160537-96-2

Upstream product

• 141074-07-9 7-isopropyl-4,8-dimethyl-1-oxaspiro<5.5>undec-3-en-2-one 
• 160537-94-0 (2Z)-4-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3-methyl-2-butenoic acid 
• 7291-87-4 2-isopropyl-3-methyl-2-cyclohexen-1-one 
• 51318-62-8 ethyl (E)-4-bromo-3-methyl-2-butenoate 
• 160537-95-1 (2Z)-4-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3-methyl-2-butenol 

Downstream Products

• 160636-90-8 (2Z,4E,6Z)-ethyl 8-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3,7-dimethyl-2,4,6-octatrienoate 
• 160636-89-5 (2E,4E,6Z)-ethyl 8-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3,7-dimethyl-2,4,6-octatrienoate 
• 141074-12-6 (2E,4E,6E)-ethyl 8-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3,7-dimethyl-2,4,6-octatrienoate 
• 141194-93-6 (2Z,4E,6E)-ethyl 8-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3,7-dimethyl-2,4,6-octatrienoate 
• 141074-11-5 (2E,4E)-4-(2'-isopropyl-3'-methyl-2'-cyclohexen-1'-ylidene)-3-methyl-2-butenal 

Relevant academic research and scientific papers

A Conformationally Defined 6-s-trans-Retinoic Acid Isomer: Synthesis, Chemopreventive Activity, and Toxicity

A conformationally defined retinoic acid analog (1) which contains a dimethylene bridge to maintain the 6-s-trans orientation for two terminal double bonds in the polyene chain was synthesized.A Reformatsky reaction was utilized to extend the polyene chai