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2000
Volume 9, Issue 9
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A practical and scalable synthesis of (Z)-9-tricosene, the sex pheromone of the housefly, has been achieved by the addition of one-carbon unit from the readily available (Z)-erucic acid. The synthesis is composed of three consecutive steps, lithium aluminium hydride reduction of erucic acid, tosylation of the resulting alcohol, and copper-catalyzed Kumada- type cross-coupling of the tosylate with methylmagnesium bromide as the key step. This approach is quite straightforward and capable of scale-up synthesis.

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/content/journals/loc/10.2174/157017812803521199
2012-11-01
2025-09-30
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