J. Matsumoto

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The Dimeric Form of 1,3‐Diaminoisoquinoline Derivative Rescued the Mis‐splicing of Atp2a1 and Clcn1 Genes in Myotonic Dystrophy Type 1 Mouse Model

C. Dohno, K. Nakatani, M. Nakamori, 2020, Chemistry.

Medicinal chemistry of 1-benzazepines.

K. Hino, J. Matsumoto, 1990, Progress in medicinal chemistry.

{μ-Bis(1-methylimidazol-2-yl)methane-κ2 N 3:N 3′}bis{[(1-methylimidazol-2-yl)methane-κ2 N 3,N 3′]copper(I)} bis(trifluoromethanesulfonate)

Jun Matsumoto, Yuji Kajita, Hideki Masuda, 2009, Acta crystallographica. Section E, Structure reports online.

Novel benzamides as selective and potent gastrokinetic agents. 2. Synthesis and structure-activity relationships of 4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2- morpholinyl]methyl] benzamide citrate (AS-4370) and related compounds.

S. Kato, T. Karasawa, J. Matsumoto, 1991, Journal of medicinal chemistry.

An efficient one-pot protocol for asymmetric bifunctionalization of 5,15-disubstituted porphyrins: direct access to meso activated alkenyl-substituted meso-formylporphyrins

S. Hayashi, T. Takanami, J. Matsumoto, 2011 .

Synthesis and characterization of cobalt(II) complexes with tripodal polypyridine ligand bearing pivalamide groups. Selective formation of six- and seven-coordinate cobalt(II) complexes.

Tatsuya Suzuki, H. Masuda, J. Matsumoto, 2012, Dalton transactions.

1,4-Dihydro-4-oxopyridinecarboxylic acids as antibacterial agents. 2. Synthesis and structure-activity relationships of 1,6,7-trisubstituted 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids, including enoxacin, a new antibacterial agent

J. Matsumoto, A. Minamida, H. Egawa, 1984 .

Synthesis and Reactivity of µ-η2:η2-Disulfido Dicopper(II) Complex with N,N ',N''-Trimethyl-1,3,5-cis,cis-triaminocyclohexane

H. Masuda, J. Matsumoto, Yuji Kajita, 2011 .

A facile one-pot preparation of meso-hydroxymethylporphyrins via a sequential SNAr reaction with (2-pyridyldimethylsilyl)methyllithium followed by hydrolysis and aerobic oxidation

T. Takanami, J. Matsumoto, K. Suda, 2009 .

Pyridonecarboxylic acids as antibacterial agents. 9. Synthesis and antibacterial activity of 1-substituted 6-fluoro-1,4-dihydro-4-oxo-7-(4-pyridyl)-1,8-naphthyridine-3- carboxylic acids.

J. Matsumoto, Y. Nishimura, 1987, Journal of Medicinal Chemistry.

Medium-sized cyclophanes. 15. Bromination and Lewis acid catalyzed isomerization of 8,16-diethyl[2.2]metacyclophane

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Studies on nitrofuran derivatives. 3. Novel self-condensations of 5-nitro-2-furaldehyde and 5-nitro-2-thenaldehyde.

J. Matsumoto, A. Fujita, S. Minami, 1965, Chemical & pharmaceutical bulletin.

Pyridonecarboxylic acids as antibacterial agents. VIII. An alternative synthesis of enoxacin via fluoronicotinic acid derivatives.

J. Matsumoto, H. Egawa, T. Miyamoto, 1987, Chemical & pharmaceutical bulletin.

A new synthesis of 7H-pyrido[1,2,3-de][1,4]benzoxazine derivatives including an antibacterial agent, ofloxacin.

J. Matsumoto, H. Egawa, T. Miyamoto, 1986, Chemical & pharmaceutical bulletin.

Synthesis of fluorinated pyridines by the Balz-Schiemann reaction. An alternative route to enoxacin, a new antibacterial pyridonecarboxylic acid

J. Matsumoto, A. Minamida, H. Egawa, 1984 .

A New Cinnoline Ring Construction by the Reaction of 2-Diazo-3-(2-fluorophenyl)-3-oxopropionates with Tri-n-buthylphosphine

J. Matsumoto, T. Miyamoto, 1988 .

Pyrroloquinolones and pyrazoloquinolones as potential antibacterial agents. Synthesis and antibacterial activity

J. Matsumoto, M. Fujita, H. Egawa, 1996 .

Pyridonecarboxylic Acids as Antibacterial Agents. Part 10. Synthesis and Reactions of 7-Substituted 1-Cyclopropyl-6-fluoro-1,4-dihydro-4- oxo-1,8-naphthyridine-3-carboxylic Acids as an Antibacterial Agent.

J. Matsumoto, H. Egawa, T. Miyamoto, 1988 .

Pyridonecarboxylic acids as antibacterial agents. 4. Synthesis and antibacterial activity of 7-(3-amino-1-pyrrolidinyl)-1-ethyl-6-fluoro-1,4 -dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid and its analogues.

J. Matsumoto, A. Minamida, H. Egawa, 1984, Journal of medicinal chemistry.

Pyridonecarboxylic Acids as Antibacterial Agents. Part 9. Synthesis and Antibacterial Activity of 1-Substituted 6-Fluoro-1,4-dihydro-4-oxo-7- (4-pyridyl)-1,8-naphthyridine-3-carboxylic Acids.

J. Matsumoto, Y. Nishimura, 1988 .

Highly enantioselective monoalkylation of p-chlorobenzaldehyde imine of glycine tert-butyl ester under mild phase-transfer conditions

T. Kano, K. Maruoka, T. Ooi, 2006 .

Synthesis and structure-activity relationships of 5-substituted 6,8-difluoroquinolones, including sparfloxacin, a new quinolone antibacterial agent with improved potency.

J. Matsumoto, A. Minamida, M. Fujita, 1990, Journal of medicinal chemistry.

Novel, highly potent aldose reductase inhibitors: (R)-(-)-2-(4-bromo-2-fluorobenzyl)-1,2,3,4- tetrahydropyrrolo[1,2-a]pyrazine -4-spiro-3'-pyrrolidine-1,2',3,5'-tetrone (AS-3201) and its congeners.

M. Murata, B. Fujitani, J. Matsumoto, 1998, Journal of medicinal chemistry.

Syntheses, Characterization, and Reactivities of (μ-η2:η2-Disulfido)dicopper(II) Complexes with N-Alkylated cis,cis-1,3,5-Triaminocyclohexane Derivatives

S. Hirota, H. Masuda, T. Ozawa, 2008 .

Pyrido(2,3-d)pyrimidine antibacterial agents. 3. 8-Alkyl- and 8-vinyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)pyrido(2,3-d)pyrimidine-6-carboxylic acids and their derivatives.

J. Matsumoto, S. Minami, 1975, Journal of medicinal chemistry.

Synthesis and Characterization of a (μ‐η2:η2‐Peroxido)dicopper(II) Complex with N,N′,N″‐Triisopropyl‐cis,cis‐1,3,5‐triaminocyclohexane (R3TACH, R = iPr): Selective Preparation of (μ‐η2:η2‐Peroxido)dicopper(II) and Bis(μ‐oxido)dicopper(III) Species Regulated by Substituent Groups

H. Masuda, J. Matsumoto, Yuji Kajita, 2012 .

Synthesis and antiulcer activity of the metabolites of 2-(4-ethyl-1-piperazinyl)-4-phenylquinoline dimaleate (AS-2646), a novel gastric antisecretory and antiulcer agent.

K. Hino, J. Matsumoto, K. Kawashima, 1989, Chemical & pharmaceutical bulletin.

5-Alkoxyimidazoquinolones as potential antibacterial agents. Synthesis and structure-activity relationships.

J. Matsumoto, M. Fujita, H. Egawa, 1996, Chemical & pharmaceutical bulletin.

Imidazo- and triazoloquinolones as antibacterial agents. Synthesis and structure-activity relationships.

J. Matsumoto, M. Fujita, H. Egawa, 1995, Chemical & pharmaceutical bulletin.

Pyridonecarboxylic acids as antibacterial agents. XII. Synthesis and antibacterial activity of enoxacin analogues with a variant at position 1.

J. Matsumoto, A. Minamida, Y. Nishimura, 1988, Chemical & pharmaceutical bulletin.

Syntheses of Pyrimido [4, 5-c] pyridazine Derivatives. II. A Novel Reaction of α-Diazo-β-oxo-5-(4-chloropyrimidine) propionate with Triphenyl Phosphine leading to 1, 4-Dihydro-4-oxopyrimido-[4, 5-c] pyridazine-3-carboxylate

J. Matsumoto, T. Miyamoto, S. Minami, 1978 .

PYRIDO(2,3‐D)PYRIMIDINE ANTIBACTERIAL AGENTS PART 3, 8‐ALKYL‐ AND 8‐VINYL‐5,8‐DIHYDRO‐5‐OXO‐2‐(1‐PIPERAZINYL)PYRIDO(2,3‐D)PYRIMIDINE‐6‐CARBOXYLIC ACIDS AND THEIR DERIVATIVES

J. Matsumoto, S. Minami, 1975 .

A novel class of antiulcer agents. 4-Phenyl-2-(1-piperazinyl)quinolines.

K. Hino, J. Matsumoto, K. Kawashima, 1989, Chemical & pharmaceutical bulletin.

One-step furan ring formation: Synthesis of furo[3,2-h]quinolones†

J. Matsumoto, M. Fujita, H. Egawa, 1997 .

An intramolecular cyclization of 7‐substituted 6‐fluoro‐ 1,8‐naphthyridine and ‐quinoline derivatives

J. Matsumoto, A. Minamida, Y. Nishimura, 1988 .

A new synthetic route to 7‐halo‐1‐cyclopropyl‐6‐fluoro‐1,4‐dihydro‐4‐oxoquinoline‐3‐carboxylic acid, an intermediate for the synthesis of quinolone antibacterial agents

J. Matsumoto, H. Egawa, M. Kataoka, 1987 .

Fluorinated pyrido[2,3-c]pyridazines. II. Synthesis and antibacterial activity of 1,7-disubstituted 6-fluoro-4(1H)-oxopyrido[2,3-c]pyridazine-3- carboxylic acids.

J. Matsumoto, T. Miyamoto, 1990, Chemical & pharmaceutical bulletin.

Pyridonecarboxylic Acids as Antibacterial Agents. Part 14. Synthesis and Structure-Activity Relationships of 5-Substituted 6,8-Difluoroquinolones, Including Sparfloxacin, a New Quinolone Antibacterial Agent with Improved Potency.

J. Matsumoto, A. Minamida, M. Fujita, 1990 .

A concise synthesis of (2S, 3S)-BocAHPBA and (R)-BocDMTA, chiral building blocks for peptide-mimetic HIV protease inhibitors

J. Matsumoto, M. Ikunaka, Y. Nishimoto, 2002 .

A NEW BASE‐INDUCED RING TRANSFORMATION OF PYRIDO(2,3‐D)PYRIMIDINES

J. Matsumoto, S. Minami, S. Mishio, 1979 .

Synthesis, characterization, and reactivity of a novel μ-η2:η2-diselenidodicopper(II) complex.

H. Masuda, J. Matsumoto, Yuji Kajita, 2012, Inorganic chemistry.

1,3-Dipolar cycloaddition of 5-nitro-2-furonitrile oxide.

J. Matsumoto, S. Minami, 1967, Chemical & pharmaceutical bulletin.

Pyridone-carboxylic acids as antibacterial agents. I. Synthesis and antibacterial activity of 1-alkyl-1,4-dihydro-4-oxo-1,8- and 1,6-naphthyridine-3-carboxylic acids.

J. Matsumoto, T. Hirose, S. Minami, 1982, Chemical & pharmaceutical bulletin.

An Expeditious Scalable Synthesis of (S)-2-Amino-5-methoxytetralin via Resolution

J. Matsumoto, M. Ikunaka, Y. Hirayama, 2005 .

Medium‐sized cyclophanes, 37. [n.2]metacyclophanediquinones: Synthesis, conformational studies and reduction to tetrahydroxy[n.2]metacyclophanes

T. Moriguchi, J. Matsumoto, T. Yamato, 1995 .

Medium-sized cyclophanes. Part 36. Synthesis and conformational studies of dimethoxy[m.n]metacyclophanes

J. Matsumoto, T. Yamato, M. Tashiro, 1995 .

Medium-sized cyclophanes. 19. Preparation and conformational studies of [m.n]metacyclophanes

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Medium‐Sized Cyclophanes, 20. Synthesis and Conformational Studies of syn‐ and anti‐Dihydroxy[n.2]metacyclophanes

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Synthesis and characterization of tricarbonyl–molybdenum complexes bearing monoaza-trithia-macrocyclic ligands

H. Masuda, J. Matsumoto, T. Ogawa, 2013 .

Pyrido [2, 3- d ] pyrimidine Antibacterial Agents. II. Piromidic Acid and Related Compounds

J. Matsumoto, T. Shono, S. Minami, 1971 .

Pyridonecarboxylic acids as antibacterial agents. 2. Synthesis and structure-activity relationships of 1,6,7-trisubstituted 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids, including enoxacin, a new antibacterial agent.

J. Matsumoto, A. Minamida, H. Egawa, 1984, Journal of medicinal chemistry.

An efficient one-pot procedure for asymmetric bifunctionalization of 5,15-disubstituted porphyrins: a simple preparation of meso acyl-, alkoxycarbonyl-, and carbamoyl-substituted meso-formylporphyrins.

T. Takanami, J. Matsumoto, K. Suda, 2009, Chemical communications.

[Studies on nitrofuran derivatives. IX. Reactions of 5-nitro-2-furoyl isothiocyanate and 5-nitro-2-thiofuroyl isocyanate with beta-aminocrotonates (author's transl)].

J. Matsumoto, S. Minami, S. Mishio, 1975, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Ring expansion of nitrogen-containing chloromethylheteroalicycles via aziridinium intermediates

I. Fujiwara, S. Kato, J. Matsumoto, 1994 .

Medium‐Sized Cyclophanes. Part 15. Bromination and Lewis Acid‐ Catalyzed Isomerization of 8,16‐Diethyl(2.2)metacyclophane.

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Medium-sized cyclophanes. Part 18. 5-tert-Butyl-8-substituted [2.2]metaparacyclophanes: preparation, X-Ray diffraction studies, and their treatment with Lewis acids in benzene

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Synthesis and biological activities of the optical isomers of (+/-)-4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2- morpholinyl]methyl]benzamide (mosapride).

S. Kato, J. Matsumoto, H. Harada, 1994, Chemical & pharmaceutical bulletin.

Synthesis and Biological Activities of the Optical Isomers of (.+‐.)‐4‐ Amino‐5‐chloro‐2‐ethoxy‐N‐((4‐(4‐fluorobenzyl)‐2‐morpholinyl)methyl) benzamide (Mosapride).

S. Kato, J. Matsumoto, H. Harada, 1994 .

Synthesis of 1H-pyrrolo[3,2-h]quinoline-8-amine derivatives that target CTG trinucleotide repeats.

C. Dohno, K. Nakatani, Jinxing Li, 2016, Bioorganic & medicinal chemistry letters.

Syntheses of Pyrimido [4,5-c] pyridazine Derivatives. I. A Novel Reaction of α-Diazo-β-oxo-5-(4-chloropyrimidine) propionate with Hydrazine leading to 1,2-Dihydro-4-hydroxypyrimido [4,5-c] pyridazine-3-carboxamide

J. Matsumoto, T. Miyamoto, S. Minami, 1976 .

1,4-DIHYDRO-4-OXOPYRIDINECARBOXYLIC ACIDS AS ANTIBACTERIAL AGENTS. 2. SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF 1,6,7-TRISUBSTITUTED 1,4-DIHYDRO-4-OXO-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACIDS, INCLUDING ENOXACIN, A NEW ANTIBACTERI

J. Matsumoto, A. Minamida, H. Egawa, 1984 .

PYRIDONE-CARBOXYLIC ACIDS AS ANTIBACTERIAL AGENTS. I. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 1-ALKYL-1,4-DIHYDRO-4-OXO-1,8- AND -1,6-NAPHTHYRIDINE-3-CARBOXYLIC ACIDS

J. Matsumoto, T. Hirose, S. Minami, 1983 .

Fluorocinnoline derivatives. II. Synthesis and antibacterial activity of fluorinated 1-alkyl-1,4-dihydro-4-oxocinnoline-3-carboxylic acids.

J. Matsumoto, T. Miyamoto, 1989, Chemical & pharmaceutical bulletin.

Medium‐Sized Cyclophanes, 25. Bromination of [2.n]Metacyclophan‐1‐enes and Isolation of Two Isomers of 1‐Bromo[2.n]metacyclophan‐1‐enes

J. Matsumoto, T. Yamato, M. Tashiro, 1993 .

Nitrosyl and carbene iron complexes bearing a κ(3)-SNS thioamide pincer type ligand.

Tatsuya Suzuki, H. Masuda, T. Ozawa, 2015, Dalton transactions.

A Dimeric 2,9-Diamino-1,10-phenanthroline Derivative Improves Alternative Splicing in Myotonic Dystrophy Type 1 Cell and Mouse Models.

C. Dohno, K. Nakatani, M. Nakamori, 2018, Chemistry.

A Ligand That Targets CUG Trinucleotide Repeats.

C. Dohno, K. Nakatani, Li-Ping Bai, 2016, Chemistry.

Synthesis and structure-activity relationships of 4-amino-5-chloro-2-ethoxybenzamides with six- and seven-membered heteroalicycles as potential gastroprokinetic agents.

I. Fujiwara, S. Kato, J. Matsumoto, 1995, Chemical & pharmaceutical bulletin.

Synthesis and Stereochemistry of 11‐Amino‐6,6a,7,8,9,10,10a,11‐ octahydrodibenzo(b,e)thiepines and ‐oxepines.

T. Tsukihara, J. Matsumoto, Y. Fukumoto, 1993 .

A novel class of enkephalinase inhibitors containing a C-terminal sulfo group.

T. Deguchi, J. Matsumoto, T. Sawayama, 1992, Journal of medicinal chemistry.

Medium-sized cyclophanes. Part 46.1 The preparation and novel [3.3]- and [1.5]-sigmatropic rearrangements of [n.2]cyclophanes having a spiro skeleton†

J. Matsumoto, T. Yamato, K. Fujita, 1998 .

The preparation and novel [3.3] sigmatropic rearrangement of cyclophanes having a spiro skeleton

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Medium-Sized Cyclophanes. Part 22. The Preparation and Novel (3.3) Sigmatropic Rearrangement of Cyclophanes Having a Spiro Skeleton.

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .

Medium‐Sized Cyclophanes. Part 46. The Preparation and Novel [3.3]‐ and [1.5]‐Sigmatropic Rearrangements of [n.2]Cyclophanes Having a Spiro Skeleton.

J. Matsumoto, T. Yamato, K. Fujita, 2010 .

Medium-sized cyclophanes. 16. Bromination of 8,16-dihydroxy[2.2]metacyclophanes

J. Matsumoto, T. Yamato, M. Tashiro, 1992 .