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E-7-Tetradecene-l-ol acetate

Figure 2. Separation of (Z)- and (E)-7-tetradecen-l-ol acetate (Z E7-14 Ac) and (Z)- and (E)-9-tetradecen-l-ol acetates (Z E9-14 Ac) on four different stationary phases on capillary columns. The OV-1 and Carbowax 20M (CW-20M) are coated on fused silica and the SP-2340 and p-chlorocholesteryl cinnamate on... Figure 2. Separation of (Z)- and (E)-7-tetradecen-l-ol acetate (Z E7-14 Ac) and (Z)- and (E)-9-tetradecen-l-ol acetates (Z E9-14 Ac) on four different stationary phases on capillary columns. The OV-1 and Carbowax 20M (CW-20M) are coated on fused silica and the SP-2340 and p-chlorocholesteryl cinnamate on...
Hayashi and Midorikawa have since found that the dimethyldithiocarbamate group of the products obtained above can be reductively cleaved in high yield by either lithium in ethylamine or sodium in liquid ammonia. Consequently, di- and trisubstituted olefins are readily prepared in this way. The method was used successfully for synthesis of several rianr-alkenol sex pheromones of insects, as formulated for the synthesis of E-7-tetradecene-l-ol acetate (8) in high overall yield. [Pg.12]

Tetrachlorobenzyne, 523, 524 Tetrachloroethylene, 413 Tetracyanoethylene, 271, 567-568 Tetracyclines, 109 Tetracyclone, 489, 490, 548, 577 9,11-Tetradecadien-l-yl acetate, 546 E-7-Tetradecene-l-ol acetate, 12 1,2,4,5-Tetraenes, 146 Tetraethylammonium bromide, 568-569 Tctraethylammonium chloride, 480 Tetraethylammonium cyanide, 569... [Pg.382]


See also in sourсe #XX -- [ Pg.12 ]




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Tetradecenal

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