A convenient synthesis of 1-benzyl-1, 2, 3, 4-tetrahydroisoquinolines by combined Strecker/Bruylants reaction
E Reimann, C Ettmayr
Index: Reimann, Eberhard; Ettmayr, Christian Monatshefte fur Chemie, 2004 , vol. 135, # 10 p. 1289 - 1295
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Citation Number: 17
Abstract
Summary. Strecker reaction of iodophenethylamines with phenylacetaldehydes afforded the corresponding α-aminonitriles, which on treatment with i-propyl magnesium chloride underwent a Bruylants reaction to give the title compounds. Their structures were deduced by NMR and by an independent preparation starting from papaverine. The educts were easily available by standard procedures.
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