Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/7183
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dc.contributor.authorManolov, Stanimir P.-
dc.contributor.authorAtanasova, Stoyanka N.-
dc.contributor.authorGhate, Manjunath-
dc.contributor.authorIvanov, Iliyan I.-
dc.date.accessioned2016-10-28T09:37:11Z-
dc.date.available2016-10-28T09:37:11Z-
dc.date.issued2015-
dc.identifier.urihttp://hdl.handle.net/123456789/7183-
dc.descriptionIndian journal of Chemistry, 54B; 2015 pp 1301-1320en_US
dc.description.abstract1,2,3,4-Tetrahydroisoquinolines are an important class of synthetic and natural compounds, which display a broad range of medicinal activities. The 1,2,3,4-tetrahydroisoquinoline system has attracted attention not only because of its biological activities, but also due to its presence as a basic framework in many naturally occurring products and drugs. Their skeletons are unique among the Amaryllidaceae alkaloids and they have long been alluring targets for synthetic chemists as witnessed by a number of articles dealing with biogenesis, isolation, characterization and synthesis. The alkaloid cherylline is an optically active naturally occurring, 4-phenyl-1,2,3,4-tetrahydroisoquinoline alkaloid, isolated from Crinum powelli, Amaryllidaceae plant. There are many ways for cherylline synthesis. In this short review is described the different methods for synthesis of the alkaloid cheryllineen_US
dc.publisherNISCAIRen_US
dc.relation.ispartofseriesIPFP0228;-
dc.subjectCheryllineen_US
dc.subjectCrinumen_US
dc.subjectSynthesisen_US
dc.subjectAmaryllidaceae alkaloidsen_US
dc.subjectIPFP0228en_US
dc.titleAdvances in contemporary research a brief review of cherylline synthesisen_US
dc.typeArticleen_US
Appears in Collections:Faculty Papers

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