138258-88-5

Upstream product

• 145827-23-2 4-<(benzyloxy)methyl>cyclohexene 
• 138008-16-9 ((1S,2S,5R)-5-Benzyloxymethyl-2-chloro-cyclohexyloxy)-trimethyl-silane 
• 72581-32-9 cyclohex-3-enylmethanol 
• 100-39-0 benzyl bromide 
• 138124-71-7 t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane 

Downstream Products

• 138008-10-3 (1R,2R,5S)-2-Chloro-5-hydroxymethyl-cyclohexanol 
• 137946-43-1 trans-3-<(benzyloxy)methyl>-1-cyclohexanol 
• 138124-71-7 t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane 
• 137946-42-0 trans-4-(benzyloxymethyl)cyclohexanol 

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