東北薬科大学 薬学部 分子薬化学教室

発表論文

Journal

2018年

Improved Admixture Vaccine of Fentanyl and Heroin Hapten Immunoconjugates: Antinociceptive Evaluation of Fentanyl-Contaminated Heroin

Candy S. Hwang, Lauren C. Smith, Yoshihiro Natori, Beverly Ellis, Bin Zhou, Kim D. Janda
ACS Omega 2018, 3, 11537-11543.

Ring-Closing Metathesis Entry to Dienamide Heterocycles

Hideaki Wakamatsu, Yoshimi Sasaki, Masatoshi Kawahata, Kentaro Yamaguchi, Yuichi Yoshimura
Synthesis 2018, 50, 3467-3486.

Glycosylation reactions mediated by hypervalent iodine: application to the synthesis of nucleosides and carbohydrates

Yuichi Yoshimura, Hideaki Wakamatsu, Yoshihiro Natori, Yukako Saito, Noriaki Minakawa
Beilstein J. Org. Chem. 2018, 14, 1595-1618.

Synthesis of 4'-Thionucleosides as Antitumor and Antiviral Agents.

Yuichi Yoshimura, Yukako Saito, Yoshihiro Natori, Hideaki Wakamatsu
Chem. Pharm. Bull., 2018, 66, 139-146.

Efficient Syntheses of Cocaine Vaccines and Their in Vivo Evaluation.

Atsushi Kimishima, Margaret E. Olson, Yoshihiro Natori, Kim D. Janda
ACS Med. Chem. Lett., 2018, 9, 411-416.

Efficacious Vaccine against Heroin Contaminated with Fentanyl.

Candy S. Hwang, Lauren C. Smith, Yoshihiro Natori, Beverly Ellis, Bin Zhou, Kim D. Janda
ACS Chem. Neurosci., 2018, 9, 1269-1275.

2017年

Development of a Glycosylation Reaction: A Key to Accessing Structurally Unique Nucleosides

Yuichi Yoshimura
Heterocycles, 2017, 94, 1625-1651.

Palladium-Catalyzed Regioselective Hydroarylation of Ynamides with Aryl Iodides: Easy Synthesis of Various Substituted Enamides Containing Stilbene Derivatives

Hideaki Wakamatsu, Rika Yanagisawa, Sho Kimura, Nao Osawa, Yoshihiro Natori, Yuichi Yoshimura
Synlett 2017, 28, 2135-2138.

Practical Synthesis of 4′‐Thioribonucleosides from L‐Arabinose via Novel Reductive Ring‐Contraction Reaction and Pummerer‐Type Thioglycosylation

Hideaki Wakamatsu, Kozue Nitta, Nozomi Shoji, Yoshihiro Natori, Yukako Saito, Yuichi Yoshimura
Curr. Protoc. Nucleic Acid Chem., 2017, 71, 1.43.1-1.43.12

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2016年

生物活性含窒素複素環化合物の立体選択的合成法の開発:天然物合成並びに有機触媒への応用研究 Development of Stereoselective Synthesis of Biologically active Nitrogen-heterocyclic compounds: Applications for Syntheses of Natural Product and Organocatalyst

名取 良浩,今堀 龍志,吉村 祐一
有機合成化学協会誌 :Journal of Synthetic Organic Chemistry, Japan., 2016, 74, 335-349.

Docking study and biological evaluation of pyrrolidine-based iminosugars as pharmacological chaperones for Gaucher disease

Atsushi Kato, Izumi Nakagome, Kasumi Sato, Arisa Yamamoto, Isao Adachi, Robert J. Nash, George W. J. Fleet, Yoshihiro Natori, Yasuka Watanabe, Tatsushi Imahori, Yuichi Yoshimura, Hiroki Takahatae, Shuichi Hirono
Org. Biomol. Chem., 2016, 14, 1039-1048.

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2015年

Catalytic asymmetric synthesis of (?)-E-δ-viniferin via an intramolecular C?H insertion of diaryldiazomethane using Rh2(S-TFPTTL)4

Yoshihiro Natori, Motoki Ito, Masahiro Anada, Hisanori Nambu, Shunichi Hashimoto
Tetrahedron Letters 2015, 56, 4324-4327.

Construction of an Isonucleoside on a 2,6-Dioxobicyclo[3.2.0]-heptane Skeleton

Yuichi Yoshimura, Satoshi Kobayashi, Hitomi Kaneko, Takeshi Suzuki, Tomozumi Imamichi
Molecules 2015, 20, 4623-4634.

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2014年

A Mouse Model of Peripheral Post-Ischemic Dysesthesia: Involvement of Reperfusion-Induced Oxidative Stress and TRPA1 Channel

Sasaki A, Mizoguchi S, Kagaya K, Shiro M, Sakai A, Andoh T, Kino Y, Taniguchi H, Saito Y, Takahata H, Kuraishi Y.
J. Pharmacol. Exp. Ther., 2014, 351, 568-575.

Synthesis and biological evaluation of α-1-C-4′-arylbutyl-L-arabinoiminofuranoses, a new class of α-glucosidase inhibitors

Yoshihiro Natori, Toshihiro Sakuma, Yuichi Yoshimura, Kyoko Kinami, Yuki Hirokami, Kasumi Sato, Isao Adachi, Atsushi Kato, Hiroki Takahata
Bioorg. Med. Chem. Lett., 2014, 24, 3298-3301.

Asymmetric synthesis of 2,5-disubstituted 3-hydroxypyrrolidines based on stereodivergent intramolecular iridium-catalyzed allylic aminations

Yoshihiro Natori, Shunsuke Kikuchi, Takahiro Kondo, Yukako Saito, Yuichi Yoshimura, Hiroki Takahata
Org. Biomol. Chem., 2014, 12, 1983-1994.

Synthesis of a Dihydropyranonucleoside Using an Oxidative Glycosylation Reaction Mediated by Hypervalent Iodine

Hiroya Kan-no, Yukako Saito, Shun Omoto, Sakie Minato, Hideaki Wakamatsu, Yoshihiro Natori, Tomozumi Imamichi, Hiroki Takahata, Yuichi Yoshimura
Synthesis 2014, 46, 879-886.

Gabapentin inhibits bortezomib-induced mechanical allodynia through supraspinal action in mice.

Kitamura R., Andoh T., Miyao S., Saito Y., Takahata H., Kuraishi Y.
J Pharmacol Sci, 2014, 124, 502-510.

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2013年

Design and Synthesis of A Nucleoside and A Phosphonate Analogue Constructed on A Branched-threo-tetrofuranose Skeleton

Y. B. Kiran, Hideaki Wakamatsu, Yoshihiro Natori, Hiroki Takahata and Yuichi Yoshimura
Tetrahedron Letters 2013, 54, 3949-3952.

A Facile Synthesis of Fully Protected meso-Diaminopimelic Acid (DAP) and Its Application to the Preparation of Lipophilic N-Acyl iE-DAP

Yukako Saito, Yuichi Yoshimura, Hideaki Wakamatsu, Hiroki Takahata
Molecules 2013, 18, 1162-1173.

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2012年

α-1-C-Butyl-1,4-dideoxy-1,4-imino-L-arabinitol as a Second-Generation Iminosugar-Based Oral α-Glucosidase Inhibitor for Improving Postprandial Hyperglycemia

Atsushi Kato, Erina Hayashi, Saori Miyauchi, Isao Adachi, Tatsushi Imahori, Yoshihiro Natori, Yuichi Yoshimura, Robert J. Nash, Hideyuki Shimaoka, Izumi Nakagome, Jun Koseki, Shuichi Hirono, Hiroki Takahata
J. Med. Chem. 2012, 55, 10347-10362.

Asymmetric Synthesis of 1-Alkyl-2-deoxyiminofuranoses via The Iridium-catalyzed Intramolecular Cyclization of an Allylic Carbonate

Yoshihiro Natori, Shunsuke Kikuchi, Yuichi Yoshimura, Atsushi Kato, Isao Adachi, Hiroki Takahata
Heterocycles, 2012, 86, 1401-1417.

Recent Advances in Cyclonucleosides: C-Cyclonucleosides and Spore Photoproducts in Damaged DNA

Yuichi Yoshimura, Hiroki Takahata
Molecules, 2012, 17, 11630-11654.

A New Route to N1-Substituted Uracil Derivatives Using Hypervalent Iodine

Yuichi Yoshimura, Hiroya Kan-no, Y. B. Kiran, Yoshihiro Natori, Yukako Saito, Hiroki Takahata
Synthesis 2012, 44, 1163-1170.

Asymmetric Synthesis of 2-Propylisofagomine Using Allylic Hydroxy Group Accelerated Ring-Closing Enyne Metathesis

Taguchi, T.; Imahori, T.; Yoshimura, Y.; Kato, A.; Adachi, I.; Kawahata, M.; Yamaguchi, K.; Takahata, H.
Heterocycles 2012, 84, 929-944.

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2011年

An Access to the β-Anomer of 4’-Thio-C-ribonucleosides: Hydroboration of 1-C-Aryl- or 1-C-Heteroaryl-4-thiofuranoid Glycals and Its Regiochemical Outcome

Haraguchi, K.; Horii, C.; Yoshimura, Y.; Ariga, F.; Tadokoro, A.; Tanaka, H.
J. Org. Chem. 2011, 76, 8658-8669.

Docking and SAR studies of D- and L-isofagomine isomers as human β-glucocerebrosidase inhibitors

Kato, A.; Miyauchi, S.; Kato, N.; Nash, R. J.; Yoshimura, Y.; Nakagome, I.; Hirono, S.; Takahata, H.; Adachi, I.
Bioorg. Med. Chem. 2011, 19, 3558-3568.

Synthesis of 5-Thiodidehydropyranylcytosine Derivatives as Potential anti-HIV Agents

Yoshimura, Y.; Yamazaki, Y.; Saito, Y.; Natori, Y.; Imamichi, T.; Takahata, H.
Bioorg. Med. Chem. Lett. 2011, 21, 3313-3316.

The synthesis and biological evaluation of 1-C-alkyl-L-arabinoiminofuranoses, a novel class of α-glucosidase inhibitors

Natori, Y.; Imahori, T.; Murakami, K.; Yoshimura, Y.; Nakagawa, S.; Kato, A.; Adachi, I.; Takahata, H.
Bioorg. Med. Chem. Lett. 2011, 21, 738-741.

Ring-opening metathesis and ring-closing metathesis of bicyclo[4.2.0]octene-ynes: Application to the synthesis of tricyclic compounds

Wakamatsu, H.; Hareyama, S.; Takeshita, M.
Arkivoc 2011, (iv), 104-114.

Catalytic enantioselective C-H functionalization of indoles with α-diazopropionates using chiral dirhodium(II) carboxylates: asymmetric synthesis of the (+)-α-methyl-3-indolylacetic acid fragment of acremoauxin A

Takayuki Goto, Yoshihiro Natori, Koji Takeda, Hisanori Nambu, Shunichi Hashimoto.
Tetrahedron: Asymmetry 2011, 22, 907-915.

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2010年

Chemoselective O-tert-butoxycarbonylation of phenols using 6,7-dimethoxyisoquinoline as a novel organocatalyst

Saito, Y.; Yoshimura, Y.; Takahata, H.
Tetrahedron Lett. 2010, 51, 6915-6917.

Synthesis and Antiviral Evaluation of α-D-2’,3’-Didehydro-2’,3’-dideoxy-3’-C-hydroxy- methyl Nucleosides

Yamada, K.; Hayakawa, H.; Sakata, S.; Ashida, N.; Yoshimura, Y.
Bioorg. Med. Chem. Lett., 2010, 20, 6013-6016.

Design and Synthesis of Isonucleosides Constructed on a 2-Oxa-6-thiabicyclo[3.2.0]heptane Scaffold

Yoshimura, Y.; Asami, K.; Imamichi, T.; Kuroda, T.; Shiraki, K.; Takahata, H.
J. Org. Chem.2010, 75, 4161-4171.

Copper-Free Sonogashira Cross-Coupling of Ynamides: Easy Access to Various Substituted Ynamides from Nonsubstituted Ynamides

Wakamatsu, H.; Takeshita, M.
Synlett 2010, 2322-2324.

Ring-closing Metathesis of Ene-ynamide: -Application to the Synthesis of Medium-sized Cyclic Dienamide-

Wakamatsu, H.; Sakagami, M.; Hanata, M.; Takeshita, M.; Mori, M.
Macromol. Symp. 2010, 293, 5-9.

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2009年

Synthesis of 1-(5,6-Dihydro-2H-thiopyran-2-yl)uracil by a Pummerer-type Thioglycosylation Reaction: The Regioselectivity of Allylic Substitution

Yoshimura, Y.; Yamazaki, Y.; Saito, Y.; Takahata, H.
Tetrahedron 2009, 65, 9091-9102.

Modified 3-Hydroxypipecolic Acid Derivatives as an Organocatalyst

Yoshimura,Y.; Ohara, C.; Miyagawa, T.; Takahata, H.
Heterocycles 2009, 77, 635-644. (Note)

Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C–H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan

Natori, Y.; Tsutsui, H.; Sato, N.; Nakamura, S.; Nambu, H.; Shiro, M.; Hashimoto, S.
J. Org. Chem., 2009, 74, 4418-4421.

Catalytic asymmetric Synthesis of both enantiomers of pyrrolizidines 223H’, 239K’, 265H’, and 267H’ found in Msdagascan frogs (Mantella) and their affinities for nicotinic acetylcoline receptor

Saito, Y.; Takahashi, S.; Azerb, N.; Eldefrawi, A. T.; Eldefrawi, M. E.; Takahata , H.
Heterocycles, 2009, 79, 1043-1060.

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2008年

Acceleration Effect of Allylic Hydroxy Group on Ring-Closing Enyne Metathesis of Terminal Alkynes: Scope, Application and Mechanistic Insights

Imahori, T.; Ojima, H.; Yoshimura, Y.; Takahata, H.
Chem. Eur. J. 2008, 14, 10762-10771.

A New Entry to Carbocyclic Nucleosides: Oxidative Coupling Reaction of Cycloalkenylsilanes with a Nucleobase Mediated by Hypervalent Iodine Reagent

Yoshimura, Y.; Ohta, M.; Imahori, T.; Imamichi, T.; Takahata, H.
Org. Lett., 2008, 10, 3449-3452.

Synthesis of Both Enantiomers of Hydroxypipecolic Acid Derivatives Equivalent to 5-Azapyranuronic Acids and Evaluation of their Inhibitory Activities against Glycosidases

Yoshimura,Y.; Ohara, C.; Imahori, T.; Saito, Y.; Kato, A.; Miyauchi, S.; Adachi, I.; Takahata, H.
Bioorg. Med. Chem., 2008, 16, 8273-8286.

Synthesis of all stereoisomers of 3-hydroxypipecolic acid and 3-hydroxy-4,5-dehydropipecolic acid and their evaluation as glycosidase inhibitors.

Ohara, C.; Takahashi, R.; Miyagawa, T.; Yoshimura,Y.; Kato, A.; Adachi, I.; Takahata, H.
Bioorg. Med. Chem. Lett., 2008, 18, 1810-1813.

Synthesis of Imidazolium-tagged Ruthenium Carbene Complex: Remarkable Activity and Reusability in Regard to Olefin Metathesis in Ionic Liquids

Wakamatsu, H.; Saito, Y.; Masubuchi, M.; Fujita, R.
Synlett 2008, 1805-1808.

Carboxamidation of carboxylic acids with 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without base

Saito, Y.; Ouchi, H.; Takahata, H.
Tetrahedron 2008, 64, 11129-11135.

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2007年

A straightforward stereoselective synthesis of meso-(S,S)-and (R,R)-2,6-diaminopimelic acids from cis-1,4-diacetoxycyclohept-2-ene

Saito, Y.; Shinkai, T.; Yoshimura, Y.; Takahata, H.
Bioorg. Med. Chem. Lett., 2007, 17, 5894-5896.

Design and Synthesis of a Novel Ring-expanded 4’-Thio-apio-nucleoside Derivatives

Yoshimura, Y.; Yamazaki, Y.; Kawahata, M.; Yamaguchi, K.; Takahata, H.
Tetrahedron Lett. 2007, 48, 4519-4522.

Asymmetric Synthesis of All Stereoisomers of Isofagomine using [2,3]-Wittig Rearrangement

Mihara, Y.; Ojima, H.; Imahori, T.; Yoshimura, Y.; Ouchi, H.; Takahata, H.
Heterocycles. 2007, 72, 633-645.

A New Preparation of Homochiral N-Protected 5-Hydroxy-3-piperidenes, Promising Chiral Building Blocks, by Palladium-Catalyzed Deracemization of Their Alkyl Carbonates

Takahata, H.; Suto, Y.; Kato, E.; Yoshimura, Y.; Ouchi, H.
Adv. Synth. Catal. 2007, 349, 685-693.

Synthesis of 6,5’-C-Cyclouridine by a Novel Tandem Radical Hydrogen Transfer and Cyclization Reaction

Yoshimura, Y.; Yamazaki, Y.; Wachi, K.; Satoh, S; Takahata, H.
Synlett 2007, 111-114.

Synthesis of Pyrrolizidine, Indolizidine, and Quinolizidine Derivatives Using Ruthenium-Catalyzed Ring-Opening Metathesis and Ring-Closing Metathesis of Cycloalkene-ynes

Wakamatsu, H.; Sato, Y.; Fujita, R.; Mori, M.
Adv. Synth. Catal. 2007, 349(7), 1231-1246.

An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation

Saito, Y.; Okamoto, N.; Takahata, H.
Beils. J. Org. Chem., 2007, 3, 37.

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2006年

New Synthesis of (±)-Isonucleosides

Yoshimura, Y.; Asami, K.; Matsui, M.; Tanaka, H.; Takahata, H.
Org. Lett. 2006, 8, 6015-6018.

A Practical Synthesis of 4'-Thioribonucleosides

Yoshimura, Y.; Kuze, T.; Ueno, M.; Komiya, F.: Haraguchi, K.; Tanaka, H.; Kano, F.; Yamada, K.; Asami, K.; Kaneko, N.; Takahata, H.
Tetrahedron Lett. 2006, 47, 591-594.

ROM-RCM of Azabicycloheptene Derivatives - Study of Products Distribution by the Substituent on Alkyne

Mori, M.; Wakamatsu, H.; Sato, Y.; Fujita, R.
J. Mol. Catal. A: Chem. 2006, 254(1-2), 64-67.

Synthesis of Cyclic Dienamide Using Ruthenium-Catalyzed Ring-Closing Metathesis of Ene-ynamide

Mori, M.; Wakamatsu, H.; Saito, N.; Sato, Y.; Narita, R.; Sato, Y.; Fujita, R.
Tetrahedron 2006, 62(16), 3872-3881.

Novel Diels-Alder reaction of 4-nitro-1(2H)-isoquinolones

Fujita, R.; Wakayanagi, S.; Wakamatsu, H.; Matsuzaki, H.
Chem. Pharm. Bull. 2006, 54, 209-212.

Synthesis of 5(6H)-phenanthridones using Diels-Alder reaction of 3-nitro-2(1H)-quinolones acting as dienophiles

Fujita, R.; Yoshisuji, T.; Wakayanagi, S.; Wakamatsu, H.; Matsuzaki, H
Chem. Pharm. Bull. 2006, 54, 204-208.

Ruthenium-Catalyzed ROM-RCM of Cyclopentene-yne. Concise Synthesis of a Pyrrolizidine Derivative

Wakamatsu, H.; Sato, Y.; Fujita, R.; Mori, M.
Heterocycles 2006, 67(1), 89-93.

A Novel tert-butoxycarbonylation reagent: 1-tert-Butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)

Saito, Y.; Ouchi, H.; Takahata, H.
Tetrahedron, 2006, 62, 11599-11607.

A novel 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI)-catalyzed esterification of N-protected amino acids with nearly equimolar amounts of alcohols in the presence of Boc2O

Saito, Y.; Watanabe, T.; Takahata, H.
Tetrahedron Lett., 2006, 47, 3099-3102.

A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2- symmetric 2,6-diallylpiperidine carboxylic acid methyl ester

Takahata, H.; Saito, Y.; Ichinose, M.
Org. Biomol. Chem., 2006, 4, 1587-1595.

Enantioselective Synthesis of 3-Arylindan-1-ones via Intramolecular C–H Insertion Reactions of α-Diazo-β-ketoesters Catalyzed by Chiral Dirhodium(II) Carboxylates

Natori, Y.; Anada, M.; Nakamura, S.; Nambu, H.; Hashimoto, S.
Heterocycle, 2006, 70, 635-646.

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2005年

Synthesis of Isoquinoline Derivatives Using ROM-RCM of Cyclobutene-yne

Mori, M.; Wakamatsu, H.; Tonogaki, K.; Fujita, R.; Kitamura, T.; Sato, Y.
J. Org. Chem. 2005, 70(3), 1066-1069.

Simple and mild esterification of N-Protected amino acids with nearly equimolar amounts of alcohols using 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline

Saito, Y.; Yamaki, T.; Kohashi, F.; Watanabe, T.; Ouchi, H.; Takahata, H.
Tetrahedron Lett., 2005, 46, 1277-1279.

Biological properties of D- and L-1-deoxyazasugars.

Atsushi Kato, Noriko Kato, Erika Kano, Isao Adachi, Kyoko Ikeda, Liang Yu, Tadashi Okamoto, Yasunori Banba, Hidekazu Ouchi, Hiroki Takahata, Naoki Asano
J. Med. Chem., 2005, 48, 2036-2044.

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2004年

Novel Stereoselective Entry to 2'-β-Carbon-Substituted 2'-Deoxy-4'-thionucleosides from 4-Thiofuranoid Glycals

Haraguchi, K.; Shiina, N.; Yoshimura, Y.; Shimada, H.; Hashimoto, K.; Tanaka, H.
Org. Lett. 2004, 6, 2645-2648.

Lithiation at the 6-Position of Uridine with Lithium Hexamethyldisilazide: Crucial Role of Temporary Silylation

Yoshimura, Y.; Kumamoto, H.; Baba, A.; Tanaka, H.
Org. Lett. 2004, 6, 1793-1795.

Inhibitory Effects of 9-(4-Thio-β-D-ribo-pentofuranosyl)guanine on Tumor Growth and Angiogenesis

Miura, S.; Yamada, K.; Kano, F.; Yoshimura, Y.
Biol. Pharm. Bull. 2004, 27, 520-523.

ROM-RCM of Cycloalkene-yne

Kitamura, T.; Kuzuba, Y.; Sato, Y.; Wakamatsu, H.; Fujita, R.; Mori, M.
Tetrahedron 2004, 60(34), 7375-7389.

An Easily Assembled Highly Active Ruthenium Initiator for Olefin Metathesis

Buschmann, N.; Wakamatsu, H.; Blechert, S.
Synlett 2004, 667-670.

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総説

Pummerer型チオグリコシル化反応の開発とヌクレオシド合成への応用

吉村 祐一
東北薬科大学研究誌、第61号、p.1-10 (2014).

グリコシド結合形成反応の開発と新規生物活性ヌクレオシド誘導体合成への展開

吉村 祐一、高畑 廣紀
有機合成化学協会詩、第67巻、p.798-808 (2009).

コンホメーション固定型アナログである炭素環シクロヌクレオシドの合成と応用研究

吉村 祐一
東北薬科大学研究誌、第55号、p.9-22 (2008).

解説

免震構造はいかに有効か── 被害が最少限にとどまった東北薬科大学

吉村 祐一
月刊化学、2011年12月号、p.17-21 (2011).

33年前の震災からの教訓を生かして-免震構造によって守られた大学

高柳 元明,吉村 祐一,安藤 隆一郎,小島 修樹
日本生理学会雑誌,第74巻,p.151-153 (2012).

著書

中分子創薬に資するペプチド・核酸・糖鎖の合成技術(分担執筆)

吉村 祐一、若松 秀章、名取 良浩、斎藤 有香子
CMC出版、2018年、2月

無機化合物・錯体 ?生物無機化学の基礎? 第2版(分担執筆)

吉村 祐一、高畑 廣紀
廣川書店、2010年、11月

無機化合物・錯体 ?生物無機化学の基礎?(分担執筆)

吉村 祐一、高畑 廣紀
廣川書店、2005年、2月

Design and New Types of Antitumor Nucleosides: The Synthesis and Antitumor Activity of 2'-Deoxy-(2'-C-substituted)cytidines

Matsuda, A.; Azuma, A.; Nakajima, Y.; Takenuki, K.; Dan, A.; Iino, T.; Yoshimura, Y.; Minakawa, N.; Tanaka, M.; Sasaki, T.
in Nucleosides Nucleotides as Antitumor and Antiviral Agents; Chu, C. K.; Baker, D. C. Eds.; Plenum Publishing Co., New York, 1993, 1-22.

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