Transition-metal-free synthesis of oxazoles: valuable structural fragments in drug discovery

RSC Advances ◽  
2016 ◽  
Vol 6 (95) ◽  
pp. 93016-93047 ◽  
Author(s):  
Aliya Ibrar ◽  
Imtiaz Khan ◽  
Naeem Abbas ◽  
Umar Farooq ◽  
Ajmal Khan

This review article encapsulates the recent developments in the metal-free approaches used to construct oxazole moiety.

Synlett ◽  
2018 ◽  
Vol 29 (05) ◽  
pp. 548-555 ◽  
Author(s):  
Liang-Nian He ◽  
Xiao-Fang Liu ◽  
Xiao-Ya Li ◽  
Chang Qiao

Reductive functionalization of CO2 with amines and a reductant, which combines both reduction of CO2 and C–N bond formation in one pot to produce versatile chemicals and energy-storage materials such as formamides, aminals, and methylamines that are usually derived from petroleum feedstock, would be appealing and promising. Herein, we give a brief review on recent developments in the titled CO2 chemistry by employing transition-metal-free catalysis, which can be catalogued as below according to the diversified energy content of the products, that is formamides, aminals, and methylamines being consistent with 2-, 4-, and 6-electron reduction of CO2, respectively. Notably, hierarchical reduction of CO2 with amines to afford at least two products, for example, formamides and methylamines, could be realized with the same catalyst through tuning the hydrosilane type, reaction temperature, or CO2 pressure. Finally, the opportunities and challenges of the reductive functionalization of CO2 with amines are also highlighted.1 Introduction2 2-Electron Reduction of CO2 to Formamide3 6-Electron Reduction of CO2 to Methylamine4 4-Electron Reduction of CO2 to Aminal5 Hierarchical Reduction of CO2 with Amines6 Conclusion


Synlett ◽  
2020 ◽  
Author(s):  
Lei Jiao ◽  
Fei-Yu Zhou

AbstractPyridine is an important structural motif that is prevalent in natural products, drugs, and materials. Methods that functionalize and derivatize pyridines have gained significant attention. Recently, a large number of transition-metal-free reactions have been developed. In this review, we provide a brief summary of recent advances in transition-metal-free functionalization and derivatization reactions of pyridines, categorized according to their reaction modes.1 Introduction2 Metalated Pyridines as Nucleophiles2.1 Deprotonation2.2 Halogen–Metal exchange3 Activated Pyridines as Electrophiles3.1 Asymmetric 2-Allylation by Chiral Phosphite Catalysis3.2 Activation of Pyridines by a Bifunctional Activating Group3.3 Alkylation of Pyridines by 1,2-Migration3.4 Alkylation of Pyridines by [3+2] Addition3.5 Pyridine Derivatization by Catalytic In Situ Activation Strategies3.6 Reactions via Heterocyclic Phosphonium Salts4 Radical Reactions for Pyridine Functionalization4.1 Pyridine Functionalization through Radical Addition Reactions4.2 Pyridine Functionalization through Radical–Radical Coupling Reactions5 Derivatization of Pyridines through the Formation of Meisenheimer-Type Pyridyl Anions6 Conclusion


ChemInform ◽  
2016 ◽  
Vol 47 (48) ◽  
Author(s):  
Aliya Ibrar ◽  
Imtiaz Khan ◽  
Naeem Abbas ◽  
Umar Farooq ◽  
Ajmal Khan

Synlett ◽  
2017 ◽  
Vol 28 (19) ◽  
pp. 2525-2538 ◽  
Author(s):  
James Bull ◽  
Renzo Luisi ◽  
Leonardo Degennaro

Sulfoximines are emerging as valuable new isosteres for use in medicinal chemistry, with the potential to modulate physicochemical properties. Recent developments in synthetic strategies have made the unprotected ‘free’ NH-sulfoximine group more readily available, facilitating further study. This account reviews approaches to NH-sulfoximines, with a focus on our contribution to the field. Starting from the development of catalytic strategies involving transition metals, more sustainable metal-free processes have been discovered. In particular, the use of hypervalent iodine reagents to mediate NH-transfer to sulfoxides is described, along with an assessment of the substrate scope. Furthermore, a one-pot strategy to convert sulfides directly into NH-sulfoximines is discussed, with N- and O-transfer occurring under the reaction conditions. Mechanistic evidence for the new procedures is included as well as relevant synthetic applications that further exemplify the potential of these approaches.1 Introduction2 Strategies to Form NH-Sulfoximines Involving Transition-Metal Catalysts3 Metal-Free Strategies to Prepare NH-Sulfoximines4 Mechanistic Evidence for the Direct Synthesis of NH-Sulfoximines from Sulfoxides and Sulfides5 Further Applications6 Conclusion


Synthesis ◽  
2018 ◽  
Vol 50 (11) ◽  
pp. 2131-2149 ◽  
Author(s):  
Kamal Kapoor ◽  
Parthasarathi Das ◽  
Rajni Khajuria ◽  
Sk. Rasheed ◽  
Chhavi Khajuria

Pyrido[1,2-a]benzimidazole is one of the most important azaheterocyclic compounds consisting of three fused aromatic rings. Molecules containing this core have displayed a wide range of applications in the field of medicinal chemistry. The synthesis of pyrido[1,2-a]benzimidazole and its derivatives has attracted organic chemists because of its tremendous utility in interdisciplinary branches of chemistry. In this context, this review discusses the main advances in the synthesis of pyrido[1,2-a]benzimidazoles via metal-mediated and metal-free reactions from 2000 to 2016.1 Introduction2 Synthetic Approaches to Pyrido[1,2-a]benzimidazoles2.1 Type I: Transition-Metal-Catalyzed Methods2.2 Type II: Metal-Free Approaches3 Conclusion


RSC Advances ◽  
2021 ◽  
Vol 11 (59) ◽  
pp. 37325-37353
Author(s):  
Biplob Borah ◽  
L. Raju Chowhan

Recent advances in the synthesis of quinoxalines under transition metal free conditions are summarized in this review article.


Synthesis ◽  
2017 ◽  
Vol 50 (01) ◽  
pp. 49-63 ◽  
Author(s):  
N. Lemcoff ◽  
Or Eivgi

Olefin metathesis is one of the most important methods to form carbon–carbon double bonds and has found many applications in industry and academia. The ability to initiate the reaction using external stimulus such as light, with high spatial and temporal resolution is highly advantageous and provides creative novel opportunities in organic syntheses and material sciences. This review article covers recent advances in light-activated olefin metathesis reactions from the development of novel complexes that can be initiated photochemically to recently reported applications of photoinduced olefin metathesis, as well as the bright newly emerging field of photoredox-mediated metal-free ROMP.1 Introduction2 Light-Activated Olefin Metathesis Complexes2.1 Sulfur-Chelated Hoveyda–Grubbs-Type Complexes2.2 Nitrogen-Chelated Hoveyda–Grubbs-Type Complexes2.3 Catalyst Activation with Photoacid Generators2.4 Phototuning of Active Complexes2.5 Photoactivation of Non-Grubbs-Type Olefin Metathesis Complexes3 Photoredox-Mediated Metal-Free ROMP4 Applications of Photoinduced Olefin Metathesis4.1 Chromatic Orthogonal Olefin Metathesis4.2 UV-Filter-Assisted Olefin Metathesis4.3 Photolithographic Olefin Metathesis Polymerization5 Conclusions


2021 ◽  
Author(s):  
Mohit L. Deb ◽  
B Shriya Saikia ◽  
Paran J. Borpatra ◽  
Pranjal K. Baruah

This review article focuses on the functionalization of α-C-H bond of tertiary amines via C-H activation catalyzed by iodine or its derivatives. Recently, transition metal-free C-H functionalizations in organic syntheses...


2016 ◽  
Vol 45 (5) ◽  
pp. 1273-1307 ◽  
Author(s):  
Ming Zhou ◽  
Hsing-Lin Wang ◽  
Shaojun Guo

We summarize and discuss recent developments of different-dimensional advanced carbon nanomaterial-based noble-metal-free high-efficiency oxygen reduction electrocatalysts, including heteroatom-doped, transition metal-based nanoparticle-based, and especially iron carbide (Fe3C)-based carbon nanomaterial composites.


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