127987-33-1

Upstream product

• 84029-18-5 (1RS,3RS,6SR)-3-(benzyloxy)-7-oxabicyclo[4.1.0]heptane 
• 917-54-4 methyllithium 
• 84049-33-2 (1SR,3RS,6RS)-3-(benzyloxy)-7-oxabicyclo[4.1.0]heptane 
• 445481-11-8 (1S*,2R*,4S*)-4-(benzyloxy)-1,2-epoxycyclohexane 

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

Alternating high regioselection in methyl group transfer to alicyclic oxiranes. Significance of the presence of a remote polar group

An alternating high regiocontrol of the methylating ring opening of oxiranes 1 and 2 by means of metal-assisted chelating or non-chelating processes is reported.