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Recent advances in the synthesis and applications of furocoumarin derivatives 被引量:1
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作者 Chaoyue Chen Zheng-Bin Tang Zhichang Liu 《Chinese Chemical Letters》 SCIE CAS CSCD 2023年第9期119-133,共15页
Furocoumarins are an important class of heterocyclic compounds with a fused tricyclic structure of coumarin and furan rings.They are commonly found in bioactive natural products and have a diverse range of biological ... Furocoumarins are an important class of heterocyclic compounds with a fused tricyclic structure of coumarin and furan rings.They are commonly found in bioactive natural products and have a diverse range of biological and pharmaceutical properties,including cytotoxicity,photosensitivity,insecticidal,antibacterial,and antifungal activity,among others.The elegant linear/angular tricyclic skeleton and superior pharmacological properties,make them ideal for building and developing advanced biological scaffolds for biomedical applications.As a result,the family of furocoumarins has been the focus of intensive research,and lots of encouraging progress have been achieved in recent years.This review summarizes the most recent methods reported for the synthesis of the furocoumarin derivative family,along with their applications in medicinal chemistry covering from 2018 to 2022. 展开更多
关键词 FUROCOUMARIN COUMARIN FURAN SYNTHESIS Pharmaceutical activity Applications
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<sup>13</sup>C-NMR Data from Coumarins from Moraceae Family 被引量:1
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作者 Raphael F. Luz Ivo J. C. Vieira +1 位作者 Raimundo Braz-Filho Vinicius F. Moreira 《American Journal of Analytical Chemistry》 2015年第11期851-866,共16页
Species from Moraceae family stand out in popular medicine and phytotherapy, have been for example used as expectorants, bronchodilators, anthelmintics and treatment of skin diseases, such as vitiligo, due to the pres... Species from Moraceae family stand out in popular medicine and phytotherapy, have been for example used as expectorants, bronchodilators, anthelmintics and treatment of skin diseases, such as vitiligo, due to the presence of compounds with proven biological activity, as the coumarins. Coumarins are lactones with 1,2-benzopyrone basic structure, and are widely distributed in the plant kingdom, both in free form, and in glycosylated form. This work reports a literature review, describing the data of 13C NMR from 53 coumarins isolated from the family Moraceae, and data comparison between genera who presented photochemical studies, in order to contribute to the chemotaxonomy of this family. 展开更多
关键词 MORACEAE COUMARIN FUROCOUMARIN Pyranocoumarin NMR Spectral Data
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A Novel Method for One-pot Synthesis of Furo[3,2-c]coumarin Derivatives from 4-Hydroxycoumarin and Arylglyoxal under Microwave Irradiation 被引量:1
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作者 陈志卫 毕建豪 苏为科 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第8期1845-1850,共6页
A novel one-pot synthesis of furo[3,2-c]coumarins has been developed from readily available starting materials 4-hydroxycoumarin and arylglyoxal. This method is simple, rapid and good yielding.
关键词 furocoumarins 4-HYDROXYCOUMARIN arylglyoxal microwave irradiation one-pot synthesis
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Synthesis and Photooxygenation of Furo[3,2-c]coumarin Derivatives as Antibacterial and DNA Intercalating Agent
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作者 Al-Sehemi,Abdullah G. EI-Gogary,Sameh R. 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第2期316-320,共5页
Syntheses of 2,3-dimethyl-4H-furo[3,2-c]coumarin and 3-phenyl-4H-furo[3,2-c]coumarin as angular furocou- marins were carried out through Williamson reaction of 4-hydroxycoumarin with a-haloketones followed by cycli- z... Syntheses of 2,3-dimethyl-4H-furo[3,2-c]coumarin and 3-phenyl-4H-furo[3,2-c]coumarin as angular furocou- marins were carried out through Williamson reaction of 4-hydroxycoumarin with a-haloketones followed by cycli- zation. Photooxygenation of the synthesized furocoumarin derivatives was performed and the photoproducts were isolated and characterized. The affinity of 2,3-dimethyl-4H-furo[3,2-c]coumarin towards DNA and the antibacterial activity were evaluated and compared with 8-methoxypsoralen (8-MOP). 展开更多
关键词 furocoumarins PSORALENS PHOTOOXYGENATION antibacterial activity and DNA
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