Synthetic Studies toward Potent Cytotoxic Agent Amphidinolide B : Synthesis of the Entire C14-C26 Moiety of the Top Half
Regioselective hydroboration of a 4-methyl-2-alkene, oxidation of the resulting mixture of isomeric alcohols, and finally diastereoselective reduction of the ketone are the key steps in the stereoselective synthesis of C19-C26 fragment of amphidinolide B which was coupled with the C14-C18 fragment l...
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| Veröffentlicht in: | Chemistry letters 1997-06, Vol.26 (6), p.563-564 |
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| container_end_page | 564 |
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| container_issue | 6 |
| container_start_page | 563 |
| container_title | Chemistry letters |
| container_volume | 26 |
| creator | Chakraborty, Tushar K Thippeswamy, Devasamudram Suresh, Vayalakkada R Jayaprakash, Sarva |
| description | Regioselective hydroboration of a 4-methyl-2-alkene, oxidation of the resulting mixture of isomeric alcohols, and finally diastereoselective reduction of the ketone are the key steps in the stereoselective synthesis of C19-C26 fragment of amphidinolide B which was coupled with the C14-C18 fragment leading to the first synthesis of the entire C14-C26 moiety of this important molecule. |
| doi_str_mv | 10.1246/cl.1997.563 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0366-7022 |
| ispartof | Chemistry letters, 1997-06, Vol.26 (6), p.563-564 |
| issn | 0366-7022 1348-0715 |
| language | eng |
| recordid | cdi_crossref_primary_10_1246_cl_1997_563 |
| source | Oxford University Press Journals All Titles (1996-Current) |
| title | Synthetic Studies toward Potent Cytotoxic Agent Amphidinolide B : Synthesis of the Entire C14-C26 Moiety of the Top Half |
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