Synthesis of the enantiomers of 13‐methylheptacosane, the sex pheromone of pear psylla, Cacopsylla pyricola

An efficient and gram‐scale enantioselective synthesis of (R)‐ and (S)‐13‐methylheptacosane, the sex pheromone of pear psylla, has been developed. The key steps of the approach included Evans' chiral auxiliaries and Wittig coupling of chiral phosphonium salt with aldehyde. An efficient and gram...

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Veröffentlicht in:Chirality (New York, N.Y.) N.Y.), 2021-06, Vol.33 (6), p.274-280
Hauptverfasser: Yuan, Gucheng, Yang, Yuxiong, Liu, Jiawei, Bian, Qinghua, Wang, Min, Zhong, Jiangchun
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Sprache:eng
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Zusammenfassung:An efficient and gram‐scale enantioselective synthesis of (R)‐ and (S)‐13‐methylheptacosane, the sex pheromone of pear psylla, has been developed. The key steps of the approach included Evans' chiral auxiliaries and Wittig coupling of chiral phosphonium salt with aldehyde. An efficient and gram‐scale enantioselective synthesis of (R)‐ and (S)‐13‐methylheptacosane, the sex pheromone of pear psylla, has been developed. The key steps of the approach included Evans' chiral auxiliaries and Wittig coupling of chiral phosphonium salt with aldehyde.
ISSN:0899-0042
1520-636X
DOI:10.1002/chir.23307