2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone
The title diacetonide, C13H20O7, readily available in quantity from D-tagatose, is likely to be a useful carbohydrate starting material. The current structure analysis resolves any ambiguities arising from the synthetic route over the configuration at the new chiral centre and the size of the lacton...
| Main Authors: | , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2004
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| _version_ | 1797090402980855808 |
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| author | Shallard-Brown, H Harding, C Watkin, D Soengas, R Skytte, U Fleet, G |
| author_facet | Shallard-Brown, H Harding, C Watkin, D Soengas, R Skytte, U Fleet, G |
| author_sort | Shallard-Brown, H |
| collection | OXFORD |
| description | The title diacetonide, C13H20O7, readily available in quantity from D-tagatose, is likely to be a useful carbohydrate starting material. The current structure analysis resolves any ambiguities arising from the synthetic route over the configuration at the new chiral centre and the size of the lactone ring, but otherwise shows no unusual features. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved. |
| first_indexed | 2024-03-07T03:18:05Z |
| format | Journal article |
| id | oxford-uuid:b67dc4fc-3219-4ac0-8eae-70c7feb257ef |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:18:05Z |
| publishDate | 2004 |
| record_format | dspace |
| spelling | oxford-uuid:b67dc4fc-3219-4ac0-8eae-70c7feb257ef2022-03-27T04:41:21Z2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactoneJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b67dc4fc-3219-4ac0-8eae-70c7feb257efEnglishSymplectic Elements at Oxford2004Shallard-Brown, HHarding, CWatkin, DSoengas, RSkytte, UFleet, GThe title diacetonide, C13H20O7, readily available in quantity from D-tagatose, is likely to be a useful carbohydrate starting material. The current structure analysis resolves any ambiguities arising from the synthetic route over the configuration at the new chiral centre and the size of the lactone ring, but otherwise shows no unusual features. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved. |
| spellingShingle | Shallard-Brown, H Harding, C Watkin, D Soengas, R Skytte, U Fleet, G 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title | 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title_full | 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title_fullStr | 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title_full_unstemmed | 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title_short | 2,3 : 5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone |
| title_sort | 2 3 5 6 di o isopropylidene 2 c hydroxy methyl d talono 1 4 lactone |
| work_keys_str_mv | AT shallardbrownh 2356dioisopropylidene2chydroxymethyldtalono14lactone AT hardingc 2356dioisopropylidene2chydroxymethyldtalono14lactone AT watkind 2356dioisopropylidene2chydroxymethyldtalono14lactone AT soengasr 2356dioisopropylidene2chydroxymethyldtalono14lactone AT skytteu 2356dioisopropylidene2chydroxymethyldtalono14lactone AT fleetg 2356dioisopropylidene2chydroxymethyldtalono14lactone |