113296-80-3Relevant articles and documents
One-pot α-amidosulfone-mediated variation of the pictet-Spengler tetrahydroisoquinoline synthesis, suitable for amide-type substrates
Arroyo, Francisco J.,López-Alvarado, Pilar,Ganesan,Menéndez, J. Carlos
, p. 5720 - 5727 (2014/11/07)
The development of Pictet-Spengler reactions from amide substrates is a challenging problem. We report here that the reaction between amide-type compounds (including carbamates, amides, ureas and diketopiperazines), aldehydes and p-toluenesulfinic acid constitutes an efficient method for the preparation of tetrahydroisoquinolines or pyrazino-[2,1-b]isoquinolines. Unlike previously known methods, this one-pot Pictet-Spengler protocol avoids the need for strong Lewis or Br?nsted acid catalysts.
Preparations and reactions of (Z)-3-arylidene-6-arylmethyl-2,5-piperazinediones having highly oxygenated benzene rings
Kubo,Saito,Yamato,Kawakami
, p. 2525 - 2532 (2007/10/02)
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