H. Moriyama

发表

High temperature treatment of polyfurfuryl alcohol/graphite oxide intercalation compound

T. Kyotani, A. Tomita, H. Moriyama, 1997 .

Drug design, synthesis, and evaluation of a non-sugar-based selectin antagonist.

H. Kondo, H. Moriyama, K. Fukunaga, 2001, Bioorganic & medicinal chemistry letters.

Versatile synthesis of oligosaccharide-containing fullerenes

K. Niikura, F. Feng, S. Nishimura, 2005 .

Synthesis and biological activity of selective azasugar-based TACE inhibitors.

S. Nishimura, H. Kondo, Y. Inoue, 2004, Bioorganic & medicinal chemistry letters.

Structure--activity relationships of azasugar-based MMP/ADAM inhibitors.

S. Nishimura, H. Kondo, Y. Inoue, 2003, Bioorganic & medicinal chemistry letters.

Design, synthesis and evaluation of novel azasugar-based MMP/ADAM inhibitors.

S. Nishimura, H. Kondo, Y. Inoue, 2003, Bioorganic & medicinal chemistry letters.

Structural effect of cobalt Schiff base complex catalyst on its catalytic activity in dioxygenolysis of 3-methylindole

Y. Fujii, A. Nishinaga, T. Mashino, 1993 .

Azasugar-based MMP/ADAM inhibitors as antipsoriatic agents.

S. Nishimura, H. Kondo, Y. Inoue, 2004, Journal of medicinal chemistry.

PREPARATION OF BICYCLIC GUANIDINES BY THE IODOCYCLIZATION OF 3-ALKENYL-2-(SUBSTITUTED AMINO)- 1-IMIDAZOLIN-4-ONES1

A. Kakehi,, H. Okada, H. Moriyama, 1996 .

Stereoselective synthesis of the C-4 linked imidazole nucleosides using modified Mitsunobu reaction

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1).

S. Harusawa, H. Ohishi, T. Kurihara, 1996, The Journal of organic chemistry.

Efficient and β-Stereoselective Synthesis of 4(5)-(β-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles.

S. Harusawa, H. Ohishi, H. Moriyama, 2010 .

Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5-amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity

S. Harusawa, H. Ohishi, T. Kurihara, 1997 .

Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5- amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity.

S. Harusawa, H. Ohishi, T. Kurihara, 1997 .

Studies on selection blockers. 5. Design, synthesis, and biological profile of sialyl Lewis x mimetics based on modified serine-glutamic acid dipeptides.

H. Kondo, H. Ohmoto, T. Saito, 1997, Journal of medicinal chemistry.

[3,3]sigmatropic ring expansion of cyclic thionocarbonates. 13.1 synthesis of medium-membered heterocyclic allenes and synthetic application to antifungal constitutent of Sapium japonicum

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates. Part 13. Synthesis of Medium-Membered Heterocyclic Allenes and Synthetic Application to Antifungal Constituent of Sapium japonicum.

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

Studies on selectin blockers. 6. Discovery of homologous fucose sugar unit necessary for E-selectin binding.

H. Kondo, Y. Inoue, Y. Hiramatsu, 1998, Journal of medicinal chemistry.

Studies on selectin blocker. 9. SARs of non-sugar selectin blocker against E-, P-, L-selectin bindings.

H. Kondo, Y. Inoue, Y. Hiramatsu, 2001, Bioorganic & medicinal chemistry.

Studies on selectin blockers. 7. Structure-activity relationships of sialyl Lewis X mimetics based on modified Ser-Glu dipeptides.

H. Kondo, Y. Inoue, K. Kurokawa, 1998, Journal of medicinal chemistry.