112497-26-4

Upstream product

• 133216-88-3 (+/-)-1-cyclohexyl-3-(trimethylsilyl)-2-propynol 
• 1066-54-2 trimethylsilylacetylene 
• 2043-61-0 cyclohexanecarbaldehyde 

Downstream Products

• 112497-36-6 (2E,4Z)-5-Cyclohexyl-penta-2,4-dien-1-ol 
• 112497-35-5 (Z)-(2R,3R)-5-Cyclohexyl-3-trimethylsilanyl-pent-4-ene-1,2-diol 
• 112497-37-7 (2Z,4Z)-5-Cyclohexyl-penta-2,4-dienoic acid isopropyl ester 
• 112497-30-0 (Z)-(2R,3R)-5-Cyclohexyl-2-hydroxy-3-trimethylsilanyl-pent-4-enoic acid isopropyl ester 
• 112497-28-6 ((E)-1-Cyclohexyl-3-trimethylsilanyl-allyloxy)-acetic acid isopropyl ester 
• 112497-32-2 (Z)-(2R,3R)-5-Cyclohexyl-2-(tetrahydro-pyran-2-yloxy)-3-trimethylsilanyl-pent-4-enoic acid isopropyl ester 
• 1022099-96-2 C₁₈H₃₈OSi₂ 
• 154808-45-4 (R)-(-)-3-cyclohexyl-3-(4-fluorophenyl)-3-hydroxypropyl toluenesulfonate 
• 154808-46-5 (S)-(+)-3-cyclohexyl-3-(4-fluorophenyl)-3-hydroxypropyl toluenesulfonate 
• 154808-42-1 (4R,5S)-(-)-4-cyclohexyl-4-(4-fluorophenyl)-5-(trimethylsilyl)methyl-1,3-dioxolan-2-one 
• 154904-34-4 (4S,5R)-(+)-4-cyclohexyl-4-(4-fluorophenyl)-5-(trimethylsilyl)methyl-1,3-dioxolan-2-one 
• 154808-41-0 (1R,2S,3S)-(-)-1-cyclohexyl-2,3-epoxy-1-(4-fluorophenyl)-3-(trimethylsilyl)-1-propanol 
• 154904-33-3 (1S,2R,3R)-(+)-1-cyclohexyl-2,3-epoxy-1-(4-fluorophenyl)-3-(trimethylsilyl)-1-propanol 
• 154808-51-2 (1R,2S)-(+)-1-cyclohexyl-1-(4-fluorophenyl)-3-(trimethylsilyl)propane-1,2-diol 

Relevant academic research and scientific papers

Hexafluoroisopropanol as a unique solvent for stereoselective lododesilylation of vinylsilanes

Stereoselective preparation of iodoalkenes from vinylsilanes is described. 1,1,1,3,3,3-Hexafluoroisopropanol serves as a unique solvent that ensures high yields and stereoselectivities in the iododesilylation of a variety of functionalized substrates.

Anticholinergic agents. 4. Stereocontrolled synthesis of fluorinated acetylcholine antagonists; syntheses of the two 1-cyclohexyl-1-(4-fluorophenyl)-3-piperidyl-1-propanols and their methiodides.

Four new putative muscarinic antagonists, (R)-(-)- and (S)-(+)-1-cyclohexyl-1-(4-fluorophenyl)-3-piperidyl-1-propanol and their methiodides, have been synthesised. Absolute configurations have been assigned on the basis of the anticipated chirality of the

A regiodefined synthesis of α-trimethylsilyl ketones catalyzed by rhodium(I) hydride complex

Regiodefined synthesis of α-trimethylsilyl ketones is attained by one of three different routes: isomerization of β-trimethylsilyl allyl alcohols (route A), isomerization of β'-trimethylsilyl allyl alcohols (route B), and dehydrogenation of β-trimethylsil

STEREOSELECTIVE SYNTHESIS OF (2E,4Z)-DIEN-1-OLS; KEY INTERMEDIATES FOR SYNTHESIS OF SEX PHEROMONES OF SILK WORM AND OF GRAPE VINE MOTH

Two (2E,4Z)-dien-1-ols, synthetic key intermediates for the insect pheromones with a (E,Z)-diene system, were synthesized stereoselectively by using a combination of zirconium-mediated Wittig rearrangement reaction and Peterson reaction as key steps.