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- W2114085692 abstract "Abstract The stereoselective synthesis of (–)‐(5 R ,6 S )‐ erythro ‐6‐acetoxy‐5‐hexadecanolide, the major component of a mosquito oviposition attractant pheromone, and its enantiomer are reported. The synthesis was completed over seven steps in 28 % overall yield by using Sharpless asymmetric epoxidation and ZrCl 4 ‐catalyzed cyclic acetal formation as the key steps. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)" @default.
- W2114085692 created "2016-06-24" @default.
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- W2114085692 date "2009-03-30" @default.
- W2114085692 modified "2023-09-23" @default.
- W2114085692 title "A Facile Synthesis of Both Enantiomers of 6‐Acetoxy‐5‐hexadecanolide, a Major Component of Mosquito Oviposition Attractant Pheromones" @default.
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- W2114085692 doi "https://doi.org/10.1002/ejoc.200801134" @default.
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