Tai-shun Lin

发表

Synthesis of 2′,3′-Unsaturated and 2′, 3′-Dideoxy Analogs of 6-Azapyrimidine Nucleosides as Potential Anti-Hiv Agents

Tai-Shun Lin, Jing-Hua Yang, You-Song Gao, 1990 .

SYNTHESIS AND ANTICANCER AND ANTIVIRAL ACTIVITY OF CERTAIN PYRIMIDINE NUCLEOSIDE ANALOGUES

Tai-shun Lin, Mao Liu, T. Lin, 1993 .

2,3-DIMETHYL-1,4-NAPHTHOQUINONE DERIVATIVES AS BIOREDUCTIVE ALKYLATING AGENTS WITH CROSSLINKING POTENTIAL

A. Sartorelli, I. Antonini, Tai-shun Lin, 1984 .

Structural Features of 2′,3′-Dideoxy-2′,3′-Didehydrocytidine, A Potent Inhibitor of the HIV (AIDS) Virus

W. Prusoff, G. Birnbaum, Tai-shun Lin, 1989 .

Experimental Aspects of Antiviral Pharmacology

W. Prusoff, Tai-shun Lin, T. Lin, 1988 .

Overview of the Possible Targets for Viral Chemotherapy

M. Otto, W. Prusoff, Tai-shun Lin, 1984 .

Synthesis of 2′,3′-Dideoxy-2′-methylene Pyrimidine Nucleosides as Potential Anti-Human Immunodeficiency Virus (HIV) Agents

Tai-shun Lin, M. Luo, Mao Liu, 1992 .

Synthesis of [2‐14C] 3′‐deoxythymidin‐2′ ‐ENE (d4T) and [5–125I] 3′ ‐azido‐2′, 3′‐dideoxy‐5‐iodouridine: Potent inhibitors of human immunodeficiency virus (HIV‐1)

W. Prusoff, H. Qian, E. M. August, 1989 .

Design and Synthesis of 2‘,3‘-Dideoxy- 2‘,3‘-didehydro-β-l-cytidine (β-l-d4C) and 2‘,3‘-Dideoxy-2‘,3‘-didehydro-β-l-5- fluorocytidine (β-l-Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in Vitro

E. Gullen, G. Dutschman, Tai-shun Lin, 1996 .

1 Chemical and Biological Properties of Cytotoxic α-(N)-Heterocyclic Carboxaldehyde Thiosemicarbazones

A. Sartorelli, Tai-shun Lin, Mao Liu, 1995 .

Synthesis and Biological Evaluation of 1,3-Oxathiolane 5-Azapyrimidine, 6-Azapyrimidine, and Fluorosubstituted 3-Deazapyrimidine Nucleosides

Maohui Luo, A. Sartorelli, E. Gullen, 2000, Nucleosides, Nucleotides & Nucleic Acids.

Synthesis of 4-(O-Arylsulfonyl)quinoline-5,8-quinones

A. Sartorelli, Tai-shun Lin, M. Fernández, 1989 .

A One-Pot Synthesis of 3-Nitro-and 3,5-Dinitro-2-Picolines

A. Sartorelli, Tai-shun Lin, Mao Liu, 1990 .

Synthesis of 1-β-L-Arabinofuranosylcytosine (β-L-Ara-C) and 2′-Deoxy-2′-methylene-β-L-cytidine (β-L-DMDC) as Potential Antineoplastic Agents

Tai-shun Lin, M. Luo, Mao Liu, 1994 .

MOLECULAR BASIS FOR SERENDIPITOUS DEVELOPMENT OF ANTIVIRAL AND ANTICANCER AMINONUCLEOSIDES

R. Schinazi, W. Prusoff, P. Fischer, 1979 .

SYNTHESIS, ANTIVIRAL ACTIVITY, AND MECHANISM OF ACTION OF A NOVEL SERIES OF PYRIMIDINE NUCLEOSIDE ANALOGS

D. Ward, W. Prusoff, Tai-shun Lin, 1978 .

Synthesis of 1-[cis-2-Hydroxy-cis-3-(hydroxymethyl)-cyclobutyl]thymine, a Novel Method for the Synthesis of Cyclobutyl Nucleosides and Related Compounds

Tai-shun Lin, M. Luo, Mao Liu, 1994 .

SYNTHESIS OF NITRONUCLEOSIDES

Tai-shun Lin, R. E. Harmon, T. Lin, 1975 .

1-(2,3-Dideoxy-β-D-glycero-pent-2-enofuranosyl)thymine. A Highly Potent and Selective Anti-HIV Agent.

J. Starrett, W. Prusoff, J. Sommadossi, 1989 .

5-Iodo-2′-Deoxyuridine

W. Prusoff, P. Fischer, Ming S. Chen, 1979 .

Effect of 5-Iodo-5′-Amino-2′,5′-Dideoxyuridine on Varicella-Zoster Virus In Vitro

F. Rapp, W. Prusoff, Tai-shun Lin, 1979, Antimicrobial Agents and Chemotherapy.

Pharmacological considerations of antiviral agents

W. Prusoff, Tai-shun Lin, S. Siegel, 1984 .