2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone
The crystal structure of the title benzyl ether, C20H 26O7, establishes the stereochemistry of the major diacetonide product from the Kiliani reaction of D-psicose. There are two independent molecules in the cell related by a pseudo-twofold screw axis. There are no suitable donors for strong hydroge...
| Main Authors: | , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2005
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| _version_ | 1826306495226052608 |
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| author | Watkin, D Parry, L Soengas, R Izumori, K Fleet, G |
| author_facet | Watkin, D Parry, L Soengas, R Izumori, K Fleet, G |
| author_sort | Watkin, D |
| collection | OXFORD |
| description | The crystal structure of the title benzyl ether, C20H 26O7, establishes the stereochemistry of the major diacetonide product from the Kiliani reaction of D-psicose. There are two independent molecules in the cell related by a pseudo-twofold screw axis. There are no suitable donors for strong hydrogen bonds: the molecules are simply in van der Waals contact. © 2005 International Union of Crystallography Printed in Great Britain - all rights reserved. |
| first_indexed | 2024-03-07T06:48:49Z |
| format | Journal article |
| id | oxford-uuid:fbcb2a98-fa37-4dc5-81f2-ba110ff41f4e |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T06:48:49Z |
| publishDate | 2005 |
| record_format | dspace |
| spelling | oxford-uuid:fbcb2a98-fa37-4dc5-81f2-ba110ff41f4e2022-03-27T13:16:22Z2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactoneJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fbcb2a98-fa37-4dc5-81f2-ba110ff41f4eEnglishSymplectic Elements at Oxford2005Watkin, DParry, LSoengas, RIzumori, KFleet, GThe crystal structure of the title benzyl ether, C20H 26O7, establishes the stereochemistry of the major diacetonide product from the Kiliani reaction of D-psicose. There are two independent molecules in the cell related by a pseudo-twofold screw axis. There are no suitable donors for strong hydrogen bonds: the molecules are simply in van der Waals contact. © 2005 International Union of Crystallography Printed in Great Britain - all rights reserved. |
| spellingShingle | Watkin, D Parry, L Soengas, R Izumori, K Fleet, G 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title | 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title_full | 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title_fullStr | 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title_full_unstemmed | 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title_short | 2-C-Benzyloxymethyl-2,3 : 5,6-di-O-isopropylidene-D-allono-1,4-lactone |
| title_sort | 2 c benzyloxymethyl 2 3 5 6 di o isopropylidene d allono 1 4 lactone |
| work_keys_str_mv | AT watkind 2cbenzyloxymethyl2356dioisopropylidenedallono14lactone AT parryl 2cbenzyloxymethyl2356dioisopropylidenedallono14lactone AT soengasr 2cbenzyloxymethyl2356dioisopropylidenedallono14lactone AT izumorik 2cbenzyloxymethyl2356dioisopropylidenedallono14lactone AT fleetg 2cbenzyloxymethyl2356dioisopropylidenedallono14lactone |