99222-87-4

Upstream product

• 23860-35-7 cyclohexylacetic acid chloride 
• 74-86-2 acetylene 

Downstream Products

• 99266-93-0 3-hydroxy-1-iodo-4-cyclohexyl-1-trans-butene 
• 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 
• 99223-04-8 (1R,4R,5S)-4-((E)-(S)-1-Cyclohexylmethyl-3-iodo-allyloxy)-6,6-dimethyl-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 99223-13-9 (E)-(R)-1-Cyclohexyl-4-iodo-but-3-en-2-ol 
• 99222-95-4 (E)-(S)-1-Cyclohexyl-4-iodo-but-3-en-2-ol 
• 99234-56-7 6-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(E)-(S)-3-(tert-butyl-dimethyl-silanyloxy)-4-cyclohexyl-but-1-enyl]-5-oxo-cyclopentylsulfanyl}-hexanoic acid methyl ester 
• 99234-57-8 6-[(2S,3R)-2-((E)-(S)-4-Cyclohexyl-3-hydroxy-but-1-enyl)-3-hydroxy-5-oxo-cyclopentylsulfanyl]-hexanoic acid methyl ester 
• 99223-05-9 Benzoic acid (E)-(S)-1-cyclohexylmethyl-3-iodo-allyl ester 
• 99223-03-7 tert-Butyl-((E)-(S)-1-cyclohexylmethyl-3-iodo-allyloxy)-dimethyl-silane 
• 99383-46-7 (E)-1-Cyclohexyl-4-iodo-but-3-en-2-one 

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

Synthesis of 7-thiaprostaglandin E1 congeners: Potent inhibitors of platelet aggregation

Novel 7-thiaprostaglandin E1 derivatives and congeners were synthesized by a stepwise three-component coupling process, which involves the introduction of α-side chains (thiols) and β-side chains (organocopper reagents) into (R)-4-tert-butyldim