3685-24-3

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 91108-45-1 c-3,4-epoxy-r-1-cyclohexanemethanol 
• 64-17-5 ethanol 
• 3618-04-0 trans-4-hydroxy-cyclohexane carboxylic acid ethyl ester 
• 138008-18-1 t-4-bromo-c-3-hydroxy-r-1-cyclohexanemethanol 
• 99-96-7 4-hydroxy-benzoic acid 
• 3685-26-5 trans-4-hydroxycyclohexanecarboxylic acid 
• 138008-17-0 t-4-bromo-3-hydroxy-r-1-cyclohexanecarboxylic acid 
• 19914-91-1 (1RS,4RS,5RS)-4-bromo-6-oxabicyclo<3.2.1>octan-7-one 

Downstream Products

• 881648-69-7 cis-1-chloromethyl-cyclohexanol-⁽⁴⁾ 
• 1217682-91-1 cis-4-(toluene-sulfonyl-⁽⁴⁾-oxy)-1-(toluene-sulfonyl-⁽⁴⁾-oxymethyl)-cyclohexane 
• 73856-82-3 cis-(1-mesyloxymethyl-4-hydroxy)cyclohexane 
• 33073-73-3 cis-4-Hydroxycyclohexylcarbinolphosphat 

Relevant academic research and scientific papers

Regiochemical Control of the Ring-Opening of 1,2-Epoxides by Means of Chelating Processes. 2. Synthesis and Reactions of the cis- and trans-Oxides of 4-cyclohexene, 3-Cyclohexenemethanol, and Methyl 3-Cyclohexenecarboxylate

The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ring-opening by various nucleophiles are described.The results of the ring-openings of the trans-epoxides 2b-d can be rationalized by combining stereoelectro