The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol
The total syntheses of the polyhydroxylated macrolactone (+)-aspicilin and a diastereoisomer have been achieved via a concise route, starting from the spatially desymmetrized (R′,R′,R,S)-2,3-butanediacetal-protected butane tetrol 13. The key steps include a regioselective silyl protection of 13 and...
| Hlavní autoři: | , , |
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| Médium: | Journal article |
| Jazyk: | English |
| Vydáno: |
2001
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| _version_ | 1826297056391593984 |
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| author | Dixon, D Foster, A Ley, S |
| author_facet | Dixon, D Foster, A Ley, S |
| author_sort | Dixon, D |
| collection | OXFORD |
| description | The total syntheses of the polyhydroxylated macrolactone (+)-aspicilin and a diastereoisomer have been achieved via a concise route, starting from the spatially desymmetrized (R′,R′,R,S)-2,3-butanediacetal-protected butane tetrol 13. The key steps include a regioselective silyl protection of 13 and a stereoselective Lewis acid mediated addition of allyltributylstannane to the equatorially disposed aldehyde of 4. Macrocyclization is achieved using ring closing metathesis, after which selective hydrogenation and protecting group removal yields the natural product. |
| first_indexed | 2024-03-07T04:25:48Z |
| format | Journal article |
| id | oxford-uuid:cc9290bc-4691-461d-ba7f-87fc75371186 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T04:25:48Z |
| publishDate | 2001 |
| record_format | dspace |
| spelling | oxford-uuid:cc9290bc-4691-461d-ba7f-87fc753711862022-03-27T07:22:54ZThe total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocolJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cc9290bc-4691-461d-ba7f-87fc75371186EnglishSymplectic Elements at Oxford2001Dixon, DFoster, ALey, SThe total syntheses of the polyhydroxylated macrolactone (+)-aspicilin and a diastereoisomer have been achieved via a concise route, starting from the spatially desymmetrized (R′,R′,R,S)-2,3-butanediacetal-protected butane tetrol 13. The key steps include a regioselective silyl protection of 13 and a stereoselective Lewis acid mediated addition of allyltributylstannane to the equatorially disposed aldehyde of 4. Macrocyclization is achieved using ring closing metathesis, after which selective hydrogenation and protecting group removal yields the natural product. |
| spellingShingle | Dixon, D Foster, A Ley, S The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title_full | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title_fullStr | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title_full_unstemmed | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title_short | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol |
| title_sort | total synthesis of aspicilin using 2 3 butane diacetal protected butane tetrols via a chiral memory protocol |
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