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An Expedient Synthesis of Linden Ether

Academic Article
Publication Date:
2014
abstract:
We here describe a comprehensive study on the preparation of the intensive flavor 3,9-epoxy-p-mentha-1,4(8)-diene (1). Key steps of the presented synthesis are the selective addition of MeLi to the keto-ester 7, the regioselective cyclization of the obtained triol to give the ethers 4 and 8 and the selective dehydration of ether 4 through the use of POCl3 and pyridine. It is worth noting that the presented synthesis represents the first expedient and reliable entry to ether 1. Being present in linden honey, 1 is also known as linden ether and it has been regarded as a potential marker for the authentication of the linden honey origin. Therefore, ether 1 can be used as a useful reference standard for the analysis of the natural flavors, as we demonstrated by means of its identification in a sample of unifloral linden honey.
Iris type:
01.01 Articolo in rivista
Keywords:
Linden ether; p-Menthane monoterpenes; Dehydration; Stereoselective synthesis; Honey; Lime tree; Authentication
List of contributors:
Cominetti, ALESSANDRA AZZURRA; Serra, Stefano
Authors of the University:
SERRA STEFANO
Handle:
https://iris.cnr.it/handle/20.500.14243/228344
Published in:
NATURAL PRODUCT COMMUNICATIONS
Journal
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http://www.scopus.com/inward/record.url?eid=2-s2.0-84895487157&partnerID=q2rCbXpz
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