1202166-85-5Relevant academic research and scientific papers
Octahedra-based molecular sieve aluminoborate (PKU-1) as solid acid for heterogeneously catalyzed Strecker reaction
Wang, Weilu,Wang, Ying,Wu, Bin,Cong, Rihong,Gao, Wenliang,Qin, Bo,Yang, Tao
, p. 174 - 178 (2015)
An aluminoborate (PKU-1) with octahedron-based framework was found to be a highly efficient solid acid catalyst for the rapid and convenient synthesis of α-aminonitriles from imines and TMSCN under mild reaction conditions. The catalytic active sites are
Continuous solid solutions constructed from two isostructural octahedron-based molecular sieves: preparation, acidity regulation and catalytic application in Strecker reactions
Wang, Weilu,Zeng, Chunmei,Yang, Yao,Jiang, Pengfei,Gao, Wenliang,Cong, Rihong,Yang, Tao
, p. 18184 - 18192 (2019/12/02)
Strecker reactions have an important application in the preparation of α-amino acids and biologically active molecules in homogeneous acid- or base-catalyzed systems. As novel solid acid catalysts, AlxGa1-x-PKU-1 (x = 0-1) solid solu
Octahedron-based redox molecular sieves M-PKU-1 (M?=?Cr, Fe): A novel dual-centered solid acid catalyst for heterogeneously catalyzed Strecker reaction
Wang, Weilu,Zhang, Siyu,Hu, Shixiang,Wang, Duo,Gao, Wenliang,Cong, Rihong,Yang, Tao
, p. 240 - 251 (2017/06/13)
Cr-PKU-1, an octahedron-based redox molecular sieve, was found to be an efficient, environmentally benign and easily recoverable catalyst for the heterogeneously-catalyzed Strecker reaction under the mild conditions. This material was evidenced to be a du
Amberlyst-15 catalysed synthesis of N-tosyl-α-aminonitriles through Strecker reaction
Sudhakar, Dega,Rao, Vallabhaneni Madhava,Suresh, Maddila,Rao, Chunduri Venkata
experimental part, p. 12 - 14 (2010/05/19)
N-Tosyl-α-aminonitriles have been synthesised by a Strecker reaction of various N-tosyl aldimines with trimethylsilyl cyanide in the presence of catalytic amount of Amberlyst-15 polymer at room temperature under heterogeneous conditions.
Synthesis of α-aminonitriles through Strecker reaction of N-tosylaldimines using molecular iodine
Das, Biswanath,Balasubramanyam, Penagaluri,Krishnaiah, Maddeboina,Veeranjaneyulu, Boyapati,Reddy, Gandolla Chinna
experimental part, p. 3467 - 3471 (2010/02/28)
The Strecker reaction of N-tosylaldimines with trimethylsilyl cyanide in the presence of catalytic amount of iodine at room, temperature produces the corresponding protected α-aminonitriles in high yields.
