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pubmed-article:18811204pubmed:abstractTextMintlactone 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.lld:pubmed
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pubmed-article:18811204pubmed:authorpubmed-author:SridharSSlld:pubmed
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pubmed-article:18811204pubmed:articleTitleA synthesis of (-)-mintlactone.lld:pubmed
pubmed-article:18811204pubmed:affiliationDivision of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, 21 Nanyang Link, Nanyang Technological University, Singapore 637371. roderick@ntu.edu.sglld:pubmed
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