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Asymmetric Synthesis of Novel Structural Mimics of Sulphidoleukotrienes
An asymmetric synthetic route toward a new class of structural mimics of the sulphidoleukotrienes has been developed. The key steps in the overall synthetic sequence include Sharpless asymmetric epoxidation followed by stereo- and regioselective opening of the epoxide ring.
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| Published in: | Chemistry letters 1997-01, Vol.26 (1), p.15-16 |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c371t-41db0783189b0722c6c8ddb3161a92d607961dc7b9c43fc3bfb5ab0cd35d8ffa3 |
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| cites | cdi_FETCH-LOGICAL-c371t-41db0783189b0722c6c8ddb3161a92d607961dc7b9c43fc3bfb5ab0cd35d8ffa3 |
| container_end_page | 16 |
| container_issue | 1 |
| container_start_page | 15 |
| container_title | Chemistry letters |
| container_volume | 26 |
| creator | Ovaska, Timo V Voynov, George H McNeil, Nicole Hokkanen, Joel A |
| description | An asymmetric synthetic route toward a new class of structural mimics of the sulphidoleukotrienes has been developed. The key steps in the overall synthetic sequence include Sharpless asymmetric epoxidation followed by stereo- and regioselective opening of the epoxide ring. |
| doi_str_mv | 10.1246/cl.1997.15 |
| format | article |
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| fulltext | fulltext |
| identifier | ISSN: 0366-7022 |
| ispartof | Chemistry letters, 1997-01, Vol.26 (1), p.15-16 |
| issn | 0366-7022 1348-0715 |
| language | eng |
| recordid | cdi_proquest_journals_1460871669 |
| source | Oxford Journals Online |
| title | Asymmetric Synthesis of Novel Structural Mimics of Sulphidoleukotrienes |
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