Deprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxide

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dc.contributor.authorJ D Kim-
dc.contributor.authorGyoon Hee Han-
dc.contributor.authorO P Zee-
dc.contributor.authorY H Jung-
dc.date.accessioned2017-04-19T08:59:39Z-
dc.date.available2017-04-19T08:59:39Z-
dc.date.issued2003-
dc.identifier.issn0040-4039-
dc.identifier.uri10.1016/S0040-4039(02)02648-5ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6047-
dc.description.abstractCSI-NaOH procedure provided a new and mild methodology for the deprotection of benzyl and p-methoxybenzyl ethers without affecting the other functional groups under similar reaction conditions.-
dc.publisherElsevier-
dc.titleDeprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxide-
dc.title.alternativeDeprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxide-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number4-
dc.citation.endPage735-
dc.citation.startPage733-
dc.citation.volume44-
dc.contributor.affiliatedAuthorGyoon Hee Han-
dc.contributor.alternativeName김지덕-
dc.contributor.alternativeName한균희-
dc.contributor.alternativeName지옥표-
dc.contributor.alternativeName정영훈-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 44, no. 4, pp. 733-735-
dc.identifier.doi10.1016/S0040-4039(02)02648-5-
dc.description.journalClassY-
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