World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
46
Citations
7047
World Ranking
16125
National Ranking
1273

Overview

Masaji Ohno is affiliated with the University of Tokyo in Japan. Their academic profile reflects a career connected to this institution, although specific details on individual research contributions or fields of specialization are not documented in the available data.

There are no listed recent papers, co-authors, publication venues, or book publications attributed to Masaji Ohno in the provided information. Similarly, no details are available regarding their main fields of study, subfields, or primary topics of research.

Information about awards or recognitions received by Masaji Ohno is also not included, providing no indication of distinctions or honors in their academic career.

Due to the limited data, a comprehensive overview of this scientist's research output, thematic focus, and collaborations cannot be elaborated beyond their established affiliation with the University of Tokyo.

Best Publications

  • Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric induction

    Yi Fong Wang;Toshio Izawa;Susumu Kobayashi;Masaji Ohno

  • A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: Alkylation of aldehydes catalyzed by disulfonamide-Ti(O-i-Pr)4-Dialkyl zinc system

    Hideyo Takahashi;Takashi Kawakita;Masaji Ohno;Masato Yoshioka

  • Asymmetric induction catalyzed by conjugate bases of chiral proton acids as ligands: Enantioselective addition of dialkylzinc-orthotitanate complex to benzaldehyde with catalytic ability of a remarkable high order

    Masato Yoshioka;Takashi Kawakita;Masaji Ohno

  • Enantioselective synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)-neplanocin A by a chemicoenzymatic approach

    Masafumi Arita;Kunitomo Adachi;Yukishige Ito;Hiroaki Sawai

  • Enantioselective alkylation of aldehyde catalyzed by disulfonamide-Ti(O-i-Pr)4-dialkyl zinc system

    Hideyo Takahashi;Takashi Kawakita;Masato Yoshioka;Susumu Kobayashi

  • Total Synthesis of Longifolene

    E. J. Corey;Masaji. Ohno;Rajat B. Mitra;Paul A. Vatakencherry

  • Ph3P-(PyS)2-CH3CN as an excellent condensing system for .beta.-lactam formation from .beta.-amino acids

    Susumu Kobayashi;Takamasa Iimori;Toshio Izawa;Masaji Ohno

  • Man-designed bleomycin with altered sequence specificity in DNA cleavage

    Masami Otsuka;Takeshi Masuda;Andreas Haupt;Masaji Ohno

  • SYNTHESIS OF (S)- AND (R)-4((METHOXYCARBONYL)METHYL)-2-AZETIDINONE BY CHEMICOENZYMIC APPROACH

    Masaji Ohno;Susumu Kobayashi;Takamasa Iimori;Yi-Fong Wang

  • Negamycin, a novel hydrazide antibiotic.

    Shinichi Kondo;Seiji Shibahara;Shuji Takahashi;Kenji Maeda

  • Structure of coformycin, an unusual nucleoside of microbial origin.

    Unknown

  • Creation of novel chiral synthons with enzymes and applications to natural product synthesis. 15. Efficient introduction of chiral centers into cyclohexane ring

    Susumu Kobayashi;Keiji Kamiyama;Takamasa Iimori;Masaji Ohno

  • An Efficient O-Monoalkylation of Dimethyl L-Tartrate via O-Stannylene Acetal with Alkyl Halides in the Presence of Cesium Fluoride

    Nobuo Nagashima;Masaji Ohno

  • Total syntheses of negamycin and the antipode

    Seiji Shibahara;Shinichi Kondo;Kenji Maeda;Hamao Umezawa

  • Synthetic analogues and biosynthetic intermediates of bleomycin. Metal-binding, dioxygen interaction, and implication for the role of functional groups in bleomycin action mechanism.

    Y Sugiura;T Suzuki;M Otsuka;S Kobayashi

  • CHIRALLY SELECTIVE SYNTHESIS OF SUGAR MOIETY OF NUCLEOSIDES BY CHEMICOENZYMATIC APPROACH: L- AND D-RIBOSES, SHOWDOMYCIN, AND CORDYCEPIN

    Y. Ito;T. Shibata;M. Arita;H. Sawai

  • Total synthesis of bleomycin A21)

    Tomohisa Takita;Yoji Umezawa;Sei ichi Saito;Hajime Morishima

  • A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: Simmons-Smith cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system

    Hideyo Takahashi;Masato Yoshioka;Masakatsu Shibasaki;Masaji Ohno

  • Selective Monoalkylation of Acyclic Diols by Means of Dibutyltin Oxide and Fluoride Salts.

    Nobuo Nagashima;Masaji Ohno

  • A stereocontrolled synthesis of (−)-bestatin from an acyclic allylamine by iodocyclocarbamation

    Susumu Kobayashi;Toshiyuki Isobe;Masaji Ohno

  • Synthetic studies on biologically active natural products by a chemicoenzymatic approach: Enantioselective synthesis of C- and N-nucleosides, showdomycin, 6-azapseudouridine and cordycepin

    Masaji Ohno;Yukishige Ito;Masafumi Arita;Tomoyuki Shibata

  • A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system

    Unknown

Frequent Co-Authors

Hamao Umezawa
Hamao Umezawa National Institutes of Health
Yukio Sugiura
Yukio Sugiura Kyoto University
Keizo Inoue
Keizo Inoue University of Tokyo
Yoshio Takahashi
Yoshio Takahashi University of Tokyo
Masakatsu Shibasaki
Masakatsu Shibasaki University of Tokyo
Tomio Takeuchi
Tomio Takeuchi Keio University
Hiroshi Naganawa
Hiroshi Naganawa Keio University
Yoichi Iitaka
Yoichi Iitaka University of Tokyo
Masa Hamada
Masa Hamada Keio University

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