T. Obara

发表

Antiviral activities of ribavirin, 5-ethynyl-1-beta-D-ribofuranosylimidazole-4-carboxamide, and 6'-(R)-6'-C-methylneplanocin A against several ortho- and paramyxoviruses

A. Matsuda, M. Baba, M. Ito, 1992, Antimicrobial Agents and Chemotherapy.

Synthesis and optical properties, including fluorosolvatochromic and ICT-based proton-sensing behaviors of a series of 2,4,6-tris(5-aryl-2-thienyl)pyridines

S. Ogawa, H. Muraoka, T. Obara, 2019, Phosphorus, Sulfur, and Silicon and the Related Elements.

Systematic synthesis, comparative studies of the optical properties, and the ICT-based sensor properties of a series of 2,4,6-tri(5-aryl-2-thienyl)pyrimidines with the D–π–A system

S. Ogawa, H. Muraoka, T. Obara, 2016 .

Dehydrooligopeptides. X. Useful Synthetic Method for (E)- and (Z)-Isomers of Dehydroaspartic Acids, and Their Δ1,2-Dehydrodipeptides by the Base-Catalyzed β-Elimination

S. Morita, T. Obara, C. Shin, 1988 .

Dehydrooligopeptides. VIII. Convenient Syntheses of Various Dehydrotyrosine Derivatives Protected with Useful N, O-Protecting Groups via N-Carboxy Dehydrotyrosine Anhydrides

H. Nishio, T. Obara, C. Shin, 1988 .

Convenient syntheses and reactions of two kinds of basic α-dehydroamino acid derivatives

T. Obara, C. Shin, Y. Yonezawa, 1987 .

Dehydrooligopeptides. XI. Facile Syntheses of Various Kinds of Dehydrodi- and tripeptides, and Dehydroenkephalins Containing ΔTyr Residue by Using N-Carboxydehydrotyrosine Anhydride

T. Obara, C. Shin, Y. Yonezawa, 1989 .

New neplanocin analogues. 6. Synthesis and potent antiviral activity of 6'-homoneplanocin A1.

E. De Clercq, S. Shuto, R. Snoeck, 1996, Journal of medicinal chemistry.

New Neplanocin Analogues II. Enzymatic One-Step Synthesis and Antitumor Activity of 6′-(3-sn-Phosphatidyl)Neplanocin a Derivatives

S. Shuto, A. Matsuda, Tetsu Saito, 1992 .

New neplanocin analogues. 7. Synthesis and antiviral activity of 2-halo derivatives of neplanocin A.

E. De Clercq, S. Shuto, A. Matsuda, 1996, Journal of medicinal chemistry.

New neplanocin analogues. 1. Synthesis of 6'-modified neplanocin A derivatives as broad-spectrum antiviral agents.

E. De Clercq, S. Shuto, M. Hosoya, 1992, Journal of medicinal chemistry.

New neplanocin analogues. VIII. Synthesis and biological activity of 6'-C-ethyl, -ethenyl, and -ethynyl derivatives of neplanocin A.

E. De Clercq, S. Shuto, A. Matsuda, 1997, Chemical & pharmaceutical bulletin.

New neplanocin analogues. IX. A practical preparation of (6'R)-6'-C-methylneplanocin A (RMNPA), a potent antiviral agent, and the determination of its 6'-configuration. Diastereoselective deamination by adenosine deaminase.

S. Shuto, A. Matsuda, S. Yaginuma, 1997, Chemical & pharmaceutical bulletin.

New Neplanocin Analogues. V. A Potent Adenosylhomocysteine Hydrolase Inhibitor Lacking Antiviral Activity. Synthesis And Antiviral Activity Of 6″-Carboxylic Acid Derivatives Of Neplanocin A 1

A. Matsuda, S. Shigeta, S. Yaginuma, 1996 .

New neplanocin analogues. IV. 2-Fluoroneplanocin A: an adenosine deaminase-resistant equivalent of neplanocin A.

S. Shuto, A. Matsuda, S. Shigeta, 1994, Chemical & pharmaceutical bulletin.

New neplanocin analogues. III: 6'R-configuration is essential for the antiviral activity of 6'-C-methyl-3-deazaneplanocin A's

S. Shuto, A. Matsuda, S. Shigeta, 1994 .