916754-53-5Relevant academic research and scientific papers
Stereoselective disposition of the geminal dimethyl group in the cyclization of geranyl acetate under zeolite confinement conditions
Tsangarakis, Constantinos,Stratakis, Manolis
, p. 4435 - 4439 (2007/10/03)
The stereochemistry in the acid-catalysed biomimetic cyclization of [8,8,8-D3]geranyl acetate was examined in solution and under conditions of zeolite Y confinement. In the intrazeolite reaction the gem-allylic methyl group adopts a diastereose
