T. Kubota

发表

The 7α-methoxy substituent in cephem or oxacephem antibiotics enhances in vivo anti-Helicobacter felis activity in mice after oral administration

Yoshinao Kobayashi, K. Murakami, H. Nagata, 2000 .

ORALLY ACTIVE CEPHALOSPORINS

M. Kume, Y. Kimura, M. Nakano, 1993 .

Orally Active Cephalosporins. Part 1. Synthesis and Structure‐Activity Relationships of 7β‐(2‐(R)‐Amino‐2‐phenylacetamido)‐3‐(1H‐1,2,3‐ triazol‐4‐yl)alkylthiomethyl ‐3‐cephem‐4‐carboxylic Acid and Related Compounds

M. Kume, Y. Kimura, K. Motokawa, 1993 .

Orally active cephalosporins. III. Synthesis and structure-activity relationships of new 3-heterocyclicthiomethylthio-7 beta-[(Z)- 2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-3-cephem-4 -carboxylic acids.

M. Kume, Y. Kimura, K. Motokawa, 1993, The Journal of antibiotics.

Synthesis and biological properties of 7 beta-[(Z)-2-(2-amino-4-thiazolyl)-4-carboxy-2-butenoylamino]-3-cephem- 4-carboxylic acid (7432-S), a new oral cephem antibiotic.

Y. Hamashima, T. Yoshida, T. Konoike, 1987, The Journal of antibiotics.

Intramolecular Carbenoid Reactions of Pyrrole Derivatives. A Total Synthesis of (±)‐Ipalbidine

C. W. Jefford, T. Kubota, A. Zaslona, 1986 .

Novel and efficient synthesis of 1β-methylcarbapenems utilizing cyclization of hypervalent iodonium ylides

Y. Iso, M. Kume, T. Kubota, 1995 .

Organic photochemical reactions. XXIV. Photocycloaddition of propanal to 1,3-cyclohexadiene.

K. Shima, H. Sakurai, T. Kubota, 1976 .

THE PHOTOADDITION OF STILBENE TO 1-METHYLPYRROLE. THE EFFECT OF PROTIC SOLVENTS

H. Sakurai, T. Kubota, 1972 .

New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 3: 7beta-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetamido] cephalosporins bearing 4-[3-(aminoalkyl)-ureido]-1-pyridinium a

H. Yoshizawa, H. Miwa, K. Minami, 2004, Bioorganic & medicinal chemistry.

New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 2: Synthesis and structure-activity relationships in the S-3578 series.

H. Ishitobi, H. Yoshizawa, H. Miwa, 2004, Bioorganic & medicinal chemistry.

S-3578, a new broad spectrum parenteral cephalosporin exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Synthesis and structure-activity relationships.

T. Iwaki, H. Yoshizawa, T. Irie, 2002, The Journal of antibiotics.

Orally active cephalosporins. II. Synthesis and structure-activity relationships of new 7 beta-[(Z)-2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-cephalospori ns with 1,2,3-triazole in C-3 side chain.

M. Kume, Y. Kimura, M. Nakano, 1993, The Journal of antibiotics.

Photocycloaddition of diphenylacetylene to 1,5-cyclooctadiene

H. Sakurai, T. Kubota, 1973 .

Synthetic studies on .beta.-lactam antibiotics. 12. Stereocontrolled synthesis of 7.alpha.-methoxy-1-oxacephems from 6-epipenicillin G

Y. Hamashima, K. Okada, S. Uyeo, 1979 .

Synthetic studies on β-lactam antibiotics. 15. conversion of 7-epicephems into 1-oxacephems

Y. Hamashima, W. Nagata, T. Kubota, 1980 .