An efficient method for opening nonactivated aziridines with TMS azide: application in the synthesis of chiral 1,2-diaminocyclohexane
摘要:
A variety of N-substituted aziridines have been opened with TMS azide in MeCN at rt in the absence of any Lewis acid. The reaction was extended to the synthesis of (R,R)- and (S,S)-1,2-diaminocyclohexane. (C) 2000 Elsevier Science Ltd. All rights reserved.
Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions
作者:R.Vijaya Anand、Ghanshyam Pandey、Vinod K. Singh
DOI:10.1016/s0040-4039(02)00727-x
日期:2002.5
A variety of aziridines were opened in an efficient manner with aromatic amines using silica gel under solvent free conditions.
使用无溶剂条件下的硅胶,可以用芳香胺有效地打开各种氮丙啶。
Efficient Method for Cleavage of Aziridines with Aromatic Amines
作者:Govindasamy Sekar、Vinod K. Singh
DOI:10.1021/jo981869r
日期:1999.4.1
An efficient method for opening nonactivated aziridines with TMS azide: application in the synthesis of chiral 1,2-diaminocyclohexane
作者:M Chandrasekhar、G Sekar、Vinod K Singh
DOI:10.1016/s0040-4039(00)01793-7
日期:2000.12
A variety of N-substituted aziridines have been opened with TMS azide in MeCN at rt in the absence of any Lewis acid. The reaction was extended to the synthesis of (R,R)- and (S,S)-1,2-diaminocyclohexane. (C) 2000 Elsevier Science Ltd. All rights reserved.
Mild and Efficient Method for Regioselective Ring Opening of Aziridines with Amines by Bismuth Trichloride