The Synthesis and the Absolute Configuration of Phoracantholide I and J; The Defensive Secretion of the Eucarypt Longicorn,Phoracantha synonyma
- 1 February 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 47 (2) , 389-393
- https://doi.org/10.1080/00021369.1983.10865622
Abstract
Both enantiomers of phoracantholide I and J were synthesized from a chiral starting material obtainable via yeast reduction, and the absolute configurations of the natural materials were determined by GLC studies using a chiral stationary phase.This publication has 4 references indexed in Scilit:
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- Cyclization catalyzed by palladium(0). Initial studies and macrolide formationJournal of the American Chemical Society, 1980
- Synthese von zwei natürlich vorkommenden Lactonen mit 10gliedrigen Ringen: (±)‐Phoracantholid J und IHelvetica Chimica Acta, 1978
- The chemistry of the metasternal gland secretion of the eucalypt longicorn Phoracantha synonyma (Coleoptera : Cerambycidae)Australian Journal of Chemistry, 1976