mintlactone has been researched along with allenolic-acid* in 1 studies
1 other study(ies) available for mintlactone and allenolic-acid
Article | Year |
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A synthesis of (-)-mintlactone.
Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction. Topics: Cyclization; Lactones; Naphthalenes; Stereoisomerism; Terpenes; Tin Compounds | 2008 |