Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/103107| Title: | A synthesis of cyanolide A by intramolecular oxa-Michael addition | Authors: | Bates, Roderick Wayland Lek, Tee Guan |
Keywords: | Science::Chemistry::Organic chemistry::Organic synthesis | Issue Date: | 2014 | Source: | Bates, R. W., & Lek, T. G. (2014). A synthesis of cyanolide A by intramolecular oxa-Michael addition. Synthesis, 46(13), 1731-1738. | Journal: | Synthesis | Series/Report no.: | Synthesis | Abstract: | A synthesis of cyanolide A, a diolide natural product, has been achieved using a diastereoselective Barbier reaction, early-stage glycosylation, and intramolecular oxa-Michael addition to form the THP ring. | URI: | https://hdl.handle.net/10356/103107 http://hdl.handle.net/10220/24360 |
ISSN: | 0039-7881 | DOI: | 10.1055/s-0033-1341153 | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2014 Georg Thieme Verlag KG. This is the author created version of a work that has been peer reviewed and accepted for publication by Synthesis, Georg Thieme Verlag KG. 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/10.1055/s-0033-1341153]. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
| Appears in Collections: | SPMS Journal Articles |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| A Synthesis of Cyanolide A by Intramolecular oxa-Michael Addition.pdf | Main article | 519.54 kB | Adobe PDF |  View/Open |
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