(PDF) Syntheses of 2-Deoxy-2,3-Didehydro-N-Acetylneuraminic

Syntheses of 2-Deoxy-2,3-Didehydro-N-Acetylneuraminic Acid Analogues Modified by ^|^#945;-Acylaminoamido Groups at the C-4 Position Using Isocyanide-Based Four-Component Coupling and Biological Evaluation as Inhibitors of Human Parainfluenza Virus Type 1

Chemical and Pharmaceutical Bulletin - Japan

doi 10.1248/cpb.c12-00834

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January 1, 2013

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Pharmaceutical Society of Japan

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Amanote Research

Syntheses of 2-Deoxy-2,3-Didehydro-N-Acetylneuraminic Acid Analogues Modified by ^|^#945;-Acylaminoamido Groups at the C-4 Position Using Isocyanide-Based Four-Component Coupling and Biological Evaluation as Inhibitors of Human Parainfluenza Virus Type 1

Chemical and Pharmaceutical Bulletin - Japan

doi 10.1248/cpb.c12-00834

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Isocyanide-Based Four-Component Synthesis of Benzo[a]pyrano[2,3-C]phenazines

Targeting Human Parainfluenza Virus Type-1 Haemagglutinin-Neuraminidase With Mechanism-Based Inhibitors

Stereoselective Synthesis and Biological Evaluations of Novel 3′-Deoxy-4′-Azaribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication

N, N-Bisbenzylidenebenzene-1, 4-Diamines and N, N-Bisbenzylidenenaphthalene-1, 4-Diamines as Sirtuin Type 2 (SIRT2) Inhibitors

Biological Evaluation of 2,3-Dioxoindolin-N-Phenylacetamide Derivatives as Potent CDC25B and PTP1B Phosphatase Inhibitors

Synthesis of Sialic Acid Derivatives Having Inhibitory Activities Against Human Parainfluenza Virus Type 1

Synthesis and Biological Properties of 1.beta.-Methyl-Carbapenems With N-Methylpyrrolidinylthio Group at C-2 Position.

Design, Synthesis, Biological and Structural Evaluation of Functionalized Resveratrol Analogues as Inhibitors of Quinone Reductase 2