M. Fuji

发表

Carbamoyl pyridone HIV-1 integrase inhibitors. 1. Molecular design and establishment of an advanced two-metal binding pharmacophore.

T. Seki, T. Fujiwara, T. Yoshinaga, 2012, Journal of medicinal chemistry.

sckl, a High Copy Number Suppressor of Defects in the CAMP-Dependent Protein Kinase Pathway in Fission Yeast, Encodes a Protein Homologous to the Saccharomyces cer&ae SCH9 Kinase

C. S. Hoffman, M. Fuji, Mei, 2002 .

A Stereoselective and Highly Practical Synthesis of Cytosolic Phospholipase A2 Substrate, 2‐S‐Arachidonoyl‐1‐O‐hexadecyl‐sn‐2‐thioglycero‐3‐O‐phosphocholine.

H. Hashizume, Y. Fujii, M. Fuji, 1998 .

A STEREOSELECTIVE AND HIGHLY PRACTICAL SYNTHESIS OF CYTOSOLIC PHOSPHOLIPASE A2 SUBSTRATE, 2-S-ARACHIDONOYL-1-O-HEXADECYL-SN-2-THIOGLYCERO-3-O-PHOSPHOC HOLINE

H. Hashizume, Y. Fujii, M. Fuji, 1997 .

Carbamoyl pyridone HIV-1 integrase inhibitors. 2. Bi- and tricyclic derivatives result in superior antiviral and pharmacokinetic profiles.

E. Garvey, T. Seki, T. Fujiwara, 2013, Journal of medicinal chemistry.

Total Synthesis of Terprenin, a Novel Immunosuppressive p-Terphenyl Derivative.

T. Nakatani, K. Kawada, S. Yonezawa, 1998, The Journal of organic chemistry.

3-Hydroxy-1,5-dihydro-pyrrol-2-one derivatives as advanced inhibitors of HIV integrase.

T. Fujiwara, T. Yoshinaga, R. Kiyama, 2007, Bioorganic & medicinal chemistry.

3‐Hydroxy‐1,5‐dihydro‐pyrrol‐2‐one Derivatives (IV) as Advanced Inhibitors of HIV Integrase.

T. Fujiwara, T. Yoshinaga, R. Kiyama, 2007 .

A platform for designing HIV integrase inhibitors. Part 2: a two-metal binding model as a potential mechanism of HIV integrase inhibitors.

Akihiko Sato, T. Fujiwara, T. Yoshinaga, 2006, Bioorganic & medicinal chemistry.

Highly selective and orally active inhibitors of type IV collagenase (MMP-9 and MMP-2): N-sulfonylamino acid derivatives.

H. Tsuzuki, T. Nakatani, K. Sugita, 1998, Journal of medicinal chemistry.

Asymmetric Synthesis Using Chiral Acetals : Highly Diastereoselective Addition of Organocerium Reagents to Chiral α-Aldoxime-Ether Acetal

Y. Kita, H. Annoura, H. Fujioka, 1989 .

Asymmetric synthesis using chiral acetals. Studies on the nucleophilic addition of organometallics to chiral .ALPHA.-keto acetals in open-chain systems.

H. Annoura, H. Fujioka, Y. Tamura, 1987 .

Asymmetric synthesis using chiral acetals: Studies on the nucleophilic addition of organometallics to chiral x-keto acetals in cyclic systems.

H. Annoura, H. Fujioka, Y. Tamura, 1987 .

Diastereoselective nucleophilic addition to chiral open-chain α-ketoacetals: Synthesis of (R)- and (S)-mevalolactone

H. Annoura, H. Fujioka, Y. Tamura, 1986 .

The Transition Metal-Catalyzed Intermolecular [5+2] Cycloaddition: The Homologous Diels−Alder Reaction

P. Wender, H. Rieck, M. Fuji, 1998 .

Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 6. Synthetic Procedure for 4-, 5-, 6-, or 7-Alkoxy- and Hydroxyindole Derivatives

H. Muratake, M. Fuji, M. Natsume, 1992 .

Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 7. Synthesis of (±)- and (S)-(-)-Pindolol

H. Muratake, M. Fuji, M. Natsume, 1992 .

Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 9.Synthesis of (1aS, 8bS)-1-tert-Butyloxycarbonyl-8-formyl-1,1a, 2,8b-tetrahydroazirino[2', 3' : 3,4]pyrrolo[1,2-α]indole. Model Study for the Enantiospecific Synthesis of Aziridinomitosenes

Tomohiro Sato, I. Utsunomiya, M. Fuji, 1993 .

Preparation of Alkyl-Substituted Indoles in the Bezene Portion. Part 5. Efficient Preparative Procedure for 4-Substituted Indole Derivatives

H. Muratake, M. Fuji, Mitsutake Matsume, 1992 .

Synthesis and antiviral activity of 7-benzyl-4-hydroxy-1,5-naphthyridin-2(1H)-one HIV integrase inhibitors.

E. Garvey, S. Foster, T. Fujiwara, 2009, Journal of medicinal chemistry.

Total Synthesis of Terprenin, a Highly Potent and Novel Immunoglobulin E Antibody Suppressant.

T. Nakatani, K. Kawada, S. Yonezawa, 1998, Angewandte Chemie.

Carbamoyl pyridone HIV-1 integrase inhibitors 3. A diastereomeric approach to chiral nonracemic tricyclic ring systems and the discovery of dolutegravir (S/GSK1349572) and (S/GSK1265744).

E. Garvey, T. Seki, S. Foster, 2013, Journal of medicinal chemistry.

Rhodium-Catalyzed [5 + 2] Cycloadditions of Allenes and Vinylcyclopropanes: Asymmetric Total Synthesis of (+)-Dictamnol.

P. Wender, J. Love, Craig O. Husfeld, 1999 .