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ChemInform Abstract: Pheromone Synthesis. Part 177. Synthesis of the Enantiomers of 2- Methyl-4-heptanol and 2-Methyl-4-octanol, the Pheromone Components of the West Indian Sugarcane Borer.

โœ Scribed by M. TAKENAKA; H. TAKIKAWA; K. MORI


Publisher
John Wiley and Sons
Year
2010
Weight
27 KB
Volume
28
Category
Article
ISSN
0931-7597

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๐Ÿ“œ SIMILAR VOLUMES


Pheromone Synthesis, CLXXVII. Synthesis
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## Abstract Both the enantiomers of 2โ€methylโ€4โ€heptanol (1) and 2โ€methylโ€4โ€octanol (2), the components of the maleโ€produced aggregation pheromone of the West Indian sugarcane borer (__Metamasius hemipterus__), were synthesized by starting from the enantiomers of leucine.

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## Abstract Both the enantiomers of rhynchophorol [(__E__)โ€6โ€methylโ€2โ€heptenโ€4โ€ol (1)], the maleโ€produced aggregation pheromone of the American palm weevil (__Rhynchophorus palmarum__), have been synthesized by reducing their precursors, (__R__)โ€ and (__S__)โ€6โ€methylโ€2โ€heptynโ€4โ€ol (2), which have b

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Pheromone Synthesis. Part 194. Synthesis of the Enantiomers of (Z)-21-Methyl-8-pentatriacontene, the Major Component of the Female-Produced Contact Sex Pheromone of the Yellow-Spotted Longicorn Beetle, Psacothea hilaris. -The (R)-enantiomer of the title compound (I) is synthesized starting from (S)-