them. Accordingly, should particular also scientists from industrial R&D sector. overall goal promote application reactions outside research dedicated method development establishing it valuable archetype contemporary R&D, comparable role cross-coupling play date.

Language: Английский

Citations

1469

Weak-Coordination in C–H Bond Functionalizations Catalyzed by 3d Metals DOI
Rajib Mandal,

Bholanath Garai,

Basker Sundararaju

et al.

ACS Catalysis, Journal Year: 2022, Volume and Issue: 12(6), P. 3452 - 3506

Published: March 3, 2022

Transition-metal-catalyzed C–H bond functionalizations have had an enormous influence on organic synthesis in recent times. However, the use of low-abundance 4d and 5d metals is almost inevitable, they are high demand. This will be a cause concern, hence, it important to develop methods based 3d metals, which widely present Earth's crust. In this regard, metal catalysts or their precursors for catalysis, general, functionalizations, particular, has gained significant momentum The major development catalytic with been achieved predominantly strongly coordinating directing groups such as pyridyl, pyrimidinyl, pyrazolyl, 8-amino-quinolinyl groups. Thus, prefunctionalization substrates these necessary, contradicts step- atom-economy activation. commonly available functional aldehyde, ketone, carboxylic acid, amide, hydroxy, N-oxides loosely bind through weak-coordination. These weakly orient activate regioselectively without need preinstalled Although challenging, contemporary topic actively pursued by many researchers Through article, we provide comprehensive overview metal-catalyzed, coordinating, directing-group-enabled reported until March 2021.

Language: Английский

Citations

118

Recent advances using [Cp*Co(CO)I2] catalysts as a powerful tool for C–H functionalisation DOI

Paula G. Chirila,

Christopher J. Whiteoak

Dalton Transactions, Journal Year: 2017, Volume and Issue: 46(30), P. 9721 - 9739

Published: Jan. 1, 2017

This perspective highlights recent applications of Cp*CoIII catalysts in C–H functionalisation protocols, exemplifying both terminal couplings and heterocycle formation.

Language: Английский

Citations

129

Recent advances in the synthetic and medicinal perspective of quinolones: A review DOI

Prashant Dhiman,

Nidhi Arora, Punniyakoti T. Veeraveedu

et al.

Bioorganic Chemistry, Journal Year: 2019, Volume and Issue: 92, P. 103291 - 103291

Published: Sept. 19, 2019

Language: Английский

Citations

125

Cobalt-catalyzed C–H activation: recent progress in heterocyclic chemistry DOI
Sankuviruthiyil M. Ujwaldev, Nissy Ann Harry, Mathiyazhagan Arun Divakar

et al.

Catalysis Science & Technology, Journal Year: 2018, Volume and Issue: 8(23), P. 5983 - 6018

Published: Jan. 1, 2018

Cobalt-catalyzed C–H activation has gone through some major advancements in the past couple of decades.

Language: Английский

Citations

100

Direct Access to Cobaltacycles via C–H Activation: N-Chloroamide-Enabled Room-Temperature Synthesis of Heterocycles DOI
Xiaolong Yu,

Kehao Chen,

Shan Guo

et al.

Organic Letters, Journal Year: 2017, Volume and Issue: 19(19), P. 5348 - 5351

Published: Sept. 19, 2017

Cobaltacycle synthesis via C-H activation has been achieved for the first time, providing key mechanistic insight into cobalt catalytic chemistry. N-Chloroamides are used as a directing synthon cobalt-catalyzed room-temperature and construction of heterocycles. Alkynes coupling partners allow convenient access to isoquinolones, class synthetically pharmaceutically important compounds. The broad substrate scope enables diverse range substitution patterns be incorporated heterocyclic scaffold.

Language: Английский

Citations

99

Cp*Co(III)-Catalyzed C–H Acylmethylation of Arenes by Employing Sulfoxonium Ylides as Carbene Precursors DOI

Shuying Ji,

Kelu Yan, Bin Li

et al.

Organic Letters, Journal Year: 2018, Volume and Issue: 20(18), P. 5981 - 5984

Published: Sept. 12, 2018

A Cp*Co(III)-catalyzed C-H bond functionalization of a range arenes by employing sulfoxonium ylides as carbene precursors instead diazo compounds and other has been established. This reaction is highly efficient without any additive, possesses high step atom economies, tolerates functional groups.

Language: Английский

Citations

94

Quinolone: a versatile therapeutic compound class DOI Open Access
Phelelisiwe S. Dube, Lesetja J. Legoabe, Richard M. Beteck

et al.

Molecular Diversity, Journal Year: 2022, Volume and Issue: 27(3), P. 1501 - 1526

Published: Dec. 17, 2022

Language: Английский

Citations

50

“Alkene-to-Alkene” Difunctionalization of Enaminones for the Synthesis of Polyfunctionalized Alkenes by Transition-Metal-Free C–H and C–N Bond Transformation DOI

J. Ye,

Yunyun Liu,

Jin Luo

et al.

Organic Letters, Journal Year: 2023, Volume and Issue: 25(47), P. 8451 - 8456

Published: Nov. 16, 2023

The three-component reactions of enaminones, disulfides, and alcohols for the synthesis polyfunctionalized alkenes have been realized via C-H C-N bond transformation on enaminones. proceed in a novel "alkene-to-alkene" difunctionalization mode without using any transition metal. application alkene products divergent sulfenyl heteroaryls, including sulfenylated pyrazoles, pyrimidines, isoxazoles, simple annulation has also verified.

Language: Английский

Citations

29