72530-35-9

Upstream product

• 88730-59-0 Methyl 6-<(2-Tetrahydropyranyl)oxy>-(Z)-hex-3-enoate 
• 38341-83-2 methyl (3Z)-6-hydroxy-3-hexenoate 
• 104178-62-3 6-<(tetrahydro-2H-pyran-2-yl)oxy>-3-hexyn-1-ol 
• 88730-60-3 (Z)-6-(tetrahydro-2H-pyran-2-yloxy)hex-3-en-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 120385-67-3 (Z)-6-(2,3-Dimethyl-1-cyclohexen-1-yl)-3-hexen-1-ol 
• 120385-63-9 2-<(Z)-6-Hydroxy-3-hexen-1-yl>-3,4-dimethyl-2-cyclohexen-1-on 
• 120385-55-9 (Z)-6-(2,3-Dimethyl-1-cyclohexen-1-yl)-3-hexensaeure 
• 120385-71-9 (1'α,6'α)-(Z)-6-(2',3'-Dimethyl-6'-methoxy-2'-cyclohexen-1'-yl)-3-hexen-1-ol 
• 120385-66-2 2,3-Dimethyl-1-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-1-cyclohexen 
• 120385-64-0 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-2-cyclohexen-1-ol 
• 120385-62-8 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-2-cyclohexen-1-on 
• 120385-69-5 (1α,2α)-3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-ol 
• 120385-65-1 3-Methoxy-1,6-dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-1-cyclohexen 
• 120385-68-4 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on 
• 120385-61-7 4-<2-(Diethylamino)ethoxy>-1,2-dimethyl-3-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-1,4-cyclohexadien 
• 120385-57-1 (1'α,6'β)-(Z)-6-(2',3'-Dimethyl-6'-methoxy-2'-cyclohexen-1'-yl)-3-hexensaeure 
• 120385-57-1 (1'α,6'α)-(Z)-6-(2',3'-Dimethyl-6'-methoxy-2'-cyclohexen-1'-yl)-3-hexensaeure 
• 120385-70-8 (3α,4β)-1,2-Dimethyl-4-methoxy-3-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-1-cyclohexen 

Relevant academic research and scientific papers

Tuning the reactivity of oxygen/sulfur by acidity of the catalyst in Prins cyclization: Oxa-versus thia-selectivity

An unprecedented oxa- versus thia-selectivity has been observed in Prins cyclization of 6-mercaptohex-3-en-1-ol with aldehydes. In the presence of a stoichiometric amount of strong Lewis or Bronsted acids, the reaction provides the hexahydro-2H-thieno[3,2

Synthesis of the Sesquiterpene (+/-)-Lemnal-5a-en-2-one

SnCl4-catalysed cyclization of the carboxylic acid 4 stereoselectively gives the tricyclus 5.This cyclization is the key reaction in the synthesis of lemnal-5a-en-2-one .As a model compound the carboxylic acid 2 was cyclized to yield 3. 2 and 4 w

Synthesis of ω-Tritiated and ω-Fluorinated Analogues of the Trail Pheromone of Subterranean Termites

A series of unsaturated ω-fluoro alcohols have been prepared stereoselectively.These simple compounds are structural analogues of the trail pheromone of termites in the genus Reticulitermes.The toxicity of these ω-fluoro alcohols to R. flavipes is maximal for the C12 alcohols, and the attractiveness of these C12 analogues increases in the order saturated alkanol -12-fluoro alcohols and a -nonfluorinated analogue were prepared to examine the catabolism of the pheromone analogues.