Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/103108
Title: | A synthesis of 5-hydroxysedamine using hydroformylation | Authors: | Bates, Roderick Wayland Nur Filza Mohamed Aslam Tang, Chi H. Simon, Oliver |
Keywords: | Science::Chemistry::Organic chemistry::Organic synthesis | Issue Date: | 2014 | Source: | Bates, R. W., Nur Filza Mohamed Aslam, Tang, C. H., & Simon, O. (2014). A synthesis of 5-hydroxysedamine using hydroformylation. Tetrahedron, 70(12), 2134-2140. | Journal: | Tetrahedron | Series/Report no.: | Tetrahedron | Abstract: | A synthesis of 5-hydroxysedamine, a Sedum alkaloid, has been completed using N,O-heterocycle chemistry to establish the aminoalcohol structure, hydroformylation to form the piperidine ring and diastereoselective dihydroxylation to introduce the 5-hydroxy group. | URI: | https://hdl.handle.net/10356/103108 http://hdl.handle.net/10220/24359 |
ISSN: | 0040-4020 | DOI: | 10.1016/j.tet.2014.02.001 | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2014 Elsevier Ltd. This is the author created version of a work that has been peer reviewed and accepted for publication by Tetrahedron, Elsevier Ltd. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1016/j.tet.2014.02.001]. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SPMS Journal Articles |
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File | Description | Size | Format | |
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A Synthesis of 5-Hydroxysedamine using Hydroformylation.pdf | Main article | 181.55 kB | Adobe PDF | ![]() View/Open |
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