1133452-77-3Relevant academic research and scientific papers
Conversion of N-benzyloxycarbonylamino- and N-Tosylamino-benzyl phenylsulfones by green Strecker reactions to α-aminobenzyl nitriles using potassium hexacyanoferrate(II)
Hu, Xiaochun,Li, Rongzhi,Li, Zheng
, p. 432 - 436 (2014)
The cyanation of aldimines, generated in situ from N- benzyloxycarbonylamino- and N-tosylamino-benzyl phenylsulfones, to the corresponding N-protected a-aminobenzyl nitriles has been achieved by eco-friendly Strecker reactions using potassium hexacyanofer
A mild and efficient catalytic Strecker reaction of N-alkoxycarbonylamino sulfones with trimethylsilyl cyanide using indium(III) chloride: A facile synthesis of α-aminonitriles
Das, Biswanath,Damodar, Kongara,Shashikanth, Boddu,Srinivas, Yallamalla,Kalavathi, Itikala
experimental part, p. 3133 - 3136 (2009/06/17)
The Strecker reaction of N-alkoxycarbonylamino sulfones with trimethylsilyl cyanide in the presence of catalytic amount of indium(III) chloride at room temperature produces the corresponding protected α;-aminonitriles in high yields. Georg Thieme Verlag Stuttgart.
