159826-46-7

Upstream product

• 20536-36-1 neryl chloride 
• 5042-53-5 1-(phenylsulfanyl)acetone 
• 3879-26-3 (Z)-nerylacetone 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 159826-47-8 ethyl 3,7,11-trimethyl-4-(phenylthio)dodeca-2Z,6Z,10-trienoate 
• 159826-53-6 tert-butyl 3,7,11-trimethyl-4-(phenylthio)dodeca-2Z,6Z,10-trienoate 
• 159826-54-7 tert-butyl 3,7,11-trimethyl-4-(phenylthio)dodeca-2E,6Z,10-trienoate 
• 159826-50-3 3,7,11-trimethyl-4-(phenylthio)dodeca-2E,6Z,10-trien-1-ol 
• 159826-49-0 3,7,11-trimethyl-4-(phenylthio)dodeca-2Z,6Z,10-trien-1-ol 
• 16106-95-9 (2Z,6Z)-farnesol 
• 13927-47-4 (3E,5Z)-6,10-dimethyl-3,5,9-undecatrien-2-one 
• 159826-51-4 methyl 3,7,11-trimethyl-4-(phenylthio)dodeca-2Z,6Z,10-trienoate 

Relevant academic research and scientific papers

Z-Stereoselective Peterson olefination of ketones

A highly-stereoselective method (90percent of the Z-isomer) was developed for the Peterson olefination of ketones with nerylacetone (1) as an example.The method is based on the introduction of a PhS group, which is removed after completion of the reaction, at the ketone C(3) atom. - Keywords: olefination of ketones, stereoselective synthesis, Peterson reaction, 2Z- and 2E-4-phenylthiofarnesoles and 2Z- and 2E-4-phenylthiofarnesoates

New access to pseudo-ionones and pseudo-iso-methyl ionones from geranyl derivatives

Pseudo-ionones and pseudo-iso-methyl ionones, precursors of fragrant derivatives were obtained from geranyl chloride, an industrially available starting material.