Model Study for Preparation of asymmetric N, N'-Disubstituted piperazine Library:Efficient Synthesis of Aryl Piperazine and Benzyl Piperazine Derivatives on the Solid Support
スポンサーリンク
概要
- 論文の詳細を見る
- 1998-05-05
著者
-
AJITO Keiichi
Pharmaceutical Research Center, Meiji Seika Kaisha, Ltd.
-
Ajito K
Meiji Seika Kaisha Ltd. Yokohama Jpn
-
Ajito Keiichi
Pharmaceutical Research Center Meiji Seika Kaisha Ltd.
-
OHTSUKA Yasuo
Pharmaceutical Research Center, Meiji Seika, Ltd.
-
Ohtsuka Yasuo
Pharmaceutical Research Center Meiji Seika Ltd.
-
Ohtsuka Y
Pharmaceutical Research Center Meijiseika Kaisha Ltd.
-
YAMAMOTO Yasuo
Pharmaceutical Research Center, Meiji Seika Kaisha, Ltd.
-
Yamamoto Yasuo
Pharmaceutical Research Center Meiji Seika Kaisha Ltd.
-
Yamamoto Yasuo
Pharmaceutical Research Center Meijiseika Kaisha Ltd.
関連論文
- Synthesis of SF2809-V, Chymase Inhibitor, and Its Analogs by Three Component Reaction : Model Study for High Throughput Synthesis of a Chymase Inhibitor Library
- Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
- PF1163A and B, New Antifungal Antibiotics Produces by Penicilium sp. II. Physico-chemical Properties and Structure Elucidation
- PF1163A and B, New Antifungal Antibiotics Produced by Penicilium sp. : II. Physico-chemical Properties and Structure Elucidation
- Novel Azalides Derived from Sixteen-Membered Macrolides : I. Isolation of the Mobile Dialdehyde and Its One-Pot Macrocyclization with an Amine
- Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position I. Epimerization and Methylation of the 3-Hydroxyl Group
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics VI. Synthesis of metabolically Programmed, Highly Potent Analogues of Sixteen-membered Macrolide Antibiotics
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics V. Preparation of Unsubstituted L-Cladinose Analogues: Effect of Methylation of a 3''-Hydroxyl Group on the Bioactivity
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics II. Preparation of Pharmacokinetically Improved Analogues via Biotransformation
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation
- Application of Polymer Supported Base in Solid Phase Synthesis: Convenient Synthesis of N-Aryl-N'-benzyl Piperazine Derivatives
- Model Study for Preparation of asymmetric N, N'-Disubstituted piperazine Library:Efficient Synthesis of Aryl Piperazine and Benzyl Piperazine Derivatives on the Solid Support
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics III. Efficient Synthesis of 4-0-Alkyl-L-cladinose Analogues: Improved Antibacterial Activities Compatible with Pharmacokinetics
- Synthesis of Potent α_vβ_3/α_β_3 Dual Antagonists Tricyclic Pharmacophore-based Molecules and Their Selectivity Control
- Synthesis of novel lincomycin derivatives and their in vitro antibacterial activities