proline and oseltamivir

proline has been researched along with oseltamivir in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hayashi, Y; Ishikawa, H; Suzuki, T1
Hayashi, Y; Ishikawa, H; Orita, H; Suzuki, T; Uchimaru, T1
Razonable, RR1
Hayashi, Y; Ogasawara, S1

Reviews

1 review(s) available for proline and oseltamivir

ArticleYear
Antiviral drugs for viruses other than human immunodeficiency virus.
    Mayo Clinic proceedings, 2011, Volume: 86, Issue:10

    Topics: Acyclovir; Adenine; Amantadine; Antiviral Agents; Comorbidity; Drug Therapy, Combination; Foscarnet; Ganciclovir; Guanine; Hepatitis; Hepatitis B, Chronic; Hepatitis C; Herpesviridae Infections; HIV Infections; Humans; Influenza, Human; Interferons; Lamivudine; Nucleosides; Oligopeptides; Organophosphonates; Oseltamivir; Proline; Protease Inhibitors; Pyrimidinones; Ribavirin; Telbivudine; Thymidine; Valacyclovir; Valganciclovir; Valine; Virus Replication; Zanamivir

2011

Other Studies

3 other study(ies) available for proline and oseltamivir

ArticleYear
High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations.
    Angewandte Chemie (International ed. in English), 2009, Volume: 48, Issue:7

    Topics: Animals; Antiviral Agents; Catalysis; Ethers; Humans; Influenza, Human; Oseltamivir; Proline; Stereoisomerism

2009
High-yielding synthesis of the anti-influenza neuraminidase inhibitor (-)-oseltamivir by two "one-pot" sequences.
    Chemistry (Weinheim an der Bergstrasse, Germany), 2010, Nov-08, Volume: 16, Issue:42

    Topics: Antiviral Agents; Catalysis; Combinatorial Chemistry Techniques; Ethers; Humans; Molecular Structure; Neuraminidase; Oseltamivir; Proline; Stereoisomerism

2010
Time Economical Total Synthesis of (-)-Oseltamivir.
    Organic letters, 2016, 07-15, Volume: 18, Issue:14

    Topics: Antiviral Agents; Catalysis; Efficiency; Ethers; Formates; Oseltamivir; Proline; Stereoisomerism; Thiourea

2016