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https://hdl.handle.net/10356/154863| Title: | Synthesis of fasicularin | Authors: | Kaga, Atsushi Tnay, Ya Lin Chiba, Shunsuke |
Keywords: | Science::Chemistry | Issue Date: | 2016 | Source: | Kaga, A., Tnay, Y. L. & Chiba, S. (2016). Synthesis of fasicularin. Organic Letters, 18(14), 3506-3508. https://dx.doi.org/10.1021/acs.orglett.6b01669 | Project: | RG4/13 | Journal: | Organic Letters | Abstract: | The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis. | URI: | https://hdl.handle.net/10356/154863 | ISSN: | 1523-7060 | DOI: | 10.1021/acs.orglett.6b01669 | Schools: | School of Physical and Mathematical Sciences | Rights: | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.6b01669. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
| Appears in Collections: | SPMS Journal Articles |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| manuscript_rev_deposit.pdf | 524.84 kB | Adobe PDF |  View/Open |
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