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dc.contributor.author남길수-
dc.date.accessioned2024-01-21T03:04:52Z-
dc.date.available2024-01-21T03:04:52Z-
dc.date.created2021-09-06-
dc.date.issued2006-05-
dc.identifier.issn1229-4160-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/135537-
dc.description.abstractThe convenient stereospecific synthesis of the isosteric phosphono analogue of N-acetylglucosamine was described.Especially the α analogue of N-acetyl-D-glucosamine 1-phosphoric acid 1 has been synthesized starting from N-acetyl-D-glucosamine through the following reaction: Stereoselective radical α-1-C-allylation of 1-chloro-N-acetyl-D-glucosamine,catalytic double bond isomerization, Lemieux-Johnson oxidation, addition reaction of dialkylphosphonates, radicaldehydroxylation, and removal of protecting group. Final compound was fully characterized by NMR (1H, 13C, 19F and 31P) andHRMS experiments.-
dc.publisher한국키틴키토산학회-
dc.titleAn Efficient Stereospecific Synthesis of 1-α-C-glycosylphosphonic Acid-
dc.typeArticle-
dc.description.journalClass2-
dc.identifier.bibliographicCitationJournal of Chitin and Chitosan, v.11, no.1, pp.28 - 33-
dc.citation.titleJournal of Chitin and Chitosan-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage28-
dc.citation.endPage33-
dc.description.journalRegisteredClasskci-
dc.description.journalRegisteredClassother-
dc.identifier.kciidART001179447-
dc.subject.keywordAuthorisosteric phosphono analogue-
dc.subject.keywordAuthorα-C-glucopyranosylmethanephosphate-
dc.subject.keywordAuthorstereoselective synthesi-
dc.subject.keywordAuthorN-Acetyl-1-α-D-α-D-glucose-1-phosphate-
dc.subject.keywordAuthorisosteric phosphono analogue-
dc.subject.keywordAuthorα-C-glucopyranosylmethanephosphate-
dc.subject.keywordAuthorstereoselective synthesi-
dc.subject.keywordAuthorN-Acetyl-1-α-D-α-D-glucose-1-phosphate-
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