Synthesis of α-aminoketones via selective reduction of acyl cyanides
作者:Andreas Pfaltz、Saeed Anwar
DOI:10.1016/s0040-4039(01)81341-1
日期:1984.1
Reduction of acyl cyanides with zinc in acetic acid in the presence of excess acetic anhydride leads to N-acetyl-α-aminoketones in good yields. An efficient three-step synthesis of 5-aminolevulinic acid by this method is described.
PFALTZ, A.;ANWAR, SAEED, TETRAHEDRON LETT., 1984, 25, N 28, 2977-2980
作者:PFALTZ, A.、ANWAR, SAEED
DOI:——
日期:——
PROTEASE INHIBITORS
申请人:SMITHKLINE BEECHAM CORPORATION
公开号:EP0983228A1
公开(公告)日:2000-03-08
EP0983228A4
申请人:——
公开号:EP0983228A4
公开(公告)日:2002-08-07
[EN] PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTEASES
申请人:SMITHKLINE BEECHAM CORPORATION
公开号:WO1998050342A1
公开(公告)日:1998-11-12
(EN) The present invention provides bis-aminomethylcarbonyl compounds that are inhibitors of cysteine and serine proteases. The compounds are particularly useful for treating diseases in which excess cysteine protease activity has been implicated, including osteoporosis, periodontitis and arthritis.(FR) L'invention porte sur des composés de bis-aminométhylcarbonyl inhibiteurs des protéases de la cystéine et de la sérine. Lesdits composés s'avèrent particulièrement utiles pour traiter les maladies impliquant un excès d'activité de la protéase de la cystéine, dont l'ostéoporose, la périodontite ou l'arthrose.