Karl Grozinger
Sacred Heart University(US)
Publications by Year
Research Areas
HIV/AIDS drug development and treatment, Chemical Synthesis and Analysis, HIV Research and Treatment, Asymmetric Synthesis and Catalysis, Carbohydrate Chemistry and Synthesis
Most-Cited Works
- → Inhibition of HIV-1 Replication by a Nonnucleoside Reverse Transcriptase Inhibitor(1990)746 cited
- → Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo- and dipyridodiazepinones(1991)208 cited
- → Inhibition of Human Immunodeficiency Virus Type I (HIV-I) Replication by the Dipyridodiazepinone BI-RG-587(1991)110 cited
- → Synthesis of (1R,2S)-1-Amino-2-vinylcyclopropanecarboxylic Acid Vinyl-ACCA) Derivatives: Key Intermediates for the Preparation of Inhibitors of the Hepatitis C Virus NS3 Protease(2005)87 cited
- → A Selective, Mild Clevage of Trichloroethyl Esters, Carbamates, and Carbonates to Carboxylic Acids, Amines, and Phenols using Zinc/Tetrahydrofuran/pH 4.2-7.2 Buffer(1976)72 cited
- → Cross-coupling of 1-aryl-5-bromopyrazoles: regioselective synthesis of 3,5-disubstituted 1-arylpyrazoles(2000)65 cited
- → Inhibition of human leukocyte elastase (HLE) by N-substituted peptidyl trifluoromethyl ketones(1992)48 cited
- → A significantly improved condition for cyclization of phenethylcarbamates to N-alkylated 3,4-dihydroisoquinolones(1998)45 cited
- → C -Nucleosides and Related Compounds. IV. The Synthesis and Chemistry of D,L-2,5-Anhydroallose Derivatives(1975)39 cited
- → Novel Non-nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase. 4. 2-Substituted Dipyridodiazepinones as Potent Inhibitors of Both Wild-Type and Cysteine-181 HIV-1 Reverse Transcriptase Enzymes(1995)38 cited