Pheromone synthesis. Part 240: Cross-metathesis with Grubbs I (but not Grubbs II) catalyst for the synthesis of (R)-trogodermal (14-methyl-8-hexadecenal) to study the optical rotatory powers of compounds with a terminal sec-butyl group

被引:23
|
作者
Mori, Kenji [1 ]
机构
[1] Toyo Gosei Co Ltd, Photosensit Mat Res Ctr, Inba, Chiba 2701609, Japan
关键词
Cross-metathesis; Optical rotation; Pheromone; Trogodermal; FEMALE DERMESTID BEETLE; TROGODERMA COLEOPTERA; ABSOLUTE-CONFIGURATIONS; ACTIVE FORMS; ATTRACTANT; COMPONENTS;
D O I
10.1016/j.tet.2009.02.064
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
(R)-Trogodermal (14-methyl-8-hexadecenal), the sex pheromone of Trogoderma species of pest insects against stored products, and its (S)-isomer were synthesized by using olefin cross-metathesis between (R)- or (S)-7-methyl-1-nonene and 8-nonenyl acetate as the key step. This step was successful with Grubbs I but not With Grubbs II Catalyst. The latter caused randomization of the carbon skeleton to give a mixture of abnormal products with both longer or shorter carbon chains than the desired product. The specific rotations of 18 newly and 6 previously synthesized compounds with a terminal sec-butyl group were measured to conclude them to be [alpha](D) + 3.5 to +6.5 or -3.6 to -6.4. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:3900 / 3909
页数:10
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