A Review on Green Synthesis of Biologically Active Compounds

被引:6
作者
Kushwaha, Smriti [1 ]
Baranwal, Jyoti [1 ]
Singh, Swastika [1 ]
Jyoti, Archana [1 ]
机构
[1] Univ Allahabad, S S Khanna Girls Degree Coll, Dept Chem, Prayagraj 211001, Uttar Pradesh, India
关键词
Biologically active compounds; catalyst; green synthesis; solvents; visible light; green chemistry; SOLVENT-FREE SYNTHESIS; MICROWAVE-ASSISTED SYNTHESIS; LIGHT-MEDIATED SYNTHESIS; GAMMA-VALEROLACTONE; CATALYST-FREE; OXYGEN REDUCTION; PROPYLENE CARBONATE; ORGANIC-SYNTHESIS; ONE-POT; MULTICOMPONENT REACTIONS;
D O I
10.2174/2213346110666221213092734
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent decades, green synthesis is increasingly being employed for more environmentally friendly processes and constitutes one central theme of research and development in both academic and industrial chemistry. "Green Chemistry" refers to the design of products and processes that imply the reduction or elimination of substances that are harmful to life or the environment. Due to the benefits of green synthesis, such as reduced waste and expense, not just pharmaceutical firms but also other chemical industries have begun to take steps towards it. Green synthesis techniques include using green solvents, catalysts, and other materials. This review article illustrates the utilization of sustainable methods in the synthesis of biologically active compounds via different green methodologies, such as green solvents, green catalyst, green media, etc. We hope that this chapter will provide a quick overview of the different aspects of green chemistry.
引用
收藏
页码:174 / 195
页数:22
相关论文
共 231 条
[1]   Synthesis and Antimicrobial Activities of Some New Heterocyclic Compounds Based on 6-Chloropyridazine-3(2H)-thione [J].
Abd El-Salam, Nasser M. ;
Mostafa, Mohamed S. ;
Ahmed, Gamal A. ;
Alothman, Othman Y. .
JOURNAL OF CHEMISTRY, 2013, 2013
[2]   Reaction between isocyanides and chalcones: an effcient solvent-free synthesis of 5-hydroxy-3,5-diaryl-1,5dihydro-2H-pyrrol-2-ones [J].
Adib, Mehdi ;
Mahdavi, Mohammad ;
Noghani, Mahsa Alizadeh ;
Bijanzadeh, Hamid Reza .
TETRAHEDRON LETTERS, 2007, 48 (45) :8056-8059
[3]   Updating and further expanding GSK's solvent sustainability guide [J].
Alder, Catherine M. ;
Hayler, John D. ;
Henderson, Richard K. ;
Redman, Aniko M. ;
Shukla, Lena ;
Shuster, Leanna E. ;
Sneddon, Helen F. .
GREEN CHEMISTRY, 2016, 18 (13) :3879-3890
[4]  
Ali NAS, 2013, MINI-REV MED CHEM, V13, P1792
[5]   Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass [J].
Alonso, David Martin ;
Wettstein, Stephanie G. ;
Dumesic, James A. .
GREEN CHEMISTRY, 2013, 15 (03) :584-595
[6]  
Alonso DM, 2013, ENERG ENVIRON SCI, V6, P76, DOI [10.1039/c2ee23617f, 10.1039/C2EE23617F]
[7]   What do we know about multicomponent reactions? Mechanisms and trends for the Biginelli, Hantzsch, Mannich, Passerini and Ugi MCRs [J].
Alvim, Haline G. O. ;
da Silva Junior, Eufranio N. ;
Neto, Brenno A. D. .
RSC ADVANCES, 2014, 4 (97) :54282-54299
[8]  
Anastas P.T., 2000, GREEN CHEM SYNTHESIS, DOI [10.1021/bk-2000-0767, DOI 10.1021/BK-2000-0767]
[9]  
Anastas PT, 1998, GREEN CHEMISTRY, P1
[10]   Origins, current status, and future challenges of green chemistry [J].
Anastas, PT ;
Kirchhoff, MM .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (09) :686-694