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dc.contributor.author이학준-
dc.date.accessioned2021-05-17T05:25:17Z-
dc.date.available2021-05-17T05:25:17Z-
dc.date.issued2000-01-
dc.identifier.citationHETEROCYCLES, v. 53, no. 1en_US
dc.identifier.issn0385-5414-
dc.identifier.urihttps://www.researchgate.net/publication/244778640_An_Efficient_Synthesis_of_-cis-2Amino6-hydroxy-9-4'-hydroxyethyl-2'-cyclopenten-1'-ylpurine-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/162147-
dc.description.abstractThe synthesis of a carbovir analogue, (+/-)-cis-2-amino-6-hydroxy-9-[4'-hydroxyethyl-2'-cyclopenten-1'-yl]purine (2) was achieved from 2,5-norbornadiene (3) in six steps and 31% overall yield. This route involves a Meinwald rearrangement, one-pot operation (acid-hydrolysis and subsequent sodium borohydride reduction), and a Pd(0)-catalyzed coupling reaction.en_US
dc.language.isoen_USen_US
dc.publisherHeterocyclesen_US
dc.titleAn Efficient Synthesis of (±)-cis-2-Amino-6-hydroxy-9-[4-hydroxyethyl-2-cyclopenten-1-yl]purineen_US
dc.typeArticleen_US
dc.identifier.doi10.3987/COM-99-8740-
dc.relation.journalHETEROCYCLES-
dc.contributor.googleauthorKim, Won-
dc.contributor.googleauthorKim, Hyangdung-
dc.contributor.googleauthorRhee, Hakjune-
dc.relation.code2009203639-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E]-
dc.sector.departmentDEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING-
dc.identifier.pidhrhee-


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