“…Cyclizations of the chiral iminium salt (4) with base afforded the carbinolamine ether (5) reduction of which with benzylic cleavage yielded (6, R = H). 13 The cyclization of the vinyl sulphoxides (7) and (8), obtained by Wittig reaction from the corresponding aldehyde, was achieved by base, when the 2isomer (7) gave the tetrahydroisoquinoline (9) and the E-isomer (8) yielded the enantiomer of (9). Desulphurizing reduction of (9) yielded 5-( -)-carnegine (6, R = Me) and desulphurization of its enantiomer gave R-( +)-carnegine.I4 Mescaline and homoveratrylamine have been converted by Pictet-Spengler cyclization with the masked aldehydes (10) and ( I I ) respectively into anhalinine (12, R1 = OMe, R2 = H)15 and calycotomine (12, R1 = H, R2 = CH20H).…”