K. Hemmi

发表

4-Azabicyclo [5, 2, 2] undeca-8, 10-dien-3-ones. Photochemical Formations and Novel Rearrangements

O. Yonemitsu, H. Nakai, K. Hemmi, 1972 .

Slow ring-inversion of the nine-membered lactam in 4-azabicyclo[5,2,2]-undeca-8,10-dien-3-one systems

O. Yonemitsu, S. Naruto, H. Nakai, 1972 .

PAF inhibitory activity of diketopiperazines: Structure-activity relationships

Keizo Yoshida, M. Hashimoto, M. Okamoto, 1991, Lipids.

Photocyclization of N-Chloroacetyl-3-methoxyphenethylamine and N-Chloroacetyl-3,5-dimethoxyphenethylamine.

O. Yonemitsu, Y. Okuno, K. Hemmi, 1972 .

Transannular formation of 1,10-dimethoxy-4-azatricyclo[6,2,2,04,8]dodeca-9,11-dien-3-one

O. Yonemitsu, Y. Okuno, K. Hemmi, 1971 .

New mechanism-based serine protease inhibitors: inhibition of human leukocyte elastase, porcine pancreatic elastase, human leukocyte cathepsin G, and chymotrypsin by 3-chloroisocoumarin and 3,3-dichlorophthalide

J. Harper, J. Powers, K. Hemmi, 1983 .

Studies on phosphonic acid antibiotics. IV. Synthesis and antibacterial activity of analogs of 3-(N-acetyl-N-hydroxyamino)-propylphosphonic acid (FR-900098).

M. Hashimoto, T. Kamiya, K. Hemmi, 1982, Chemical & pharmaceutical bulletin.

SYNTHESIS OF OPTICALLY ACTIVE β-METHYLTRYPTOPHANS FROM AZIRIDINE-2-CARBOXYLATES

M. Hashimoto, K. Imai, N. Shimazaki, 1990 .

FLASH PHOTOLYSIS OF ALLYL PHENYL ETHERS

O. Yonemitsu, S. Naruto, K. Hirao, 1974 .

EXCIPLEXES AND CAGE COMPLEXES IN THE PHOTOLYSIS OF N‐CHLOROACETYLMESCALINE AND OTHER PHENETHYLAMINES

B. Witkop, O. Yonemitsu, S. Naruto, 1972, Photochemistry and photobiology.

Studies on Phosphonic Acid Antibiotics. III. Structure and Synthesis of 3-(N-Acetyl-N-hydroxyamino) propylphosphonic Acid (FR-900098) and 3-(N-Acetyl-N-hydroxyamino)-2 (R)-hydroxypropyl-phosphonic Acid (FR-33289)

M. Hashimoto, T. Kamiya, K. Hemmi, 1981 .

Studies on phosphonic acid antibiotics. II. Synthesis of 3-(n-acetyl-n-hydroxyamino)-2(r)-hydroxypropylphosphonic acid (FR-33289) and 3-(n-formyl-n-hydroxyamino)-1-trans-propenylphosphonic acid (FR-32863)

M. Hashimoto, T. Kamiya, K. Hemmi, 1980 .

Studies on phosphonic acid antibiotics. I. Structure and synthesis of 3-(n-acetyl-n-hydroxyamino)propylphosphonic acid (FR-900098) and its n-formyl analogue (FR-31564)

M. Hashimoto, T. Kamiya, K. Hemmi, 1980 .

M. Hashimoto, K. Hemmi, Kamiya Takashi, 1980 .

Studies on structure-activity relationships of FK-156, an immunostimulating peptide, and related compounds. I. Synthesis of stereoisomeric analogues of FK-156.

S. Okada, M. Hashimoto, Y. Kitaura, 1984, Chemical & pharmaceutical bulletin.

Synthesis and antibacterial activity of new 1-oxa-1-dethiacephalosporins.

M. Hashimoto, D. Hagiwara, M. Aratani, 1980, Journal of medicinal chemistry.

WF-10129, a novel angiotensin converting enzyme inhibitor produced by a fungus, Doratomyces putredinis.

M. Okuhara, A. Fujie, Y. Tsurumi, 1987, The Journal of antibiotics.

Reaction of serine proteases with substituted isocoumarins: discovery of 3,4-dichloroisocoumarin, a new general mechanism based serine protease inhibitor.

J. Harper, J. Powers, K. Hemmi, 1985, Biochemistry.

Diketopiperazine derivatives, a new series of platelet-activating factor inhibitors.

M. Hashimoto, I. Shima, N. Shimazaki, 1987, Chemical & pharmaceutical bulletin.

WA8242A1, A2 and B, novel secretary phospholipase A2 inhibitors produced by Streptomyces violaceusniger. III. Structure elucidation and total synthesis of WA8242B.

S. Okada, M. Okamoto, S. Yoshimura, 1998, The Journal of antibiotics.

TRANSANNULARE BLDG. VON 1,10-DIMETHOXY-4-AZA-TRICYCLO(6,2,2,0(4,8))DODECA-9,11-DIEN-3-ON

O. Yonemitsu, Y. Okuno, K. Hemmi, 1971 .

PHOTOCYCLISIERUNG VON N-CHLORACETYL-3-METHOXYPHENAETHYLAMIN UND N-CHLORACETYL-3,5-DIMETHOXYPHENAETHYLAMIN

O. Yonemitsu, Y. Okuno, K. Hemmi, 1972 .

Studies on a new immunoactive peptide, FK-156. IV. Synthesis of FK-156 and its geometric isomer.

Y. Miyazaki, S. Okada, M. Hashimoto, 1982, The Journal of antibiotics.

TOTAL SYNTHESIS OF FK‐156 ISOLATED FROM A STREPTOMYCES AS AN IMMUNOSTIMULATING PEPTIDE: APPLICATION OF A NOVEL COPPER CHELATE AMINO PROTECTION

S. Okada, M. Hashimoto, Y. Kitaura, 1982 .

Studies on structure-activity relationships of FK-156, an immunostimulating peptide, and related compounds. II. Synthesis of N2-(gamma-D-glutamyl)-2(L), 2'(D)-diaminopimelic acid as the minimal essential structure of FK-156.

S. Okada, M. Hashimoto, Y. Kitaura, 1984, Chemical & pharmaceutical bulletin.

Synthesis and immunostimulating activity of FK-156 analogues: fatty acid derivatives of N-[N alpha-(gamma-D-glutamyl)-L-lysyl]-D-alanine.

S. Okada, M. Hashimoto, Y. Mine, 1982, Chemical & pharmaceutical bulletin.

Total synthesis of FK-156 isolated from a Streptomyces as an immunostimulating peptide: application of a novel copper chelate amino protection

S. Okada, M. Hashimoto, Y. Kitaura, 1981 .

Synthesis and characterization of orally active nonpeptide vasopressin V2 receptor antagonists.

H. Tanaka, N. Hosogai, M. Tomita, 1999, Chemical and pharmaceutical bulletin.

Synsthesis and RES-stimulating activity of bacterial cell-wall peptidoglycan peptides related to FK-156

S. Okada, M. Hashimoto, Y. Kitaura, 1982, Experientia.

Diketopiperazines as a new class of platelet-activating factor inhibitors.

M. Hashimoto, I. Shima, N. Shimazaki, 1987, Journal of medicinal chemistry.

PAF inhibitors of microbial origin. Studies on diketopiperazine derivatives.

M. Okamoto, K. Yoshida, N. Shimazaki, 1988, Progress in biochemical pharmacology.

Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin A alpha, and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones.

J. Harper, J. Powers, K. Hemmi, 1985, Biochemistry.

The physiological roles of membrane ergosterol as revealed by the phenotypes of syr1/erg3 null mutant of Saccharomyces cerevisiae.

D. Hirata, E. Tsuchiya, T. Miyakawa, 1995, Bioscience, biotechnology and biochemistry.

TOTAL SYNTHESIS OF UROGASTRONE (HUMAN EPIDERMAL GROWTH FACTOR, H‐EGF)

Y. Miyazaki, M. Neya, M. Hashimoto, 1985 .

Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 1. Synthesis of the fully protected urogastrone

Y. Miyazaki, M. Neya, M. Hashimoto, 1989 .