Updated on 2025/11/26

写真a

 
ANDO YOSHIO
 
Organization
School of Science Associate Professor
Title
Associate Professor
External link

Degree

  • Ph. D. ( 2007.3   Tokyo Institute of Technology )

Research Interests

  • Synthetic Organic Chemistry, Natural Product Synthesis, Asymmetric Synthesis, Photochemical Reaction

Research Areas

  • Life Science / Bioorganic chemistry  / Natural Product Synthesis

  • Nanotechnology/Materials / Synthetic organic chemistry

Education

  • Tokyo Institute of Technology   Graduate School of Science and Engineering   Department of Applied Chemistry

    2002.4 - 2007.3

      More details

    Country: Japan

    researchmap

  • Tokyo Institute of Technology   School of Engineering   Department of Applied Chemistry

    1998.4 - 2002.3

      More details

    Country: Japan

    researchmap

Research History

  • Institute of Science Tokyo   Department of Chemistry   Associate Professor

    2024.10

      More details

    Country:Japan

    researchmap

  • Tokyo Institute of Technology   Department of Chemistry   Associate Professor

    2024.6 - 2024.9

      More details

    Country:Japan

    researchmap

  • Tokyo Institute of Technology   Department of Chemistry   Assistant Professor

    2016.4 - 2024.5

      More details

    Country:Japan

    researchmap

  • Tokyo Institute of Technology   Department of Chemistry   Assistant Professor

    2008.9 - 2016.3

      More details

    Country:Japan

    researchmap

  • The Scripps Research Institute

    2007.5 - 2008.8

      More details

    Country:United States

    researchmap

Professional Memberships

  • The Society of Synthetic Organic Chemistry, Japan

    2004

      More details

  • The Japanese Society of Carbohydrate Research

    2002

      More details

  • The Chemical Society of Japan

    2002

      More details

Papers

  • Proximity-induced chirality at the achiral conductive interface by electrical control of enantiopure ion adsorption

    Yoshio Ando, Toshiya Ideue, Po-Jung Huang, Kouji Taniguchi, Miuko Tanaka, Yukito Nishio

    Science Advances   2025.11

     More details

    Publishing type:Research paper (scientific journal)  

    DOI: 10.1126/sciadv.adx2281

    researchmap

  • Synthetic study on γ-rubromycin: spiroacetal formation by using photochemical reaction of 2-hydroxy-1,4-naphthoquinone Reviewed

    Yoshio Ando, Daichi Ogawa, Shuichiro Morishita, Keisuke Suzuki, Ken Ohmori

    Chemistry Letters   54 ( 11 )   upaf186   2025.10

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Oxford University Press (OUP)  

    Abstract

    The photochemical reaction of 2-hydroxy-1,4-naphthoquinone gives [5,6]-spiroacetal structure, a partial structure in γ-rubromycin. The viability of the reaction depended on the number of methoxy substituents on the naphthoquinone moiety, and the substrate tolerance has been studied.

    DOI: 10.1093/chemle/upaf186

    researchmap

    Other Link: https://academic.oup.com/chemlett/article-pdf/54/11/upaf186/64632733/upaf186.pdf

  • Synthetic Study on Bicyclic Pyranonaphthoquinone Natural Products: Construction of the Dioxabicyclo[3.3.1]nonene Motif Reviewed

    Yoshio Ando, Sota Ajima, Ken Ohmori

    ChemistryEurope   3   e202500086   2025.7

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/ceur.202500086

    researchmap

  • Total Syntheses of β‐ and γ‐Naphthocyclinones Reviewed

    Yoshio Ando, Taiju Hoshino, Nozomi Tanaka, Mark M. Maturi, Yusuke Nakazawa, Takumi Fukazawa, Ken Ohmori, Keisuke Suzuki

    Angewandte Chemie International Edition   64 ( 6 )   2024.11

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    Abstract

    After half a century from their isolation in 1974, we report the first total syntheses of β‐ and γ‐naphthocyclinones, two dimeric pyranonaphthoquinones featuring an unusual bicyclo[3.2.1]octadienone core. The syntheses were achieved with full stereochemical control and functional group management, relying on 1) enantioselective construction of the bicyclic core by Rh‐catalyzed enantioselective 1,4‐addition followed by thiolate‐mediated reductive cyclization, and 2) judicious design of a common chiral, non‐racemic monomer unit that is capable of divergence into the donor and acceptor units, and reunion to construct the bicyclo[3.2.1]octadienone core.

    DOI: 10.1002/anie.202415108

    researchmap

  • Atomic-resolution structure analysis inside an adaptable porous framework Reviewed

    Yuki Wada, Pavel M. Usov, Bun Chan, Makoto Mukaida, Ken Ohmori, Yoshio Ando, Haruhiko Fuwa, Hiroyoshi Ohtsu, Masaki Kawano

    Nature Communications   15 ( 1 )   2024.1

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    Abstract

    We introduce a versatile metal-organic framework (MOF) for encapsulation and immobilization of various guests using highly ordered internal water network. The unique water-mediated entrapment mechanism is applied for structural elucidation of 14 bioactive compounds, including 3 natural product intermediates whose 3D structures are clarified. The single-crystal X-ray diffraction analysis reveals that incorporated guests are surrounded by hydrogen-bonded water networks inside the pores, which uniquely adapt to each molecule, providing clearly defined crystallographic sites. The calculations of host-solvent-guest structures show that the guests are primarily interacting with the MOF through weak dispersion forces. In contrast, the coordination and hydrogen bonds contribute less to the total stabilization energy, however, they provide highly directional point interactions, which help align the guests inside the pore.

    DOI: 10.1038/s41467-023-44401-w

    researchmap

    Other Link: https://www.nature.com/articles/s41467-023-44401-w

  • Study on Integrated Synthesis of Dimeric Pyranonaphthoquinones: Preparation of Versatile Synthetic Intermediate and Conversion into ent-Hemi-actinorhodin and ent-Hemi-γ-actinorhodin Reviewed

    Yoshio Ando, Keisuke Suzuki, Mark M. Maturi, Taiju Hoshino, Nozomi Tanaka, Takahiro Sakai, Ken Ohmori

    Synlett   2023.7

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Georg Thieme Verlag KG  

    Abstract

    For developing general synthetic access toward dimeric pyranonaphthoquinones including β-naphthocyclinone, actinorhodin, and γ-actinorhodin, we report stereodefined 6,9,10-trioxypyranonaphthalene as a versatile intermediate. Its robust preparation started from ethyl (S)-4-chloro-3-hydroxybutyrate. The pyranonaphthalene core was constructed by a Michael–Dieckmann sequence, and methylation using Me3Al and BF3·OEt2 established the required trans structure in a scalable manner. Conversion of this intermediate into ent-hemi-actinorhodin and into ent-hemi-γ-actinorhodin are also reported, in which the conditions for the oxidative lactonization were optimized.

    DOI: 10.1055/a-2124-4161

    researchmap

  • Photochemical Reaction of 1,2-Naphthoquinone toward Enantioselective Synthesis of γ-Rubromycin: Viability Dependence on Chromophore Invited Reviewed

    Yoshio Ando, Ken Ohmori, Daichi Ogawa, Fumihiro Wakita, Keisuke Suzuki

    Synlett   2023.6

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Georg Thieme Verlag KG  

    Abstract

    Aiming at the enantioselective total synthesis of γ-rubromycin, we reported the photochemical reaction of 1,2-naphthoquinone as a promising solution to otherwise-difficult enantiocontrol of the single spiroacetal stereogenic center. The present study examined the applicability of this approach to more functionalized substrates, which revealed viability dependence on the chromophore structure differing in the position and number of methoxy substituents.

    DOI: 10.1055/a-2113-0212

    researchmap

  • Stereospecific naphthoquinone photoredox reactions: Total syntheses of spirocyclic natural products Reviewed

    Yoshio Ando, Keisuke Suzuki

    Tetrahedron   139   133448 - 133448   2023.6

     More details

    Authorship:Lead author, Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Elsevier BV  

    DOI: 10.1016/j.tet.2023.133448

    researchmap

  • Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6‐Hydrogen Atom Transfer Reviewed

    Yoshio Ando, Daichi Ogawa, Ken Ohmori, Keisuke Suzuki

    Angewandte Chemie International Edition   62 ( 5 )   e202213682   2022.12

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/anie.202213682

    researchmap

    Other Link: https://onlinelibrary.wiley.com/doi/full-xml/10.1002/anie.202213682

  • Total Synthesis and Structure Assignment of Saptomycin H Reviewed

    Jun Shimura, Yoshio Ando, Ken Ohmori, Keisuke Suzuki

    Organic Letters   24   1439 - 1443   2022.2

     More details

    Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society ({ACS})  

    DOI: 10.1021/acs.orglett.1c04306

    researchmap

  • Model Study toward Total Synthesis of Dimeric Pyranonaphthoquinones: Synthesis of Hemi-Actinorhodin Reviewed

    Yoshio Ando, Takumi Fukazawa, Ken Ohmori, Keisuke Suzuki

    Bulletin of the Chemical Society of Japan   94 ( 4 )   1364 - 1376   2021.4

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:The Chemical Society of Japan  

    DOI: 10.1246/bcsj.20210053

    researchmap

  • Photoredox Reaction of Naphthoquinone C‐Glycoside Revisited: Insight into Stereochemical Aspect Reviewed

    Yoshio Ando, Takashi Matsumoto, Keisuke Suzuki

    Helvetica Chimica Acta   104   e2100008   2021.3

     More details

    Authorship:Lead author, Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/hlca.202100008

    researchmap

  • Thiolate-mediated Reductive Cyclizations: Scope, Limitation and Novel Mechanistic Insights Reviewed

    Yoshio Ando, Takumi Fukazawa, Ken Ohmori, Keisuke Suzuki

    Chemistry Letters   49 ( 9 )   1103 - 1106   2020.9

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:The Chemical Society of Japan  

    DOI: 10.1246/cl.200411

    researchmap

  • Total Syntheses of Structurally Complex Natural Products: Potential Reactivity of Organic Molecules Reviewed

    Yoshio Ando

    Journal of Synthetic Organic Chemistry, Japan   78 ( 4 )   304 - 316   2020.4

     More details

    Authorship:Lead author, Corresponding author  

    researchmap

  • Toward Pluramycins with Epoxy Side Chain: Syntheses of Kidamycinone and Epoxykidamycinone (Saptomycinone H) Reviewed

    Yoshio Ando, Yoshihiko Maezawa, Jun Shimura, Kei Kitamura, Takashi Matsumoto, Keisuke Suzuki

    Chemistry – An Asian Journal   15   828 - 832   2020.3

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/asia.201901807

    researchmap

  • Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-exo/6-endo Issue toward Synthesis of Pluramycin-Class Antibiotics Reviewed

    Jun Shimura, Yoshio Ando, Keisuke Suzuki

    Organic Letters   22 ( 1 )   175 - 179   2020.1

     More details

    Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society ({ACS})  

    DOI: 10.1021/acs.orglett.9b04127

    researchmap

  • α-L-Vancosamine Aryl C-Glycosides, Less Stable Anomers: A Problem in Synthesis of Pluramycin-Class Antibiotics Invited Reviewed

    Yoshio Ando

    HETEROCYCLES   101 ( 2 )   645 - 663   2020

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3987/com-19-s(f)55

    researchmap

  • Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin A Reviewed

    Yoshio Ando, Daisuke Tanaka, Ryota Sasaki, Ken Ohmori, Keisuke Suzuki

    Angewandte Chemie International Edition   58 ( 36 )   12507 - 12513   2019.9

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/anie.201906762

    researchmap

  • Thiolate-mediated reductive cyclization: asymmetric total synthesis of (+)-engelharquinone Reviewed

    Yoshio Ando, Takumi Fukazawa, Subaru Hori, Ken Ohmori, Keisuke Suzuki

    Phosphorus, Sulfur and Silicon and the Related Elements   194 ( 7 )   723 - 725   2019.7

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (international conference proceedings)  

    DOI: 10.1080/10426507.2019.1603718

    Web of Science

    Scopus

    researchmap

  • Total Synthesis of Actinorhodin Reviewed

    Mamiko Ninomiya, Yoshio Ando, Fumitaka Kudo, Ken Ohmori, Keisuke Suzuki

    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION   58 ( 13 )   4264 - 4270   2019.3

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.201814172

    Web of Science

    researchmap

  • Photoredox Reactions of Quinones Reviewed

    Yoshio Ando, Keisuke Suzuki

    Chemistry – A European Journal   24 ( 60 )   15955 - 15964   2018.10

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/chem.201801064

    researchmap

  • Intramolecular photoredox reactions of 1,2-naphthoquinone derivatives Reviewed

    Yoshio Ando, Fumihiro Wakita, Ken Ohmori, Keisuke Suzuki

    Bioorganic & Medicinal Chemistry Letters   28 ( 16 )   2663 - 2666   2018.9

     More details

    Authorship:Lead author, Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Elsevier {BV}  

    DOI: 10.1016/j.bmcl.2018.05.056

    researchmap

  • Model Reactions for the Enantioselective Synthesis of γ-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal Reviewed

    Fumihiro Wakita, Yoshio Ando, Ken Ohmori, Keisuke Suzuki

    Organic Letters   20 ( 13 )   3928 - 3932   2018.7

     More details

    Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society ({ACS})  

    DOI: 10.1021/acs.orglett.8b01475

    researchmap

  • Total Synthesis of Aryl C‐Glycoside Natural Products: Strategies and Tactics Reviewed

    Kei Kitamura, Yoshio Ando, TAKASHI MATSUMOTO, KEISUKE SUZUKI

    Chemical Reviews   Vol. 118   1495 - 1598   2017.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.chemrev.7b00380

    researchmap

  • Stereospecificity in Intramolecular Photoredox ReactiStereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (–)-Spiroxin C Reviewed

    Yoshio Ando, Atsuko Hanaki, Ryota Sasaki, Ken OHMORI, KEISUKE SUZUKI

    Angewande Chemie Inernational Edition   Vol. 56   11460 - 11465   2017.8

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.201705562

    researchmap

  • Intramolecular Photoredox Reaction of Naphthoquinone Derivatives Reviewed

    Yoshio Ando, Takashi Matsumoto, Keisuke Suzuki

    SYNLETT   28 ( 9 )   1040 - 1045   2017.6

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1055/s-0036-1589001

    Web of Science

    researchmap

  • Enantioselective Access to Bicyclo[3.2.1]octadienone Skeleton: Total Syntheses of (+)-Engelharquinone and Its Epoxide Reviewed

    Takumi Fukazawa, Yoshio Ando, Ken OHMORI, KEISUKE SUZUKI

    Organic Letters   Vol. 19   1470 - 1473   2017.3

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.orglett.7b00464

    researchmap

  • Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle Reviewed

    Juri Sakata, Yoshio Ando, Ken Ohmori, Keisuke Suzuki

    Organic Letters   17 (15) ( 15 )   3746 - 3749   2015.7

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.orglett.5b01732

    Web of Science

    researchmap

  • Toward Naphthocyclinones: Doubly Connected Octaketide Dimers with a Bicyclo[3.2.1]octadienone Core by Thiolate-Mediated Cyclization Reviewed

    Yoshio Ando, Subaru Hori, Takumi Fukazawa, Ken Ohmori, Keisuke Suzuki

    Angewandte Chemie International Edition   Vol. 54 ( 33 )   2015.6

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.201503442

    researchmap

  • Ambipolar transistor properties of 2,2′-binaphthosemiquinones Reviewed

    Toshiki Higashino, Shohei Kumeta, Sumika Tamura, Yoshio Ando, Ken Ohmori, Keisuke Suzuki, Takehiko Mori

    Journal of Materials Chemistry C   3 ( 7 )   1588 - 1594   2015.2

     More details

    Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/c4tc02467b

    Scopus

    researchmap

  • Toward the Pluramycins: Route Exploration from Dihydroxyanthrone Tricyclic Platform to an Aglycon, Saptomycinone B Reviewed

    Keisuke Suzuki, Takashi Matsumoto, Kei Kitamura, Yoshio Ando, Yoshihiko Maezawa

    HETEROCYCLES   90 ( 2 )   1240 - 1240   2015

     More details

    Publishing type:Research paper (scientific journal)   Publisher:Japan Institute of Heterocyclic Chemistry  

    DOI: 10.3987/com-14-s(k)106

    researchmap

  • Synthesis of the pluramycins 1: Two designed anthrones as enabling platforms for flexible Bis-C-glycosylation Reviewed

    Kei Kitamura, Yoshio Ando, Takashi Matsumoto, Keisuke Suzuki

    Angewandte Chemie - International Edition   53 ( 5 )   1258 - 1261   2014.1

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.201308016

    Scopus

    PubMed

    researchmap

  • Synthesis of the pluramycins 2: Total synthesis and structure assignment of saptomycin B Reviewed

    Kei Kitamura, Yoshihiko Maezawa, Yoshio Ando, Takenori Kusumi, Takashi Matsumoto, Keisuke Suzuki

    Angewandte Chemie - International Edition   53 ( 5 )   1262 - 1265   2014.1

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.201308017

    Scopus

    PubMed

    researchmap

  • Novel One-Pot Synthesis of Xanthones via Sequential Fluoride Ion-Promoted Fries-Type Rearrangement and Nucleophilic Aromatic Substitution Reviewed

    Yuuki Fujimoto, Ryohei Itakura, Hiroki Hoshi, Hikaru Yanai, Yoshio Ando, Keisuke Suzuki, Takashi Matsumoto

    SYNLETT   24 ( 19 )   2575 - 2580   2013.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1055/s-0033-1339881

    Web of Science

    researchmap

  • Preparation of L-vancosamine-related glycosyl donors Reviewed

    Kei Kitamura, Masayuki Shigeta, Yoshihiko Maezawa, Yukie Watanabe, Day-Shin Hsu, Yoshio Ando, Takashi Matsumoto, Keisuke Suzuki

    JOURNAL OF ANTIBIOTICS   66 ( 3 )   131 - 139   2013.3

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1038/ja.2013.2

    Web of Science

    researchmap

  • 34 Synthetic Study on Pluramycin-class Antibiotics(Oral Presentation)

    Kitamura Kei, Maezawa Yoshihiko, Ando Yoshio, Matsumoto Takashi, Suzuki Keisuke

    Symposium on the Chemistry of Natural Products, symposium papers   ( 54 )   199 - 204   2012.9

     More details

    Language:Japanese   Publisher:Symposium on the chemistry of natural products  

    The pluramycins constitute a class of antitumor antibiotics with an anthrapyrone chromophore with two amino sugars attached through the C-glycoside linkages. These compounds exhibit antitumor activity by specific DNA alkylation with high sequence recognition. Considerable attention has been centered at the synthesis of these compounds, where two basic problems must be addressed, (1) bis-C-glycosylation and (2) the selective construction of anthra[1,2-b]pyrone chromophore. This presentation will deal with the total synthesis of the saptomycin B. Sc(OTf)_3-promoted C-glycosylation of tricyclic bisphenol 15 with vancosaminyl acetate 2 proceeded in a regioselective manner at C7 in high yield. Further reaction with angolosaminyl acetate 4 under the similar conditions proceeded at C5 to give bis-C-glycoside 13 possessing the two amino sugar moieties at the requisite positions. This bis-C-glycoside was derived to ynone 12 via the aldol addition to chiral, optically active ynal 14. Treatment of 12 with K_2CO_3 in Me0H cleanly promoted the pyranone formation, and the following three-step oxidation gave anthraquinone 32. We are now examining the final deprotection toward the total synthesis of saptomycin B.

    DOI: 10.24496/tennenyuki.54.0_199

    CiNii Books

    researchmap

  • Design, Synthesis, and Validation of a beta-Turn Mimetic Library Targeting Protein-Protein and Peptide-Receptor Interactions Reviewed

    Landon R. Whitby, Yoshio Ando, Vincent Setola, Peter K. Vog, Bryan L. Roth, Dale L. Boger

    Journal of the American Chemical Society   volume 133   10184 - 10194   2011.5

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/ja201878v

    researchmap

  • Photochemical Reactions in Natural Product Synthesis

    ANDO Yoshio

    J. Synth. Org. Chem. Jpn.   68 ( 10 )   1067 - 1068   2010.10

     More details

    Language:Japanese   Publisher:The Society of Synthetic Organic Chemistry, Japan  

    Photochemical reactions provide powerful methods for synthesizing complex molecules. They have attracted considerable attention due to their unique reaction pathways through the excited states. This mini-review surveys some recent literatures, which show the potential and capacity of photochemical reactions in natural product total syntheses.

    DOI: 10.5059/yukigoseikyokaishi.68.1067

    CiNii Books

    researchmap

  • Efficient bis-C-aminoglycosylation toward the synthesis of the pluramycins Reviewed

    Masayuki Shigeta, Tomohiko Hakamata, Yukie Watanabe, Kei Kitamura, Yoshio Ando, Keisuke Suzuki, Takashi Matsumoto

    Synlett   ( 17 )   2654 - 2658   2010

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1055/s-0030-1258766

    Scopus

    researchmap

  • The synthesis of D-trihydroxyllysine-based oligopeptides as a hydrophilic scaffold and its application to the synthesis of bifunctional chelating agents for use as bone tracers Reviewed

    Hiroshi Tanaka, Yoshio Ando, Tsutomu Abe, Takashi Takahashi

    Chemistry - An Asian Journal   3 ( 12 )   2033 - 2045   2008.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/asia.200800250

    Scopus

    PubMed

    researchmap

  • 糖骨格を利用した分子イメージングプローブの開発研究 Reviewed

    安藤吉勇

    2007.3

     More details

    Language:Japanese   Publishing type:Doctoral thesis  

    researchmap

  • Solid-phase synthesis of epigallocatechin gallate derivatives Reviewed

    Hiroshi Tanaka, Haruko Miyoshi, Yu-Cheng Chuang, Yoshio Ando, Takashi Takahashi

    Angewandte Chemie - International Edition   46 ( 31 )   5934 - 5937   2007

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/anie.200701276

    Scopus

    PubMed

    researchmap

  • Synthesis of DTPA-conjugated (1,4)-linked 2-aminoglycosides varying in the anomeric configuration and their MRI contrast effect Reviewed

    Hiroshi Tanaka, Yoshio Ando, Masatoshi Wada, Takashi Takahashi

    Organic and Biomolecular Chemistry   3 ( 18 )   3311 - 3328   2005.9

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/b507824e

    Scopus

    researchmap

▼display all

Books

  • 月刊ファインケミカル

    安藤 吉勇( Role: Contributorキノン類への光照射を契機とするC–H結合官能基化法の開発と天然物合成への展開)

    2021 

     More details

  • Chemistry & Chemical Industry

    Yoshio Ando( Role: Contributor)

    The Chemical Society of Japan  2019.7 

     More details

  • Cutting-Edge Organic Synthesis and Chemical Biology of Bioactive Molecules

    Yoshio Ando, Kei Kitamura, Takashi Matsumoto, Keisuke Suzuki( Role: ContributorSynthetic Approaches on the Pluramycin-Class Antibiotics)

    2019 

     More details

  • 化学

    安藤 吉勇( Role: Contributor自然に倣う合成戦略:黄色色素サンタリンYの全合成)

    2016 

     More details

  • 有機合成化学協会誌

    安藤 吉勇( Role: Contributor光化学反応を利用した天然物合成 (Review de Debut))

    2010 

     More details

  • 化学

    安藤 吉勇, 高橋 孝志( Role: Contributor生体イメージング分子としてのMRI造影剤)

    2006 

     More details

▼display all

Awards

  • Seiichi Tejima Paper Award

    2021.4   Tokyo Institute of Technology   Total Synthesis of Actinorhodin

    Mamiko Ninomiya, Yoshio Ando, Fumitaka Kudo, Ken Ohmori, Keisuke Suzuki

     More details

  • Thieme Chemistry Journals Award

    2020.1   Thieme Chemistry  

    Yoshio Ando

     More details

  • Chemist Award BCA 2019

    2019.12  

    Yoshio Ando

     More details

  • Tokyo Tech Challenging Research Award

    2019.9   Tokyo Institute of Technology  

    Yoshio Ando

     More details

  • 若い世代の特別講演会

    2019.3   The Chemical Society of Japan  

    Yoshio Ando

     More details

  • Fujino–Nakamura Young Researcher Award

    2019.2   Tokyo Institute of Technology  

    Yoshio Ando

     More details

  • Incentive Award in Synthetic Organic Chemistry, Japan

    2018.2   The Society of Synthetic Organic Chemistry, Japan  

    Yoshio Ando

     More details

  • Incentive Award in School of Science, Tokyo Institute of Technology

    2017.12  

    Yoshio Ando

     More details

  • Asian Core Program/Advanced Research Network Lectureship Award (China)

    2015.11   ICCEOCA-10 / ARNCEOCA-1   Total Synthesis of (–)-Spiroxin C

    Yoshio Ando

     More details

  • Mitsui Chemicals Award in Synthetic Organic Chemistry (Japan)

    2013.2   The Society of Synthetic Organic Chemistry, Japan  

    Yoshio Ando

     More details

▼display all

Research Projects

  • キメラ準粒子の分子科学

    Grant number:24H02234  2024.4 - 2029.3

    日本学術振興会  科学研究費助成事業  学術変革領域研究(A)

    谷口 耕治, 中村 優男, 三輪 真嗣, 廣部 大地, 安藤 吉勇

      More details

    Authorship:Coinvestigator(s) 

    Grant amount:\260910000 ( Direct Cost: \200700000 、 Indirect Cost:\60210000 )

    researchmap