Abstract
AbstractThe synthesis of the four stereoisomers of 6,10,13‐trimethyl‐1‐tetradecanol (1a), the male‐produced aggregation pheromone of the predatory stink bug Stiretrus anchorago, was achieved by starting from (R)‐citronellol (2a), methyl (R)‐ or (S)‐3‐hydroxy‐2‐methylpropanoate (10) and 4‐chloro‐1‐butanol (12a).
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