- Dendrimers ended by non-symmetrical azadiphosphonate groups: Synthesis and immunological properties
[作者:Marchand, P; Griffe, L; Poupot, M; Turrin, CO; Bacquet, G; Fournie, JJ; Majoral, JP; Poupot, R; Caminade, AM,期刊:Bioorganic & Medicinal Chemistry Letters, 页码:3963-3966 , 文章类型: Article,,卷期:2009年19-14]
- The synthesis and characterization of new series of phosphorus-containing dendrimers ended by nonsymmetrical azamonophosphonates, or azadiphosphonates, or azadiphosphonic acid salts are reported. The sodium salts of the ...
- Synthesis, configurational stability and stereochemical biological evaluations of (S)- and (R)-5-hydroxythalidomides
[作者:Yamamoto, T; Shibata, N; Sukeguchi, D; Takashima, M; Nakamura, S; Toru, T; Matsunaga, N; Hara, H; Tanaka, M; Obata, T; Sasaki, T,期刊:Bioorganic & Medicinal Chemistry Letters, 页码:3973-3976 , 文章类型: Article,,卷期:2009年19-14]
- The first asymmetric synthesis of (S)- and (R)-5-hydroxythalidomides, one of thalidomide's major metabolites, was achieved using HMDS/ZnBr2-induced imidation as a key reaction. 5-Hydroxythalidomide was found to be config...
- Synthesis and SAR study of novel pseudo-steroids as potent and selective progesterone receptor antagonists
[作者:Jain, N; Allan, G; Linton, O; Tannenbaum, P; Chen, X; Xu, J; Zhu, PF; Gunnet, J; Demarest, K; Lundeen, S; Murray, W; Sui, ZH,期刊:Bioorganic & Medicinal Chemistry Letters, 页码:3977-3980 , 文章类型: Article,,卷期:2009年19-14]
- Synthesis of novel 7-pseudo-steroids 1c has been achieved from trenbolone 3 via an efficient 14 step sequence with overall yields of 10-15%. Various substitutions were incorporated at both the aromatic side chain as well...
|