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• W2733132625 abstract "An expedient enantioselective synthetic approach for the gypsy moth sex-attractant pheromone cis-(+)-1 and trans-(+)-disparlure 2 is described employing the optimized combination of organocatalytic MacMillan’s self aldol reaction, Wittig olefination, regioselective ring opening of an epoxide and Mitsunobu esterification reactions as key steps." @default.
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• W2733132625 date "2017-08-01" @default.
• W2733132625 modified "2023-10-02" @default.
• W2733132625 title "Enantioselective total synthesis of cis -(+)- and trans -(+)-disparlure" @default.
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• W2733132625 doi "https://doi.org/10.1016/j.tetlet.2017.07.024" @default.
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