Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation

スポンサーリンク

概要

論文の詳細を見る
1996-06-25

著者

関連論文

Synthesis and antimetastatic activity of 6-Trichloracetamido and 6-Guanidino Analogues of Siastatin B
Inhibition of Mouse Tumor Metastasis with Nojirimycin-related Compounds
Binding of Benanomicin A to Fungal Cells in Reference to its Fungicidal Action
New Bellenamine Homologs Inhibiting Human Immunodeficiency Virus Type 1 Infectivity
Layer Compression Modulus in Smectic Liquid Crystals
Layer Compression Modulus of Chiral Smectic Liquid Crystals Showing V-shaped Switching : Structure and Mechanical and Thermal Properties of Condensed Matter
2A_g Exciton State below 1B_u Exciton State in Trans-Polyacetylene Observed by Second-Harmonic-Generation Spectroscopy
Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum II. Physico-chemical Properties and Structure Elucidation
PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum I. Taxonomy of Producing Strain, Fermentation, Isolation and Biological Activities
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
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 (±)-PF1092A, B, and C; New Nonsteroidal Progesterone Receptor Ligands
Studies on the Biosynthesis of Bialaphos. Biochemical Mechanism of C-P Bond Formation: Discovery of Phosphonopyruvate Decarboxylase which Catalyzes the Formation of Phosphonoacetaldehyde from Phosphonopyruvate
Biochemical Mechanism of C-P Bond Formation of Bialaphos : Use of Gene Manipulation for the Analysis of the C-P Bond Formation Step(Biological Chemistry)
Synthesis and Insecticidal Activity of New 2- and 6-Substituted 4-Acetoxyquinolines
New Insecticidal 4-Acetoxy-2-alkenylquinolines
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

もっと見る

スポンサーリンク