Adelaide Research & Scholarship
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https://hdl.handle.net/2440/111622
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| Type: | Journal article |
| Title: | Total synthesis of the pseudopterosin aglycones |
| Author: | Newton, C. Sherburn, M. |
| Citation: | Natural Product Reports: a journal of current development in bioorganic chemistry, 2015; 32(6):865-876 |
| Publisher: | Royal Society of Chemistry |
| Issue Date: | 2015 |
| ISSN: | 0265-0568 1460-4752 |
| Statement of Responsibility: | Christopher G. Newton and Michael S. Sherburn |
| Abstract: | Covering up to 2015: The pseudopterosin natural products have been the focus of a substantial number of synthetic studies since the first members were isolated almost 30 years ago. Herein we review all total and formal syntheses of this family of glycosylated diterpenes, with an emphasis on the synthetic strategies employed |
| Keywords: | Diterpenes Glycosides Biological Products Molecular Structure Stereoisomerism |
| Rights: | This journal is © The Royal Society of Chemistry 2015 |
| DOI: | 10.1039/C5NP00008D |
| Grant ID: | ARC |
| Published version: | http://dx.doi.org/10.1039/c5np00008d |
| Appears in Collections: | Aurora harvest 8 Chemistry and Physics publications |
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