John C. Martin

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Synthesis and Anti‐HIV Activity of Several 2′‐Fluoro‐Containing Pyrimidine Nucleosides.

M. Mansuri, I. Ghazzouli, V. Brankovan, 1991 .

A potentially simple 13C NMR method to assign regio- and stereochemistry of (2′-deoxy-2′-fluoroarabinofuranosyl) nucleosides.

M. Mansuri, John C. Martin, B. Krishman, 1991 .

Chapter 14. Antiviral Agents

M. Mansuri, John C. Martin, 1991 .

CAN CURCUMIN PREVENT Alzheimer ' s Curcumin

John C. Martin, Curcumin Prevent, 2004 .

Early nucleoside reverse transcriptase inhibitors for the treatment of HIV: a brief history of stavudine (D4T) and its comparison with other dideoxynucleosides.

E. De Clercq, W. Prusoff, M. Hitchcock, 2010, Antiviral research.

Comparative Studies of 2′,3′‐Didehydro‐2′,3′‐Dideoxythymidine (D4T) with other Pyrimidine Nucleoside Analogues

S. Kaul, A. Fridland, L. Dunkle, 1990, Annals of the New York Academy of Sciences.

The use of acetyl bromide for the multigram synthesis of the anti-HIV agent 2',3'-didehydro-2',3'-dideoxycytidine (d4C)

J. Starrett, D. Tortolani, D. Baker, 1990 .

A Short Syhthesis of 3′-(Methylsulfinyl)-3′-Deoxythymidine and Related Analogues

J. Wos, M. Mansuri, John C. Martin, 1989 .

Phosphonate Isosteres of 2′,3′-Didehydro-2,3-dideoxynucleoside Monophosphates: Synthesis and Anti-HIV Activity

C. Kim, John C. Martin, B. Luh, 1991 .

Synthesis of 2′,3′-Dideoxyinosine

R. Webb, J. Wos, John C. Martin, 1988 .

Regiospecific and Highly Stereoselective Electrophilic Addition to Furanoid Glycals: Synthesis of Phosphonate Nucleotide Analogues with Potent Activity Against HIV.

C. Kim, John C. Martin, B. Luh, 1991 .

Regiospecific and highly stereoselective electrophilic addition to furanoid glycals: synthesis of phosphonate nucleotide analogs with potent activity against HIV

C. Kim, John C. Martin, B. Luh, 1991 .

Selected Thoughts on Hydrophobicity in Drug Design

L. Lou, John C. Martin, 2021, Molecules.

Synthesis and biological activity of carbocyclic derivatives of the potent antiviral agent 9-[2-(phosphonomethoxy)ethyl]guanine (PMEG)

J. Bronson, M. Mansuri, John C. Martin, 1992 .

Synthesis and HIV activity of phosphonate isosteres of D4T monophosphate

J. Bronson, C. Kim, John C. Martin, 1992 .

Synthesis and Antiviral Activity of Nucleotide Analogues Bearing the ( S)-(3-Hydroxy-2-phosphonylmethoxy)propyl Moiety Attached to Adenine, Guanine, and Cytosine

R. Webb, E. Kern, J. Bronson, 1991 .

A Convenient Synthesis of S‐HPMPA (I).

R. Webb, John C. Martin, 1988 .

Perspectives on the development of acyclic nucleotide analogs as antiviral drugs.

William A. Lee, John C. Martin, 2006, Antiviral research.

SYNTHESIS OF PYRIDINES FROM DICYANOPYRIMIDINES. A DIELS‐ALDER APPROACH TO THE C‐RING OF STREPTONIGRIN

John C. Martin, 1980 .

One step synthesis of 3,8-methanoaza[10]annulene derivatives

M. L. Maddox, J. Muchowski, John C. Martin, 1980 .

Synthesis and Antiviral Evaluation of 3′-Branched Nucixoside Analogues

M. Wittman, M. Hitchcock, Hyekyung Yang, 1991 .

Synthesis of the 7-deaza and 5-aza-7-deaza purine analogs of the antiherpes agent 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine (DHPG)

D. McGee, John C. Martin, J. Verheyden, 1985 .

Chapter 17. Antiviral Agents

M. Mansuri, John C. Martin, 1988 .

Synthesis and Antiviral Activity of the 3-Deaza Analogue of 9-((1, 3-Dihydroxy-2-propoxy)Methyl)Guanine

D. Smee, D. McGee, John C. Martin, 1990 .

A novel and stereospecific synthesis of (.+-.)- and (-)-aristeromycin

John C. Martin, G. Madhavan, 1986 .

Total synthesis of the methyl ester of the 9,11-dithia analog of 13,14-dehydro-PGH2

Soumitra S Ghosh, J. Fried, John C. Martin, 1987 .

Antiherpes Simplex Virus Activity of 9-[4-Hydroxy-3-(hydroxymethyl)-1-butyl] guanine

D. Smee, John C. Martin, J. Verheyden, 1984 .

Synthesis of 1,3-diamino-2-hydroxypropane derivatives as pseudosymmetric HIV protease inhibitors

W. Harte, Kuo-Long Yu, M. Mansuri, 1993 .

Nucleotide analogues as antiviral agents

John C. Martin, 1989 .

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 .

Biochemical Pharmacology of Acyclic Nucleotide Analogues

H. Ho, J. Bronson, M. Hitchcock, 1990, Annals of the New York Academy of Sciences.

A New Synthesis of the Potent and Selective Anti-Herpesvirus Agent (S)-1-[3-Hydroxy-2-(Phosphonylmethoxy)Propyl]Cytosine

H. G. Howell, J. Bronson, John C. Martin, 1990 .

Synthesis of 9-[(Phosphonomethoxy)methyl]guanine and 9-[2-Hydroxy-1-(phosphonomethoxy)ethyl]guanine

C. Kim, John C. Martin, P. F. Misco, 1990 .

Synthesis of 4′-(Hydroxymethyl)Guanosine and a Phosphonate Analogue of Guanylic Acid

John C. Martin, J. Verheyden, 1988 .

Synthesis and Anti-Herpes-Virus Activity of Acyclic 2′-Deoxyguanosine Analogues Related to 9-((1,3-Dihydroxy-2-propoxy)methyl)guanine.

D. Smee, D. Hobbs, D. McGee, 1987 .

Heterogeneity of HLA-A,B, Ia-like, and Melanom Expression by Human Melanoma Cell Lines Analyzed with Monoclonal Antibodies and Flow Cytometry

S. Ferrone, N. Warner, John C. Martin, 1982 .

A novel synthesis of 1-OXA-HPMPA: a potent antiviral agent against herpesviruses

C. Kim, John C. Martin, B. Luh, 1992 .

A Novel Synthesis of 1‐Oxa‐HPMPA (I): A Potent Antiviral Agent Against Herpesviruses.

C. Kim, John C. Martin, B. Luh, 1992 .

A HETEROCYCLIC DIELS-ALDER APPROACH TO THE SYNTHESIS OF THE PYRIDINE C RING OF STREPTONIGRIN

John C. Martin, 1982 .

Chapter 15 Antiviral Agents

M. Mansuri, John C. Martin, 1987 .

Preparation of the geometric isomers of DDC, DDA, D4C and D4T as potential anti-HIV agents

J. Starrett, V. Farina, M. Mansuri, 1991 .

Preparation of the Geometric Isomers (I) ‐ (IV) of DDC, DDA, D4C, and D4T as Potential anti‐HIV Agents.

J. Starrett, V. Farina, M. Mansuri, 1992 .

Acyclic nucleoside analogues: methods for the preparation of 2′,3′-secoguanosine, 5′-deoxy-2′,3′-secoguanosine, and(R,S)-9-[1-(2-hydroxyethoxy)-2-hydroxyethyl]guanine

D. McGee, John C. Martin, 1986 .

Preparation of 1-(2,3-dideoxy-.beta.-D-glycero-pent-2-enofuranosyl)thymine (d4T) and 2',3'-dideoxyadenosine (ddA): general methods for the synthesis of 2',3'-olefinic and 2',3'-dideoxy nucleoside analogs active against HIV

J. Starrett, D. Tortolani, H. G. Howell, 1989 .

Synthesis and Antiviral Activity of Phosphonylmethoxyethyl Derivatives of Purine and Pyrimidine Bases

E. Kern, J. Bronson, C. Kim, 1991 .

Preparation of 1-(2,3-Dideoxy-β-D-glycero-pent-2-enofuranosyl)thymine (d4T) and 2′,3′-Dideoxyadenosine (ddA): General Methods for the Synthesis of 2′,3′-Olefinic and 2′,3′-Dideoxy Nucleoside Analogues Active Against HIV.

J. Starrett, D. Tortolani, H. G. Howell, 1990 .

A Novel and Efficient Preparation of 21,31-Dideoxynucleosides1

John C. Martin, E. Prisbe, 1985 .

Synthesis, Anti-Hiv Activity, and Biological Properties of 2′,3′-Didehydro-2′,3′-Dideoxythwidine (d4T)

J. Starrett, H. Ho, J. Sommadossi, 1989 .

Synthesis of 9-((1,3-Dihydroxy-2-Propoxy)Methyl)Guanine (Dhpg) Via Condensation Of N2sp>u>9-Diacetylguanine With A Sulfinylmethyl Ether

D. McGee, John C. Martin, J. Verheyden, 1988 .

Synthesis of (S)-N1-(3-hydroxy-2-phosphonylmethoxy)propylcytosine, (S)-HPMPC

R. Webb, J. Bronson, J. Wos, 1988 .

Synthesis of 9-(4-hydroxy-2-oxobutyl)guanine, 9-(2,4-dihydroxybutyl)guanine and related acyclic nucleoside analogs

D. Smee, John C. Martin, J. Verheyden, 1985 .

Synthesis and Antiviral Activity of Methyl Derivatives of 9-(2-( Phosphonomethoxy)ethyl)guanine.

A. Patick, J. Bronson, R. Datema, 1992 .

Synthesis, Oral Bioavailability Determination, and in vitro Evaluation of Prodrugs of the Antiviral Agent 9‐(2‐(Phosphonomethoxy)ethyl) adenine (PMEA).

J. Starrett, D. Tortolani, J. Russell, 1994 .

Synthesis and Antiviral Activity of the Nucleotide Analogue (S)-1-(3-Hydroxy-2-(phosphonylmethoxy)propyl)cytosine.

R. Webb, J. Bronson, M. Hitchcock, 1989 .

9-(1,3-DIHYDROXY-2-PROPOXYMETHYL)GUANINE: A NEW POTENT AND SELECTIVE ANTIHERPES AGENT

D. Smee, John C. Martin, J. Verheyden, 1983 .

ACYCLIC ANALOGS OF 2′-DEOXYNUCLEOSIDES RELATED TO 9-((1,3-DIHYDROXY-2-PROPOXY)METHYL)GUANINE AS POTENTIAL ANTIVIRAL AGENTS

D. Smee, D. McGee, John C. Martin, 1985 .

A chemical chaperone improves muscle function in mice with a RyR1 mutation

Amy D. Hanna, Corey L. Reynolds, E. Sahin, 2017, Nature Communications.

1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-ethyluracil. A Highly Selective Antiherpes Simplex Agent.

Ming S. Chen, M. Mansuri, I. Ghazzouli, 1987 .

A convenient synthesis of -HPMPA

R. Webb, John C. Martin, 1987 .

Neutrophil count is the most important prognostic component of the differential white cell count in patients undergoing elective surgery for colorectal cancer.

D. McMillan, P. Horgan, D. G. Watt, 2015, American journal of surgery.

Synthesis of a phosphonate isostere of ganciclovir monophosphate: A highly cytomegalovirus active phosphonate nucleotide analogue

C. Kim, John C. Martin, B. Luh, 1990 .

Synthesis and anti-HIV activity of 9-[(2R-5R)-2,5-dihydro-5-(phosphonomethoxy)-2-furanyl]-2,6-diaminopurine

C. Kim, John C. Martin, B. Luh, 1992 .

Current concepts in antisense drug design.

J. C. Martin, J. Milligan, M. Matteucci, 1993, Journal of medicinal chemistry.

Cidofovir, a New Agent with Potent Anti-Herpesvirus Activity

J. C. Martin, H. Jaffe, R. Stagg, 1996 .

Intracellular metabolism of the antiherpes agent (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]cytosine.

J. C. Martin, H. Ho, H. de Boeck, 1992, Molecular pharmacology.

Synthesis, oral bioavailability determination, and in vitro evaluation of prodrugs of the antiviral agent 9-[2-(phosphonomethoxy)ethyl]adenine (PMEA).

J. C. Martin, J. Starrett, D. Tortolani, 1994, Journal of medicinal chemistry.