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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/106398
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dc.titleSynthesis and structural studies of (2-oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acids
dc.contributor.authorDolzhenko, A.V.
dc.contributor.authorKolotova, N.V.
dc.contributor.authorKozminykh, V.O.
dc.contributor.authorChui, W.-K.
dc.contributor.authorHeng, P.W.S.
dc.contributor.authorKhrustalev, V.N.
dc.date.accessioned2014-10-29T01:59:18Z
dc.date.available2014-10-29T01:59:18Z
dc.date.issued2004-01-01
dc.identifier.citationDolzhenko, A.V.,Kolotova, N.V.,Kozminykh, V.O.,Chui, W.-K.,Heng, P.W.S.,Khrustalev, V.N. (2004-01-01). Synthesis and structural studies of (2-oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acids. Heterocycles 63 (1) : 55-62. ScholarBank@NUS Repository.
dc.identifier.issn03855414
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106398
dc.description.abstract(2-Oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acids (4a-c, 9a-c) were prepared from 2-aminopyridines by acylation with maleic or citraconic anhydrides and followed by Michael addition. Formation of 3-methyl substituted derivatives (9a-c) from citraconic anhydride was found to be regioselective. The molecular conformations of the products in the solution and in the crystal form were discussed based on 1H NMR spectral and X-Ray data.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.sourcetitleHeterocycles
dc.description.volume63
dc.description.issue1
dc.description.page55-62
dc.description.codenHTCYA
dc.identifier.isiutNOT_IN_WOS
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