116102-44-4

Upstream product

• 79-01-6 Trichloroethylene 
• 2362-61-0 trans-2-Phenylcyclohexanol 
• 98919-68-7 (1R,2S)-trans-2-phenylcyclohexanol 

Downstream Products

• 130121-48-1 (+/-)-1-(trans-2-phenylcyclohexyloxy)-2-iodoethyne 
• 157358-04-8 Trimethyl-((1R,2S)-2-phenyl-cyclohexyloxyethynyl)-silane 
• 185540-97-0 Dimethyl-phenyl-[(E)-2-((1R,2S)-2-phenyl-cyclohexyloxy)-vinyl]-silane 
• 183172-53-4 (2aR,3R,6S,7S,7aS,7bR)-7-(Dimethyl-phenyl-silanyl)-2-oxo-6-((1R,2S)-2-phenyl-cyclohexyloxy)-hexahydro-1,4,5-trioxa-4a-aza-cyclopenta[cd]indene-3-carboxylic acid isopropyl ester 
• 197570-68-6 (E,E)-1,4-bis<(1R,2S)-(2-phenylcyclohexyloxy)>-1,3-butadiene 
• 133188-81-5 C₂₀H₂₀O 
• 133188-83-7 [(1R,2S)-2-(4,4-Dimethyl-pent-1-ynyloxy)-cyclohexyl]-benzene 
• 133188-79-1 ((1R,2S)-2-Hept-1-ynyloxy-cyclohexyl)-benzene 
• 133188-80-4 ((1S,2R)-2-But-1-ynyloxy-cyclohexyl)-benzene 

Relevant academic research and scientific papers

Application of the Sonogashira coupling reaction to the stereoselective synthesis of chiral 1,3-dienol ethers

Sonogashira couplings of 2-iodo enol ethers or ynol ethers provide enynes which undergo semihydrogenation to afford 4-alkyl-1,3-dienol ethers. (1Z, 3E), (1E, 3Z) and (1Z, 3Z)-4-alkyl-1,3-dienol ethers are accessible using this strategy.

A convenient synthesis of hexacarbonyldicobalt complexes of chiral (non-racemic) terminal alkoxyacetylenes

The hexacarbonyldicobalt complexes of chiral (non-racemic) unsubstituted terminal alkoxyacetylenes have been synthesized for the first time by a novel procedure that involves one-pot transformation of a chiral alcohol to the corresponding trimethylsilylat

The Resolution of Racemic Hydroperoxides: The Preparation of Optically Pure Hydroperoxide Natural Products

We report the resolution of unsaturated hydroperoxide enantiomers by liquid chromatography of diastereomeric derivatives.This method allows the nonenzymatic preparation of optically pure allylic or dienylic hydroperoxide natural products.