Synthesis and Biological Properties of Coumarin Analogue: A Brief Review

被引:9
|
作者
Chaudhary, Diksha [1 ]
Bedi, Pooja [1 ]
Santra, Soumava [1 ]
Pramanik, Tanay [2 ]
机构
[1] Lovely Profess Univ, Fac Technol & Sci, Sch Chem Engn & Phys Sci, Dept Chem, POB 144411, Phagwara, India
[2] Univ Engn & Management, Dept Chem, Act Area 3,B-5, Kolkata 700160, India
关键词
Coumarin; pechmann condensation; phenols; beta-keto ester; biological properties; heterocycles; ONE-POT SYNTHESIS; SOLVENT-FREE SYNTHESIS; VON-PECHMANN REACTION; ANTIMICROBIAL ACTIVITY; EFFICIENT CATALYST; RECYCLABLE CATALYST; CRYSTAL-STRUCTURES; ACID CATALYST; IONIC LIQUID; DERIVATIVES;
D O I
10.2174/1570178618666210202152452
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
One of the most prominent aromatic organic chemical compound is Coumarin having formula C9H6O2 which is widely known for its benefits in drug industry. Colourless crystalline solid having sweet scent is coumarin's physical identity. It serves various purposes such as in synthesis of medicines, laser dyes, perfumes and many more. Having enormous usages, it becomes important to synthesize such compound so various reactions were performed in order to obtain coumarins. This review explicates the preparation of coumarin by Pechmann Condensation and its biological characteristics.
引用
收藏
页码:362 / 387
页数:26
相关论文
共 50 条
  • [21] Synthesis, and Fluorescence Properties of Coumarin and Benzocoumarin Derivatives Conjugated Pyrimidine Scaffolds for Biological Imaging Applications
    Najim A. Al-Masoudi
    Niran J. Al-Salihi
    Yossra A. Marich
    Timo Markus
    Journal of Fluorescence, 2015, 25 : 1847 - 1854
  • [22] A NEW COUMARIN SYNTHESIS AND ITS UTILIZATION FOR THE SYNTHESIS OF POLYCYCLIC COUMARIN COMPOUNDS WITH ANTICARCINOGENIC PROPERTIES
    HARVEY, RG
    CORTEZ, C
    ANANTHANARAYAN, TP
    SCHMOLKA, S
    JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (17): : 3936 - 3943
  • [23] Biological correlates of psychopathy: a brief review
    Debowska, Agata
    Boduszek, Daniel
    Hyland, Philip
    Goodson, Simon
    MENTAL HEALTH REVIEW JOURNAL, 2014, 19 (02) : 110 - +
  • [24] Chemical synthesis, characterization and biological properties of a novel cyclic ADP-ribose analogue
    Wang, Pei
    Zhang, Yan
    Yang Zhen-Jun
    Zhang Liang-Ren
    Zhang Li-He
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2008, 29 (02): : 314 - 318
  • [25] Design, synthesis and biological activity of a novel Rutin analogue with improved lipid soluble properties
    Baldisserotto, Anna
    Vertuani, Silvia
    Bino, Alessia
    De Lucia, Daniela
    Lampronti, Ilaria
    Milani, Roberta
    Gambari, Roberto
    Manfredini, Stefano
    BIOORGANIC & MEDICINAL CHEMISTRY, 2015, 23 (01) : 264 - 271
  • [26] Synthesis and Biological Activity of Triterpene-Coumarin Conjugates
    Vega-Granados, Karina
    Medina-O'Donnell, Marta
    Rivas, Francisco
    Reyes-Zurita, Fernando J.
    Martinez, Antonio
    de Cienfuegos, Luis Alvarez
    Lupianez, Jose A.
    Parra, Andres
    JOURNAL OF NATURAL PRODUCTS, 2021, 84 (05): : 1587 - 1597
  • [27] Synthesis and biological activity of a fluorescent schweinfurthin analogue
    Kuder, Craig H.
    Neighbors, Jeffrey D.
    Hohl, Raymond J.
    Wiemer, David F.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (13) : 4718 - 4723
  • [28] Synthesis and Biological Properties of some New Lead Sulphonamide and Carboxamide Scaffolds Bearing Coumarin Moieties
    Eze, Cosmas Chinweike
    Ezeokonkwo, Mercy Amarachukwu
    Ezema, Benjamin Ebere
    Onoabedje, Abraham Efeturi
    Ugwu, David Izuchukwu
    MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2021, 21 (11) : 1270 - 1287
  • [29] Synthesis and biological evaluation of a beauveriolide analogue library
    Nagai, K
    Doi, T
    Sekiguchi, T
    Namatame, I
    Sunazuka, T
    Tomoda, H
    Omura, S
    Takahashi, T
    JOURNAL OF COMBINATORIAL CHEMISTRY, 2006, 8 (01): : 103 - 109
  • [30] Synthesis and biological activity of human calcitonin analogue
    Yu, C
    Zhou, GM
    Li, BL
    Wu, XF
    Cui, DF
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 1999, 31 (05) : 553 - 557