Recent Developments of Iron-Catalyzed Directed C–H Activation/C–C Bond Formation Reactions

2016 ◽  
pp. 161-174
Author(s):  
Rui Shang
Keyword(s):  
Bond Formation ◽  
Recent Developments ◽  
Bond Formation Reactions

Recent Developments in the Synthesis of Cinnoline Derivatives

2019 ◽  
Vol 16 (6) ◽  
pp. 578-588 ◽  
Author(s):  
Kamal Usef Sadek ◽  
Ramadan Ahmed Mekheimer ◽  
Mohamed Abd-Elmonem
Keyword(s):  
Reaction Mechanisms ◽  
Biological Activities ◽  
Bond Formation ◽  
Pharmaceutical Chemistry ◽  
Recent Developments ◽  
Synthetic Routes ◽  
Anti Inflammatory ◽  
Arenediazonium Salts ◽  
Metal Catalyzed ◽  
Bond Formation Reactions

Crinnolines can serve as unique and versatile class of heterocycles especially in fields related to synthetic and pharmaceutical chemistry owing to their potent biological activities. They possess diversity of pharmaceutical activities as anticancer, antibacterial, anti-inflammatory, anti-allergic as well as anti-hypertensive activities. Since the first synthesis of cinnoline by Richter (1883) numerous protocols for their synthesis have been developed utilizing arenediazonium salts, aryl hydrazines and arylhydhydrazones precursors. Recently metal catalyzed C-C and C-N bond formation reactions have emerged as efficient tools for synthesis of cinnoline derivatives. This review aims to focus on the recent synthetic routes used for the synthesis of cinnoline derivatives. An effort has been carried out to provide an overview of practical methods for preparing cinnolines. Furthermore the reaction mechanisms have been described in brief.

Recent Advances on C-Se Bond-forming Reactions at Low and Room Temperature

2020 ◽  
Vol 23 (28) ◽  
pp. 3206-3225 ◽  
Author(s):  
Amol D. Sonawane ◽  
Mamoru Koketsu
Keyword(s):  
Room Temperature ◽  
Bond Formation ◽  
Bond Forming ◽  
Material Chemistry ◽  
Recent Advances ◽  
Bond Forming Reactions ◽  
Bond Formation Reactions

: Over the last decades, many methods have been reported for the synthesis of selenium- heterocyclic scaffolds because of their interesting reactivities and applications in the medicinal as well as in the material chemistry. This review describes the recent numerous useful methodologies on C-Se bond formation reactions which were basically carried out at low and room temperature.

Synthesis of Drugs and Biorelevant N-heterocycles Employing Recent Advances in C-N Bond Formation

2020 ◽  
Vol 24 (20) ◽  
pp. 2293-2340
Author(s):  
Firdoos Ahmad Sofi ◽  
Prasad V. Bharatam
Keyword(s):  
Kinase Inhibitors ◽  
Bond Formation ◽  
Comprehensive Review ◽  
Biologically Relevant ◽  
Lead Compounds ◽  
Heterocyclic Molecules ◽  
The Past ◽  
Anti Cancer ◽  
Modern Methods ◽  
Bond Formation Reactions

C-N bond formation is a particularly important step in the generation of many biologically relevant heterocyclic molecules. Several methods have been reported for this purpose over the past few decades. Well-known named reactions like Ullmann-Goldberg coupling, Buchwald-Hartwig coupling and Chan-Lam coupling are associated with the C-N bond formation reactions. Several reviews covering this topic have already been published. However, no comprehensive review covering the synthesis of drugs/ lead compounds using the C-N bond formation reactions was reported. In this review, we cover many modern methods of the C-N bond formation reactions, with special emphasis on metal-free and green chemistry methods. We also report specific strategies adopted for the synthesis of drugs, which involve the C-N bond formation reactions. Examples include anti-cancer, antidepressant, anti-inflammatory, anti-atherosclerotic, anti-histaminic, antibiotics, antibacterial, anti-rheumatic, antiepileptic and anti-diabetic agents. Many recently developed lead compounds generated using the C-N bond formation reactions are also covered in this review. Examples include MAP kinase inhibitors, TRKs inhibitors, Polo-like Kinase inhibitors and MPS1 inhibitors.

Folding of peptides and proteins: role of disulfide bonds, recent developments

2013 ◽  
Vol 4 (6) ◽  
pp. 597-604 ◽  
Author(s):  
Yuji Hidaka ◽  
Shigeru Shimamoto
Keyword(s):  
Protein Folding ◽  
Disulfide Bonds ◽  
Bond Formation ◽  
Difficult Problem ◽  
Chemical Methods ◽  
Mutant Proteins ◽  
Folding Intermediates ◽  
Peptide Chemistry ◽  
Recent Developments

AbstractDisulfide-containing proteins are ideal models for studies of protein folding as the folding intermediates can be observed, trapped, and separated by HPLC during the folding reaction. However, regulating or analyzing the structures of folding intermediates of peptides and proteins continues to be a difficult problem. Recently, the development of several techniques in peptide chemistry and biotechnology has resulted in the availability of some powerful tools for studying protein folding in the context of the structural analysis of native, mutant proteins, and folding intermediates. In this review, recent developments in the field of disulfide-coupled peptide and protein folding are discussed, from the viewpoint of chemical and biotechnological methods, such as analytical methods for the detection of disulfide pairings, chemical methods for disulfide bond formation between the defined Cys residues, and applications of diselenide bonds for the regulation of disulfide-coupled peptide and protein folding.

Bismuth(iii)dichalcogenones as highly active catalysts in multiple C–C bond formation reactions

2016 ◽  
Vol 45 (12) ◽  
pp. 5196-5209 ◽  
Author(s):  
Katam Srinivas ◽  
Arruri Sathyanarayana ◽  
Chatla Naga Babu ◽  
Ganesan Prabusankar
Keyword(s):  
Bond Formation ◽  
Structural Motifs ◽  
Highly Active ◽  
Bond Formation Reactions

Thirteen new bismuth(iii) dichalcogenone derivatives with diversified structural motifs were successfully isolated and used as potential catalysts for the synthesis of triaryl- or triheteroarylmethanes.

Zirconium Catalyzed or Mediated Regioselective C–C Bond Formation Reactions of α,β-Unsaturated Acetals

1994 ◽  
Vol 23 (2) ◽  
pp. 259-262 ◽  
Author(s):  
Tamotsu Takahashi ◽  
Denis Y. Kondakov ◽  
Noriyuki Suzuki
Keyword(s):  
Bond Formation ◽  
Bond Formation Reactions
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