Stereoselective construction of trans-1,2-benzooxadecaline frameworks by three-component cascade reactions of an alpha-phenethyl-beta-borylallylsilane with aldehydes
M. Suginome et al., Stereoselective construction of trans-1,2-benzooxadecaline frameworks by three-component cascade reactions of an alpha-phenethyl-beta-borylallylsilane with aldehydes, CHEM COMMUN, (12), 2001, pp. 1090-1091
Reactions of alpha -phenethyl-beta -borylallylsilane with aldehydes afforde
d tricyclic trans- 1,2-benzooxadecaline frameworks stereoselectively in the
presence of Lewis acids via sequential incorporation of two different alde
hydes followed by cationic cascade cyclization, ending up with intramolecul
ar Friedel-Crafts reaction.