Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/61007
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dc.contributor.authorBui, Thuy Trang-
dc.contributor.authorCao, Hai Thuong-
dc.contributor.authorPham, Xuan Thao-
dc.contributor.authorDinh, Hung Mac-
dc.contributor.authorGrée, Rene-
dc.date.accessioned2021-08-11T02:46:36Z-
dc.date.available2021-08-11T02:46:36Z-
dc.date.issued2021-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/61007-
dc.description.abstractSotolon (3-hydroxy-4,5-dimethyl-2(5H)-furanone) has been synthezised both in racemic and enantioenriched forms by a short sequence involving intramolecular tandem isomerization-aldolisation and tandem izomerization/Mannich reactions as key steps. Optically active Sotolon has been obtained by using (S)-N-tert-butane sulfinimine as a chiral starting material.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam Journay of Chemistry;No.59(1) .- P.42-46-
dc.subjectSotolonvi_VN
dc.subjectIsomerization-Mannichvi_VN
dc.subjectCatalysisvi_VN
dc.subjectNickelvi_VN
dc.subjectα-aminoestervi_VN
dc.titleA New Approach for the Synthesis of Sotolon in Racemic and Enantioenriched Formsvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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