Please use this identifier to cite or link to this item:
http://hdl.handle.net/11189/4755| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mei, Mawonga N | - |
| dc.contributor.author | Hugo, Victor I | - |
| dc.contributor.author | Green, Ivan R | - |
| dc.date.accessioned | 2016-07-27T13:35:11Z | - |
| dc.date.available | 2016-07-27T13:35:11Z | - |
| dc.date.issued | 2011 | - |
| dc.identifier.uri | http://dx.doi.org/10.1080/00397911.2010.482039 | - |
| dc.identifier.uri | http://hdl.handle.net/11189/4755 | - |
| dc.description.abstract | A protocol has been developed for the synthesis of the linear naphthopyran 16, by the TiCl4-catalyzed isomerization of 2,5-dimethyl dioxolane 1, having a methoxy group at position 1′ and a bromine atom at position 4′ of the naphthyl precursor to favor isomerization at position 2′. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Taylor and Francis | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/3.0/za/ | en |
| dc.subject | Isomerization | en_US |
| dc.subject | Naphthopyranquinones | en_US |
| dc.subject | Naphthopyrans | en_US |
| dc.subject | Naphthyldioxolanes | en_US |
| dc.title | Model route to 5-bromo-3,4-dihydro-4- hydroxy-7,9,10-trimethoxy-1,3-dimethyl-1H- naphtho[2,3-c]pyran: A potential precursor to extended quinines | en_US |
| dc.type.patent | Article | en_US |
| Appears in Collections: | Appsc - Journal Articles (DHET subsidised) | |
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