Synthesis of the two enantiomeric forms of 5-hexadecanolide proposed pheromone component from Vespa orientalis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. The pheromone of the queen of the Oriental hornet, Vespa orientalis
2. Synthesis of optically active .delta.-n-hexadecalactone, the proposed pheromone from Vespa orientalis
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4. Synthesis of Enantiomers of 1,2-Heptanediol
5. CI.—A synthesis of certain higher aliphatic compounds. Part III. A variation of the keto-acid synthesis, constituting an improved method for the extension of normal carbon chains
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1. Asymmetric syntheses of the lactone core of tetrahydrolipstatin and tetrahydroesterastin and of the oriental hornet Vespa Orientalis pheromone;Russian Journal of Organic Chemistry;2015-06
2. (5S)-5-hydroxy-3-methylidenehexanoate as key intermediate in synthesis of tetrahydrolipstatin and pheromone of oriental hornet Vespa Orientalis;Russian Journal of Organic Chemistry;2014-11
3. Asymmetric routes to pentadec-1-en-4-ol: application to the syntheses of aculeatins F and epi-F, (R)- and (S)-5-hexadecanolide and a formal synthesis of solenopsin;Tetrahedron: Asymmetry;2013-03
4. Enantioselective synthesis of α-benzyloxy-ω-alkenals: application to the synthesis of (+)-exo-brevicomin, (+)-iso-exo-brevicomin, and (−)-isolaurepan;Tetrahedron: Asymmetry;2007-07
5. The Synthesis of Insect Pheromones, 1979-1989;Total Synthesis of Natural Products;2007-02-20
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