ChemInform Abstract: A Novel Approach for C-C, C-N, and C-O Bond Formation Reactions: A Facile Synthesis of Benzophenazine, Quinoxaline, and Phenoxazine Derivatives via Ring Opening of Benzoxepines.

ChemInform ◽  
2014 ◽  
Vol 45 (26) ◽  
pp. no-no
Author(s):  
Bhimapaka China Raju ◽  
Kasagani Veera Prasad ◽  
Gannerla Saidachary ◽  
Balasubramanian Sridhar
2020 ◽  
Vol 23 (28) ◽  
pp. 3206-3225 ◽  
Author(s):  
Amol D. Sonawane ◽  
Mamoru Koketsu

: 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.


2020 ◽  
Vol 24 (20) ◽  
pp. 2293-2340
Author(s):  
Firdoos Ahmad Sofi ◽  
Prasad V. Bharatam

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.


ChemInform ◽  
2013 ◽  
Vol 44 (18) ◽  
pp. no-no
Author(s):  
Honglai Jiang ◽  
Aijun Lin ◽  
Chengjian Zhu ◽  
Yixiang Cheng

2016 ◽  
Vol 45 (12) ◽  
pp. 5196-5209 ◽  
Author(s):  
Katam Srinivas ◽  
Arruri Sathyanarayana ◽  
Chatla Naga Babu ◽  
Ganesan Prabusankar

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.


2018 ◽  
Vol 361 (1) ◽  
pp. 214-218 ◽  
Author(s):  
Zi Yang ◽  
Lianghua Jie ◽  
Zhenyu Yao ◽  
Zhimin Yang ◽  
Xiuling Cui
Keyword(s):  

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