138230-39-4

Upstream product

• 67-56-1 methanol 
• 91108-45-1 c-3,4-epoxy-r-1-cyclohexanemethanol 
• 19914-91-1 (1RS,4RS,5RS)-4-bromo-6-oxabicyclo<3.2.1>octan-7-one 
• 137946-44-2 ((1R,2R,5R)-5-Benzyloxymethyl-2-chloro-cyclohexyloxy)-trimethyl-silane 
• 137946-37-3 c-5-<(benzyloxy)methyl>-t-2-chloro-r-1-cyclohexanol 
• 137946-34-0 c-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane 
• 145827-23-2 4-<(benzyloxy)methyl>cyclohexene 
• 138008-18-1 t-4-bromo-c-3-hydroxy-r-1-cyclohexanemethanol 
• 138008-17-0 t-4-bromo-3-hydroxy-r-1-cyclohexanecarboxylic acid 
• 138124-72-8 c-4-<(benzyloxy)methyl>-t-2-methoxyy-r-1-cyclohexanol 
• 138124-73-9 methyl c-4-hydroxy-t-3-methoxy-r-1-cyclohexanecarboxylate 

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