3,4-Ethylenedioxythiophene functionalizationed with tetrathiafulvalene: Synthesis and selective esterification
| dc.contributor.author | Zhang, L. | |
| dc.contributor.author | Wu, Changzhi | |
| dc.contributor.author | Wang, C. | |
| dc.contributor.author | Zuo, H. | |
| dc.contributor.author | Shen, Y. | |
| dc.date.accessioned | 2017-06-23T03:01:52Z | |
| dc.date.available | 2017-06-23T03:01:52Z | |
| dc.date.created | 2017-06-19T03:39:30Z | |
| dc.date.issued | 2015 | |
| dc.identifier.citation | Zhang, L. and Wu, C. and Wang, C. and Zuo, H. and Shen, Y. 2015. 3,4-Ethylenedioxythiophene functionalizationed with tetrathiafulvalene: Synthesis and selective esterification. Journal of Heterocyclic Chemistry. 51 (5): pp. 1277-1281. | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11937/53921 | |
| dc.identifier.doi | 10.1002/jhet.1834 | |
| dc.description.abstract |
3,4-(Hydroxymethyl-ethylenedioxy)thiophene (4) and 3,4-(2'-hydroxypropylenedioxy)thiophene (4'') were synthesized from dimethyl 3,4-dihydroxythiophene-2,5-dicarboxylate (1), which were isomers and difficult to separate. When they were esterified with tetrathiafulvalene carried carboxylic acid group, only 3,4-(hydroxymethyl-ethylenedioxy)thiophene (4) could be esterified. No such selectivity was observed when the isomers were esterified by lauric acid and benzoic acid, respectively. | |
| dc.publisher | John Wiley & Sons | |
| dc.title | 3,4-Ethylenedioxythiophene functionalizationed with tetrathiafulvalene: Synthesis and selective esterification | |
| dc.type | Journal Article | |
| dcterms.source.volume | 51 | |
| dcterms.source.number | 5 | |
| dcterms.source.startPage | 1277 | |
| dcterms.source.endPage | 1281 | |
| dcterms.source.issn | 0022-152X | |
| dcterms.source.title | Journal of Heterocyclic Chemistry | |
| curtin.department | Department of Construction Management | |
| curtin.accessStatus | Fulltext not available |
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