136667-75-9

Upstream product

• 84049-33-2 (1SR,3RS,6RS)-3-(benzyloxy)-7-oxabicyclo[4.1.0]heptane 
• 84029-18-5 (1RS,3RS,6SR)-3-(benzyloxy)-7-oxabicyclo[4.1.0]heptane 

Downstream Products

• 136667-70-4 t-5-(Benzyloxy)-t-2-(N,N-diethylamino)-r-1-cyclohexanol 
• 136667-79-3 (1β,4β,6α)-4-(Benzyloxy)-8-oxo-7-oxa-9-azabicyclo<4.3.0>nonane 
• 136667-78-2 t-2-Amino-t-5-(benzyloxy)-r-1-cyclohexanol 

Relevant academic research and scientific papers

Regiochemical control of the ring opening of aziridines by means of chelating processes. Synthesis and ring-opening reactions of cis- and trans-aziridines derived from 4-(benzyloxy)cyclohexene

The regiochemical outcome of the ring opening of aziridines bearing a polar remote functionality was verified in a conformationally semirigid bicyclic system in which the polar functionality (OBn) is in an homoallylic relationship to the aziridine ring. T

Regiochemical Control of the Ring-Opening of 1,2-Epoxides by Means of Chelating Processes. 3. Aminolysis and Azidolysis of the cis- and trans-Oxides Derived from 4-(Benzyloxy)cyclohexene

The previously observed regiocontrol of the ring-opening of epoxides bearing a remote polar group such as the title compounds (1 and 2) can also be achieved by metal-assisted methods for the direct aminolysis and azidolysis of epoxides.The appropriate use