Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/86029
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Russell, R.A. | - |
dc.contributor.author | Collin, G.J. | - |
dc.contributor.author | Gee, P.S. | - |
dc.contributor.author | Warrener, R.N. | - |
dc.date.issued | 1983 | - |
dc.identifier.citation | Journal of the Chemical Society, Chemical Communications, 1983; 1983(18):994-995 | - |
dc.identifier.issn | 0022-4936 | - |
dc.identifier.uri | http://hdl.handle.net/2440/86029 | - |
dc.description.abstract | 5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct of buta-1,3-diene and p-benzoquinone, is selectively deacetylated (Cs2CO3 in tetrahydrofuran or K2CO3 in dimethyl sulphoxide) to intermediates suitable for use in chiral anthracycline synthesis. | - |
dc.description.statementofresponsibility | Richard A. Russell, Geoffrey J. Collin, Paul S. Gee and Ronald N. Warrener | - |
dc.language.iso | en | - |
dc.publisher | Royal Society of Chemistry | - |
dc.rights | Copyright status unknown | - |
dc.source.uri | http://dx.doi.org/10.1039/c39830000994 | - |
dc.title | An economical and versatile synthesis of 5,8-dialkoxy-2-acetyl-3,4-dihydronaphthalenes: key precursors for the synthesis of chiral anthracyclines | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1039/c39830000994 | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest 7 Chemistry publications |
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