H. Itazaki

发表

Isolation and structural elucidation of new cyclotetrapeptides, trapoxins A and B, having detransformation activities as antitumor agents.

H. Itazaki, K. Nagashima, K. Sugita, 1990, The Journal of antibiotics.

Cinatrins, a novel family of phospholipase A2 inhibitors. I. Taxonomy and fermentation of the producing culture; isolation and structures of cinatrins.

H. Itazaki, K. Nagashima, Y. Kawamura, 1992, The Journal of antibiotics.

Angular-Substituted Polycyclic Compounds. I. Cyanation of Δ4-Cholesten-3-one

H. Itazaki, W. Nagata, K. Takeda, 1961 .

Synthetic Studies on Isoquinoline Alkaloids. I. An Efficient Synthesis of 9, 10-Substituted Protoberberine Alkaloids

H. Itazaki, W. Nagata, T. Wakabayashi, 1975 .

The structure of PA48009: the revised structure of duramycin.

H. Itazaki, K. Nagashima, Y. Kawamura, 1990, The Journal of antibiotics.

Cinatrins, a novel family of phospholipase A2 inhibitors. II. Biological activities.

K. Tanaka, H. Itazaki, T. Yoshida, 1992, The Journal of antibiotics.

Synthesis of 2,3-dihydro-1,4-benzodioxin derivatives. II. 5(or 6)-acyl 2,3-dihydro-1,4-benzodioxin derivatives: new phenoxyacetic acid diuretics.

H. Itazaki, M. Nakamura, Y. Yonetani, 1988, Chemical & pharmaceutical bulletin.

Synthetic studies on isoquinoline alkaloids. II. Selective conversion of 3,9,10-substituted tetrahydroprotoberberines into 3,9,10-substituted 5,6,7,8,13,14-hexahydrodibenz(c,g)azecines.

H. Itazaki, W. Nagata, K. Okada, 1975 .

SYNTHETIC STUDIES ON ISOQUINOLINE ALKALOIDS. II. SELECTIVE CONVERSION OF 3,9,10-SUBSTITUTED TETRAHYDROPROTOBERBERINES INTO 3,9,10-SUBSTITUTED 14-DEOXOPROTOPINES. TOTAL SYNTHESIS OF 3,9,10-SUBSTITUTED 5,6,7,8,13,14-HEXAHYDRODIBENZ(C,G)

H. Itazaki, W. Nagata, K. Okada, 1976 .

Nuclear Magnetic Resonance Spectroscopic Evidence for Distorted Conformations of the C-Rings in 8β, 11β- and 11β, 13β-Bridged Steroids

H. Itazaki, W. Nagata, K. Tori, 1963 .

NOVEL FAMILY OF PHOSPHOLIPASE A 2 INHIBITORS II . BIOLOGICAL ACTIVITIES

H. Itazaki, Tadashi Yoshida, Kazushige Tanaka, 2006 .

Salfredins, new aldose reductase inhibitors produced by Crucibulum sp. RF-3817. I. Fermentation, isolation and structures of salfredins.

H. Itazaki, K. Nagashima, Y. Kawamura, 1995, The Journal of antibiotics.