K. Mori

发表

Intracellular inducible alkylation system that exhibits antisense effects with greater potency and selectivity than the natural oligonucleotide.

K. Kataoka, F. Nagatsugi, Y. Nagasaki, 2006, Angewandte Chemie.

Phosphoroselenoate oligodeoxynucleotides: synthesis, physico-chemical characterization, anti-sense inhibitory properties and anti-HIV activity.

J. Toulmé, S. Broder, C. Stein, 1989, Nucleic acids research.

Oligodeoxynucleotide analogs with 5′‐linked anthraquinone

J. S. Cohen, C. Subasinghe, K. Mori, 1989, FEBS letters.

Magnetic circular dichroism and fluorescence spectra of 5-deazaflavins

F. Yoneda, A. Koshiro, H. Yamaguchi, 1981 .

A novel synthesis of pyrimido[4,5-b]quinoline-2(3H),4(10H)-diones (5-deazaflavins) and analogues by the oxidative cyclization of 5,5′-arylmethylenebis-(6-alkylamino-3-methyluracils)

F. Yoneda, H. Yamaguchi, K. Mori, 1980 .

Synthesis of some 8-substituted 5-deazaflavins

F. Yoneda, A. Koshiro, K. Mori, 1982 .

Dehydrogenation of alcohols by pyrimido[4,5-b]quinoline-2(3H),4(10H)-diones (5-deazaflavins) as autorecycling oxidizing agents

F. Yoneda, K. Mori, Y. Sakuma, 1981 .

Synthesis and Properties of Novel 5′-Linked Oligos

J. S. Cohen, C. Stein, C. Subasinghe, 1989 .

Synthesis and anti-HIV-1 activity of novel 10-thiaisoalloxazines, a structural analog of C-5 and/or C-6 substituted pyrimidine acyclonucleoside.

K. Shinozuka, M. Baba, S. Shigeta, 2003, Chemical & pharmaceutical bulletin.

Facile Synthesis of a Phosphotriester Intermediates for Solution-Phase Preparation of Oligonucleotide Phosphorothioates.

K. Shinozuka, K. Mori, T. Miyashita, 1999 .

Syntheses of 2-Deoxo-2-phenyl-5-deazaflavins and 3-Phenyl-5-deazaflavins and Their Use in the Oxidation of Benzyl Alcohol and Benzylamine

F. Yoneda, K. Mori, M. Ono, 1980 .

Investigation of a Facile Synthetic Method for Phosphorothioate Dimer Synthons In Oligonucleotide Phosphorothioates Synthesis

K. Shinozuka, K. Kondo, Kohei Yamada, 2000, Nucleosides, nucleotides & nucleic acids.