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Zinc-Catalyzed Transacetalization of N, O -Acetals into N, N -Acetals with Benzotriazoles, Indazoles, and Azides

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dc.contributor.authorShin, Sang Ik-
dc.contributor.authorNguyen, Nguyen H.-
dc.contributor.authorIm, Jangbin-
dc.contributor.authorShin, Seunghoon-
dc.date.accessioned2022-07-07T00:32:59Z-
dc.date.available2022-07-07T00:32:59Z-
dc.date.created2021-07-14-
dc.date.issued2021-03-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/142233-
dc.description.abstractN , O -Acetals obtained from beta-oxidation of ynamides underwent transacetalization with benzotriazoles, leading to N , N -acetals. The Zn(OTf) (2) efficiently catalyzed the process, and the reaction is further accelerated in hexafluoroisopropanol, providing a single N1-regiosiomer. The transacetalization conditions developed could be extended to other N-donors, such as 1 H -indazole and TMSN (3) to afford the corresponding N , N -acetals.-
dc.language영어-
dc.language.isoen-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleZinc-Catalyzed Transacetalization of N, O -Acetals into N, N -Acetals with Benzotriazoles, Indazoles, and Azides-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.identifier.doi10.1055/s-0040-1707161-
dc.identifier.scopusid2-s2.0-85088589059-
dc.identifier.wosid000624909700014-
dc.identifier.bibliographicCitationSYNLETT, v.32, no.05, pp.521 - 524-
dc.relation.isPartOfSYNLETT-
dc.citation.titleSYNLETT-
dc.citation.volume32-
dc.citation.number05-
dc.citation.startPage521-
dc.citation.endPage524-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusazide-
dc.subject.keywordPlusbenzotriazole derivative-
dc.subject.keywordPlusindazole derivative-
dc.subject.keywordPlusn,n acetal derivative-
dc.subject.keywordPlusn,o acetal derivative-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPluszinc-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluscatalysis-
dc.subject.keywordPluschemical analysis-
dc.subject.keywordPluschemical modification-
dc.subject.keywordPluschemical reaction-
dc.subject.keywordPluschemical structure-
dc.subject.keywordPlusconcentration (parameter)-
dc.subject.keywordPlusoxidation-
dc.subject.keywordPlusprocess optimization-
dc.subject.keywordPlustemperature measurement-
dc.subject.keywordPlustransacetalization-
dc.subject.keywordAuthorZn catalysis-
dc.subject.keywordAuthortransacetalization-
dc.subject.keywordAuthorN-
dc.subject.keywordAuthorN-
dc.subject.keywordAuthor-acetal-
dc.subject.keywordAuthorynamide-
dc.subject.keywordAuthorbenzotriazole-
dc.identifier.urlhttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0040-1707161-
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