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DC Field | Value | Language |
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dc.contributor.author | Ahmed, M. Giasuddin | - |
dc.contributor.author | Ahmed, S. Asghari | - |
dc.contributor.author | Romman, U. K. R. | - |
dc.contributor.author | Akhter, Kawsari | - |
dc.contributor.author | Halim, Md. Ershad | - |
dc.contributor.author | Naher, Shamsun | - |
dc.contributor.author | Aslam, M. | - |
dc.contributor.author | Ahmed, S. Mosaddeq | - |
dc.date.accessioned | 2021-10-31T17:04:27Z | - |
dc.date.available | 2021-10-31T17:04:27Z | - |
dc.date.issued | 2011-07 | - |
dc.identifier.issn | 1022-016X | - |
dc.identifier.uri | http://dspace.aiub.edu:8080/jspui/handle/123456789/180 | - |
dc.description.abstract | Spiro compounds 7,11-diaryl-2,4-diazaspiro[5,5]undecane-1,3,5,9-tetraones 3a-d were prepared by carrying out reactions between diarylideneacetones, (ArCH=CH)2C=O, 2a-d [Ar= 2-CH3C6H4, 4-CH3C6H4, 4-(CH3)2NC6H4 and 4-HOC6H4 respectively] and barbituric acid (1a) under refluxing condition in aqueous ethanol medium without using any catalyst. Under similar conditions the corresponding 7,11-diaryl-3-thioxo-2,4-diazaspiro[5,5]undecane-1,5,9-triones 3e-g were synthesized from the reactions of diarylideneacetones 2a, 2d and 2e [Ar= 4-ClC6H4] with 2-thiobarbituric acid (1b). The structures of the spiro compounds were established with the help of their UV, IR, 1H NMR, 13C NMR and mass spectral data and elemental analyses. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Bangladesh Chemical Society (BCS) | en_US |
dc.relation.ispartofseries | 24(2);Page 135-142 | - |
dc.subject | Spiro compounds, diarylideneacetones, barbituric acid, 2-thiobarbituric acid, Michael addition | en_US |
dc.title | A one pot synthesis of 7,11-diaryl-2,4-diazaspiro[5,5]undecane-3-oxo(or thioxo)-1,5,9-triones | en_US |
dc.type | Article | en_US |
Appears in Collections: | Publication: Journal |
Files in This Item:
File | Description | Size | Format | |
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Spiro-1 P2_JBCS_2011.docx | Summary Sheet | 3.54 MB | Microsoft Word XML | View/Open |
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