Green and Benign Strategies for Synthesis of Biologically Active Compounds using Lipase as Biocatalyst
DOI:
https://doi.org/10.48165/bpas.2023.42C.1.6Keywords:
Green Approach, Lipase, Biocatalyst, Biologically ActiveAbstract
An efficient, feasible, mild, affordable, and environmentally friendly method has been developed for the synthesis of biologically active compound 3-methylene-indoline-2-one from Isatin and active methylene compounds using Lipase as a Green and Biocatalyst. Biological Processes are very important to optimization to increase and improve the efficiency of cost. In this project, Malononitrile, or Dimedone reacts with Isatin in presence of lipase. The essential features of this approach are metal-free reaction, high yield, nontoxic, and less hazardous. These reactions surpass metal-catalyzed processes because these reactions have violent reaction conditions, toxic, less yields, complex workups, and environmentally hazardous ingredients. This approach replaces hazardous chemicals with benign material during their design, manufacture, use and disposal. Designing of product is cost-effective and environmentally benign chemically products. It is completely followed to Green Approach. The entire given biologically active compound have shown biological activities such as Antiviral, Anti-HIV, Antibacterial, and Anticonvulsants.
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References
Alhamdani, M., and Hanaa Jaffer Jabbar Alkabbi (2016). Isolation and identification of lipase producing bacteria from oil contaminant soil. J Bio Agri Health, 6, 1-7.
Blakemore, P.R., (2002). The modified Julia olefination: alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds. Journal of the Chemical Society, Perkin Transactions, 1 (23), 2563-2585.
Choi, Jun-Ho, and Cheol-Min Park (2018). Three-component synthesis of quinolines
based on radical cascade visible-light photoredox catalysis. Advanced Synthesis & Catalysis, 360 (18), 3553-3562.
Fu, Weijun, Xin Han, Mei Zhu, Chen Xu, Zhiqiang Wang, Baoming Ji, Xin-Qi Hao, and Mao-Ping Song (2016). Visible-light mediated radical oxydifluoromethylation of olefinic amides for the synthesis of CF 2 H
containing heterocycles. Chemical Communications, 52 (91), 13413-13416. 5. Huang, Lu-Shan, Yi-Huan Lai, Cheng Yang, and Da-Zhen Xu (2019). Iron-catalyzed one pot oxidation/Knoevenagel condensation reaction using air as an oxidant. Applied Organometallic Chemistry, 33 (6), e4910. 6. Kishore, J. P., Z. Chopdia Manojkumar, and T. M. Raghunath (2011). Lipase biodiversity. Indian J Sci Technol, 4, 971-82.
Lakhdar S, Westermaier M, Terrier F, Goumont R, Boubaker T, Ofial AR, Mayr H (2006) Nucleophilic reactivities of indoles. J Org Chem, 71, 9088–9095
Maercker, Adalbert (2004). The wittig reaction. Organic reactions, 14: 270-490. 9. McMurry, John E (1989). Carbonyl-coupling reactions using low-valent titanium. Chemical Reviews, 89 (7): 1513-1524. 10. Mol, J. C (2004). Catalytic Metathesis of Unsaturated Fatty Acid Esters and Oils. Topics in Catalysis, 27.
Revathi, Lekkala, Lekkala Ravindar, Wan Yin Fang, K. P. Rakesh, and Hua-Li Qin (2018). Visible light-induced C− H bond functionalization: a critical review. Advanced Synthesis & Catalysis, 360 (24), 4652-4698.
Sadrameli, S. M (2015). Thermal/catalytic cracking of hydrocarbons for the production of olefins: A state-of-the-art review I: Thermal cracking review, Fuel, 140, 102-115.
Sharma V, Pradeep K, Devender P (2010) Biological importance of the indole nucleus in recent years: a comprehensive review.
Journal of Heterocyclic Chemistry, 47(3), 491 – 502.
Tan, Zhi-Yu, Ke-Xin Wu, Lu-Shan Huang, Run-Shi Wu, Zheng-Yu Du, and Da-Zhen Xu (2020). Iron-catalyzed cross dehydrogenative coupling of indolin-2-ones with active methylenes for direct carbon–
carbon double bond formation. Green Chemistry, 22 (2), 332-335.
Van Staden, L. Frances, David Gravestock, and David J. Ager (2002). New developments in the Peterson olefination reaction. Chemical Society Reviews, 31 (3): 195- 200.
Verma, S. and Kanti Prakash Sharma (2014). Isolation, identification and characterization of lipase producing microorganisms from environment. Asian J Pharm Clin Res, 7(4), 219-222.
Yang, Hui, Chao Tian, Dongsheng Qiu, Haitao Tian, Guanghui An, and Guangming Li (2019). Organic photoredox catalytic decarboxylative cross-coupling of gem difluoroalkenes with unactivated carboxylic acids. Organic Chemistry Frontiers, 6 (14), 2365-2370.
Yue, Fuyang, Jianyang Dong, Yuxiu Liu, and Qingmin Wang (2021). Visible-light mediated alkenylation of alkyl boronic acids without an external Lewis base as an activator. Organic Letters, 23 (7), 2477-2481.
Yue, Fuyang, Jianyang Dong, Yuxiu Liu, and Qingmin Wang (2021). Visible-Light Mediated C–I Difluoroallylation with an α Aminoalkyl Radical as a Mediator. Organic Letters, 23 (18), 7306-7310.
Zhu, Mei, Weijun Fu, Weisi Guo, Yunfei Tian, Zhiqiang Wang, and Baoming Ji (2019). Visible-light-induced radical trifluoromethylthiolation of N-(o cyanobiaryl) acrylamides. Organic & Biomolecular Chemistry, 17, (13): 3374-3380.