| Literature DB >> 29931831 |
Adrian Sytniczuk1, Gwénaël Forcher1, Douglas B Grotjahn2, Karol Grela1,3.
Abstract
We report successful utilization of sequential alkene isomerization and ring-closing metathesis of dec-9-enoic acid based dienes in synthesis of macrocyclic lactones that possess a strong scent of musk. This catalytic sequence was essential to trim the chain length of starting dienes to yield macrocycles of the right size. Dec-9-enoic acid is conveniently obtainable from oleic esters by Ru-catalysed ethenolysis.Entities:
Keywords: biomass; isomerization; macrocyclization; metathesis; musk
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Year: 2018 PMID: 29931831 DOI: 10.1002/chem.201800728
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236