Synthesis of tetrahydroisoquinoline with a 1,4-bridged 10-membered sulfur containing macrolactone (5) is described. Phenolic aldolisation, Pictet¿Spengler cyclisation of an acid sensitive amino diol under newly developed conditions (LiBr, toluene¿TFE, 80 °C) and acid promoted intramolecular C¿S bond formation leading to a 10-membered cycle are key steps of our synthesis
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