Chemistry:Bourgeanic acid
From HandWiki
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| Names | |
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| IUPAC name
(2S,3S,4R,6R)-3-[(2S,3S,4R,6R)-3-hydroxy-2,4,6-trimethyloctanoyl]oxy-2,4,6-trimethyloctanoic acid[1]
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| Other names
(+)-bourgeanic acid
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
PubChem CID
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| Properties | |
| C22H42O5 | |
| Molar mass | 386.573 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
Bourgeanic acid is a fatty acid with the molecular formula C22H42O5.[2][3][1] Bourgeanic acid is a lichen metabolite.[3][2]
References
- ↑ 1.0 1.1 "Bourgeanic acid" (in en). Pubchem.ncbi.NLM.nih.gov. https://pubchem.ncbi.nlm.nih.gov/compound/Bourgeanic-acid#section=3D-Conformer.
- ↑ 2.0 2.1 Brodo, Irwin M.; Sharnoff, Sylvia Duran; Sharnoff, Stephen; Nature, Canadian Museum of (1 January 2001) (in en). Lichens of North America. Yale University Press. p. 247. ISBN 978-0-300-08249-4.
- ↑ 3.0 3.1 Majumdar, Krishna C.; Chattopadhyay, Shital K. (15 June 2011) (in en). Heterocycles in Natural Product Synthesis. John Wiley & Sons. p. 32. ISBN 978-3-527-63489-7.
Further reading
- Johnson, Alan Thomas (1990) (in en). Total Synthesis of (+)-bourgeanic Acid and Conformational Analysis of Its Dilactone. Oregon State University.
- Yadav, Jhillu; Rao, Tenneti; Yadav, Nagendra; Rao, Kovvuru; Reddy, Basi; Al Khazim Al Ghamdi, Ahmad (March 2012). "Chemoenzymatic Approach to the Total Synthesis of (+)-Bourgeanic Acid". Synthesis 44 (5): 788–792. doi:10.1055/s-0031-1289699.
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