100200-70-2Relevant articles and documents
Regioselective addition of pyrrole to N-tosyl imines in the presence of Cu(OTf)2
Temelli, Baris,Unaleroglu, Canan
, p. 7941 - 7943 (2005)
The Cu(OTf)2 catalysed reaction of pyrrole with N-tosyl imines gives pyrrole sulfonamides in high yields. The addition reaction takes place regioselectively at C(2) of the pyrrole. The procedure is simple and does not require anhydrous conditio
The diastereoselective synthesis of 2,3-diaryl-3-cyano-substituted pyrrolidines via the MgI2 mediated ring expansion of aryl cyclopropyl nitriles
Stead, Darren
supporting information, (2020/09/04)
The MgI2 mediated reaction of aryl substituted cyclopropyl nitriles with tosyl aldimines to give 2,3-diaryl-3-cyano-substituted pyrrolidines has been demonstrated. In all cases, the trans-diastereoisomer was determined to be the major product.
Synthesis of novel N-(p-toluenesulfonyl)aminophosphonates and evaluation of their biological properties
Karpowicz, Rafa?,Lewkowski, Jaros?aw,Stasiak, Ma?gorzata,Czopor, Aleksandra,Tokarz, Paulina,Król, Adrianna,Rogacz, Diana,Rychter, Piotr
, p. 423 - 436 (2018/02/06)
The synthesis of a series of N-sulfonylaminophosphonates 2aA-2dC and evaluation of their cytotoxicity and ecotoxicity is described. N-sulfonylaminophsophonates 2aA-2dC were obtained by addition of dialkyl phosphites to azomethine bonds of sulfonimines 1a-
