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Enantioselective Synthesis of (+)-Coerulescine by a Phase-Transfer Catalytic Allylation of Diphenylmethyl tert-Butyl α-(2-Nitrophenyl)Malonate : Enantioselective Synthesis of (+)-Coerulescine by a Phase-Transfer Catalytic Allylation of Diphenylmethyl tert-Butyl alpha-(2-Nitrophenyl)Malonate

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dc.contributor.authorLee, Sangki-
dc.contributor.authorYang, Jewon-
dc.contributor.authorYang, Sehun-
dc.contributor.authorLee, Geumwoo-
dc.contributor.authorOh, Daehyun-
dc.contributor.authorHa, Min Woo-
dc.contributor.authorHong, Suckchang-
dc.contributor.authorPark, Hyeung-geun-
dc.date.accessioned2023-07-10T07:08:05Z-
dc.date.available2023-07-10T07:08:05Z-
dc.date.created2020-12-15-
dc.date.created2020-12-15-
dc.date.issued2020-11-12-
dc.identifier.citationFrontiers in Chemistry, Vol.8, p. 577371-
dc.identifier.issn2296-2646-
dc.identifier.urihttps://hdl.handle.net/10371/194991-
dc.description.abstractA 7-step enantioselective synthetic method for preparing (S)(+)-coerulescine is reported through the use of diphenylmethyl tert-butyl alpha-(2-nitrophenyl)malonate (16% overall yield, >99% ee). Allylation is the key step under phase-transfer catalytic conditions (86% ee). This synthetic method can be used as a practical route for the synthesis of various derivatives of (S)(+)-coerulescine for analyzing its structure-activity relationships against its biological activities.-
dc.language영어-
dc.publisherFrontiers Media S.A.-
dc.titleEnantioselective Synthesis of (+)-Coerulescine by a Phase-Transfer Catalytic Allylation of Diphenylmethyl tert-Butyl α-(2-Nitrophenyl)Malonate-
dc.title.alternativeEnantioselective Synthesis of (+)-Coerulescine by a Phase-Transfer Catalytic Allylation of Diphenylmethyl tert-Butyl alpha-(2-Nitrophenyl)Malonate-
dc.typeArticle-
dc.identifier.doi10.3389/fchem.2020.577371-
dc.citation.journaltitleFrontiers in Chemistry-
dc.identifier.wosid000592425400001-
dc.identifier.scopusid2-s2.0-85096759101-
dc.citation.startpage577371-
dc.citation.volume8-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.contributor.affiliatedAuthorPark, Hyeung-geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusOXINDOLES-
dc.subject.keywordPlusPHALARINE-
dc.subject.keywordAuthorcoerulescine-
dc.subject.keywordAuthorenantioselective-
dc.subject.keywordAuthorsynthesis-
dc.subject.keywordAuthorphase-transfer catalysis-
dc.subject.keywordAuthoralkylation-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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