EnantioselectiveMichaelAddition of the 2-(1-Ethylpropoxy)acetaldehyde toN-[(1Z)-2-Nitroethenyl]acetamide - Optimization of the Key Step in the Organocatalytic Oseltamivir Synthesis-Reference-Cited by-同舟云学术

EnantioselectiveMichaelAddition of the 2-(1-Ethylpropoxy)acetaldehyde toN-[(1Z)-2-Nitroethenyl]acetamide - Optimization of the Key Step in the Organocatalytic Oseltamivir Synthesis

Published:2012-12 Issue:12 Volume:95 Page:2421-2428
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Hajzer Viktória,Latika Attila,Durmis Július,Šebesta Radovan

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/hlca.201200527/fullpdf

Reference30 articles.

1. Discovery and Development of GS 4104 (oseltamivir) An Orally Active Influenza Neuraminidase Inhibitor

2. Anti-influenza virus agents: Synthesis and mode of action

3. Synthetic Approaches to the Neuraminidase Inhibitors Zanamivir (Relenza) and Oseltamivir Phosphate (Tamiflu) for the Treatment of Influenza

4. Recent synthetic approaches to oseltamivir phosphate (Tamiflu™) for the treatment of influenza

5. Recent Development in Synthetic Strategies for Oseltamivir Phosphate

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