99266-93-0

Upstream product

• 99383-46-7 (E)-1-Cyclohexyl-4-iodo-but-3-en-2-one 
• 23860-35-7 cyclohexylacetic acid chloride 
• 99222-87-4 (E)-4-Chloro-1-cyclohexyl-but-3-en-2-one 

Downstream Products

• 99223-04-8 (1R,4R,5S)-4-((E)-(S)-1-Cyclohexylmethyl-3-iodo-allyloxy)-6,6-dimethyl-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 99266-97-4 (1R,4R,5S)-4-((E)-(R)-1-Cyclohexylmethyl-3-iodo-allyloxy)-6,6-dimethyl-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 99223-13-9 (E)-(R)-1-Cyclohexyl-4-iodo-but-3-en-2-ol 

Relevant academic research and scientific papers

A HIGHLY EFFICIENT SYNTHESIS OF OPTICALLY PURE γ-IODO ALLYLIC ALCOHOLS AND THEIR CONVERSION INTO VARIOUS OPTICALLY ACTIVE ALLYLIC ALCOHOLS

Kinetic resolution of γ-iodo allylic alcohols 1 by the Sharpless asymmetric epoxidation reaction proceeds with very large rate differences for the two enantiomers, thus providing a highly efficient method for preparation of optically pure 1.The alcohols 1

3-Substituted iodo alkenyl compounds and methods for preparing same

Compounds of the formula: SPC1 Where R is hydrogen, methyl or ethyl; R' is hydrogen, a saturated hydrocarbon chain containing from 1 to about 9 carbon atoms, pentene, hexene, cyclohexyl, or benzyl X is hydrogen, pyranoxy, OR" where R" is a hydrocarbon chain containing from 1 to about 5 carbon atoms or benzyl, EQU1 where R"' is a hydrocarbon chain containing from 1 to about 8 carbon atoms or benzyl, or EQU2 where R1 and R2 are each a hydrocarbon chain containing from 1 to about 5 carbon atoms, and n is an integer from 0 to 5 These compounds are key intermediates in the production of prostaglandins and exhibit antibacterial properties.