1414889-09-0Relevant articles and documents
Organocatalytic enantioselective Strecker reaction of cyclic trifluoromethyl-ketoimines
Xie, Hexin,Song, Aiguo,Song, Xixi,Zhang, Xinshuai,Wang, Wei
supporting information, p. 1409 - 1411 (2013/04/23)
A quinine thiourea promoted enantioselective Strecker reaction of cyclic ketoimines with TMSCN has been developed. The process affords new enantioenriched trifluoromethyl dihydroquinazolinones in high yields and with high enantioselectivities. Copyright
Highly enantioselective organocatalytic Strecker reaction of cyclic N-acyl trifluoromethylketimines: Synthesis of anti-HIV drug DPC 083
Zhang, Fa-Guang,Zhu, Xiao-Yan,Li, Shen,Nie, Jing,Ma, Jun-An
supporting information, p. 11552 - 11554,3 (2012/12/12)
A highly efficient, organocatalytic, enantioselective Strecker reaction of cyclic N-acyl ketimines was developed for the preparation of enantioenriched cyclic α-amino nitriles with a quaternary carbon stereocentre and anti-HIV drug DPC 083. This journal is
Highly enantioselective organocatalytic Strecker reaction of cyclic N-acyl trifluoromethylketimines: Synthesis of anti-HIV drug DPC 083
Zhang, Fa-Guang,Zhu, Xiao-Yan,Li, Shen,Nie, Jing,Ma, Jun-An
supporting information, p. 11552 - 11554 (2013/01/15)
A highly efficient, organocatalytic, enantioselective Strecker reaction of cyclic N-acyl ketimines was developed for the preparation of enantioenriched cyclic α-amino nitriles with a quaternary carbon stereocentre and anti-HIV drug DPC 083. The Royal Society of Chemistry 2012.