Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/103938
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dc.contributor.authorNguyen, Van Vinh Ha-
dc.contributor.authorNguyen, Thi Thu Ha-
dc.contributor.authorOng, Ngoc Khanh-
dc.contributor.authorDinh, Truc Phuong-
dc.contributor.authorHo, Thanh Nhat-
dc.contributor.authorNguyen, Thanh Tung-
dc.date.accessioned2024-06-26T07:38:28Z-
dc.date.available2024-06-26T07:38:28Z-
dc.date.issued2023-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/103938-
dc.description.abstractHerein we reported a method for copper pivalate mediated, directed functionalization of ortho C-H bonds in (2- methylthio) aniline benzamides. Diaryl disulfides were used for thiolation, while successful phenoxylation was obtained with phenol as the coupling agent. Our report marks a rare example for flexible transformation of benzamide C(sp²)-H bonds into the corresponding unsymmetrical diaryl ethers and thioethers.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam journal of Chemistry;Vol.61, No.02 .- P.204-209-
dc.subjectC-H functionalizationvi_VN
dc.subjectCoppervi_VN
dc.subjectThiolationvi_VN
dc.subjectPhenolvi_VN
dc.subjectDirecting groupvi_VN
dc.titleCopper promoted, directed sulfenylation and phenoxylation of benzamide C-H bondsvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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