T. Katoh

发表

Synthesis and biological evaluation of novel FK228 analogues as potential isoform selective HDAC inhibitors.

Minoru Yoshida, T. Yamori, A. Ito, 2016, European journal of medicinal chemistry.

Total synthesis of the bicyclic depsipeptide HDAC inhibitors spiruchostatins A and B, 5''-epi-spiruchostatin B, FK228 (FR901228) and preliminary evaluation of their biological activity.

Minoru Yoshida, T. Yamori, H. Abe, 2009, Chemistry.

A new strategy toward the total synthesis of stachyflin, a potent anti-influenza A virus agent: concise route to the tetracyclic core structure.

T. Katoh, M. Nakatani, M. Inoue, 2002, Organic letters.

Glycogen accumulation in the renal tubular cells of spontaneously occurring diabetic WBN/Kob rats.

I. Narama, T. Katoh, M. Tsuchitani, 1990, Journal of comparative pathology.

Involvement of p21waf1/cip1 expression in the cytotoxicity of the potent histone deacetylase inhibitor spiruchostatin B towards susceptible NALM-6 human B cell leukemia cells.

T. Katoh, M. Ishikawa, Syu-Ichi Kanno, 2011, International journal of oncology.

Spiruchostatin A and B, novel histone deacetylase inhibitors, induce apoptosis through reactive oxygen species-mitochondria pathway in human lymphoma U937 cells.

Qing‐Li Zhao, T. Kondo, Peng Li, 2014, Chemico-biological interactions.

Synthesis of β‐Lapachone, a Potential Anticancer Agent from the Lapacho Tree

Koichi Narita, T. Katoh, T. Katoh, 2014 .

Trends in antimicrobial susceptibility of Streptococcus pneumoniae in the Tohoku district of Japan: a longitudinal analysis from 1998 to 2007.

M. Yasujima, Y. Shibata, M. Kaku, 2010, The Tohoku journal of experimental medicine.

In Vitro and in Vivo antitumor activity and the mechanism of siphonodictyal B in human colon cancer cells

C. Ishioka, Koichi Narita, T. Katoh, 2019, Cancer medicine.

Unified Synthesis of the Marine Sesquiterpene Quinones (+)‐Smenoqualone, (–)‐Ilimaquinone, (+)‐Smenospongine, and (+)‐Isospongiaquinone

Koichi Narita, T. Katoh, R. Saito, 2017 .

Total Synthesis of the Depsipeptide FR901375 and Preliminary Evaluation of Its Biological Activity

Minoru Yoshida, T. Yamori, A. Ito, 2016 .

Total Syntheses of Liphagal: A Potent and Selective Phosphoinositide 3-Kinase α (PI3Kα) Inhibitor from the Marine Sponge Aka coralliphaga

Koichi Narita, T. Katoh, 2018 .

Clinical effect of 3g/day administration of meropenem on severe pneumonia

T. Katoh, N. Miyashita, Hisataka Tanaka, 2013 .

Involvement of p 21 waf 1 / cip 1 expression in the cytotoxicity of the potent histone deacetylase inhibitor spiruchostatin B towards susceptible NALM-6 human B cell leukemia cells

T. Katoh, M. Ishikawa, Syu-Ichi Kanno, 2022 .

Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21waf1/cip1 on the SP-B resistance or susceptibility of human leukemia cells

T. Katoh, M. Ishikawa, Syu-Ichi Kanno, 2012, International journal of oncology.

Romidepsin (FK228) and its analogs directly inhibit phosphatidylinositol 3‐kinase activity and potently induce apoptosis as histone deacetylase/phosphatidylinositol 3‐kinase dual inhibitors

C. Ishioka, O. Takahashi, A. Oda, 2012, Cancer science.

Biochemical, biological and structural properties of romidepsin (FK228) and its analogs as novel HDAC/PI3K dual inhibitors

C. Ishioka, A. Oda, H. Shimodaira, 2015, Cancer science.

Predicting the structures of complexes between phosphoinositide 3-kinase (PI3K) and romidepsin-related compounds for the drug design of PI3K/histone deacetylase dual inhibitors using computational docking and the ligand-based drug design approach.

C. Ishioka, S. Fukuyoshi, O. Takahashi, 2014, Journal of molecular graphics & modelling.

Enantioselective Total Synthesis of (–)‐Siphonodictyal B and (+)‐8‐epi‐Siphonodictyal B with Phosphatidylinositol 3‐Kinase α (PI3Kα) Inhibitory Activity

C. Ishioka, T. Kikuchi, Koichi Narita, 2016 .

Biogenetically Inspired Total Synthesis of (+)‐Liphagal: A Potent and Selective Phosphoinositide 3‐Kinase α (PI3Kα) Inhibitor from the Marine Sponge Aka coralliphaga

T. Kikuchi, Koichi Narita, T. Katoh, 2014 .

Antitumor activity and pharmacologic characterization of the depsipeptide analog as a novel histone deacetylase/ phosphatidylinositol 3‐kinase dual inhibitor

C. Ishioka, Koichi Narita, T. Katoh, 2017, Cancer science.

Total synthesis of an enantiomeric pair of FR900482. 2. Syntheses of the aromatic and the optically active aliphatic segments

T. Katoh, S. Terashima, M. Hashimoto, 1997 .

A novel biogenetic type synthesis of (+)-hydantocidin

T. Katoh, S. Terashima, T. Yoshino, 1993 .

Spirocyclization of an N-acyliminium ion with substituted pyridine: stereoselective synthesis of tetracyclic spirolactams possessing the pyridone nucleus

H. Abe, T. Katoh, Kazuhiro Watanabe, 2010 .

SPIROCYCLIZATION OF SIX-MEMBERED CYCLIC N-ACYLIMINIUM IONS WITH A CONJUGATED DIENE

H. Abe, T. Katoh, Kazuhiro Watanabe, 2009 .

Enantioselective total synthesis of (-)-candelalides A, B and C: potential Kv1.3 blocking immunosuppressive agents.

H. Abe, T. Katoh, Kazuhiro Watanabe, 2009, Chemistry.

Effects of endotoxin (lipopolysaccharides) on experimental aspergillosis in leukemic mice

T. Katoh, T. Kaneko, M. Hotchi, 1987, Mycopathologia.

Enantiocontrolled synthesis of (4S,5S,6S)-6-benzyl-4,5-epoxy-6-hydroxy-2-cyclohexen-1-one, a model compound for the epoxycyclohexenone moiety of scyphostatin

T. Katoh, T. Izuhara, 2000 .

Enantioselective total synthesis of dysidavarone A, a novel sesquiterpenoid quinone from the marine sponge Dysidea avara.

Koichi Narita, T. Katoh, Yurie Fukui, 2014, Chemistry.

Enantioselective Total Synthesis of (+)‐Stachyflin: A Potential Anti‐Influenza A Virus Agent Isolated from a Microorganism

O. Takahashi, T. Kikuchi, T. Katoh, 2011 .

Total synthesis of (+)-stachyflin: a potential anti-influenza A virus agent.

H. Abe, T. Katoh, J. Sakurai, 2010, Chemical communications.

Highly efficient total synthesis of the marine natural products (+)-avarone, (+)-avarol, (-)-neoavarone, (-)-neoavarol and (+)-aureol.

H. Abe, T. Katoh, M. Ishikawa, 2008, Chemistry.

Enantioselective total synthesis of (-)-candelalide A, a novel blocker of the voltage-gated potassium channel Kv1.3 for an immunosuppressive agent.

T. Katoh, Kazuhiro Watanabe, M. Inoue, 2005, Organic letters.

Synthetic studies of kampanols, novel p21ras farnesyltransferase inhibitors: an efficient synthesis of the tetracyclic ABCD ring system of kampanols

T. Katoh, M. Nakatani, M. Inoue, 2003 .

Highly Improved Synthesis of (+)-Aureol via (-)-Neoavarone and (-)-Neoavarol, by Employing Salcomine Oxidation and Acid-Induced Rearrangement/Cyclization Strategy.

T. Katoh, M. Nakatani, M. Inoue, 2003 .

Studies toward the total synthesis of (−)-kampanol A: an efficient construction of the ABCD ring system

T. Katoh, M. Nakatani, M. Inoue, 2002 .

An efficient synthesis of (+)-aureol via boron trifluoride etherate-promoted rearrangement of (+)-arenarol

T. Katoh, M. Nakatani, M. Inoue, 2002 .

Studies toward the total synthesis of popolohuanone E: enantioselective synthesis of 8-O-methylpopolohuanone E.

O. Ohmori, T. Katoh, S. Terashima, 2001, Organic letters.

Studies toward the Total Synthesis of Popolohuanone E: Enantioselective Synthesis of 8-O-MethylpopolohuanoneE

O. Ohmori, T. Katoh, S. Terashima, 2001 .

Studies toward the synthesis of popolohuanone E: Synthesis of natural (+)-arenarol related to the proposed biogenetic precursor of popolohuanone E

T. Katoh, S. Terashima, M. Itoh, 1997 .

TOTAL SYNTHESIS OF DECAHYDROBENZO[d]XANTHENE SESQUITERPENOIDS AUREOL, STRONGYLIN A, AND STACHYFLIN : DEVELOPMENT OF A NEW STRATEGY FOR THE CONSTRUCTION OF A COMMON TETRACYCLIC CORE STRUCTURE

T. Katoh, 2013 .

Iridium-catalyzed oxidative lactonization and intramolecular Tishchenko reaction of delta-ketoaldehydes for the synthesis of isocoumarins and 3,4-dihydroisocoumarins.

T. Katoh, Kazuhiro Watanabe, Takeyuki Suzuki, 2005, Bioorganic & medicinal chemistry letters.

Tishchenko Reaction Using an Iridium-Ligand Bifunctional Catalyst

T. Katoh, Kazuhiro Watanabe, Takeyuki Suzuki, 2005 .

Iridium‐Catalyzed Oxidative Lactonization and Intramolecular Tishchenko Reaction of δ‐Ketoaldehydes for the Synthesis of Isocoumarins and 3,4‐Dihydroisocoumarins.

T. Katoh, Kazuhiro Watanabe, Takeyuki Suzuki, 2005 .

Ir-catalyzed oxidative desymmetrization of meso-diols.

T. Katoh, H. Sasai, Takeyuki Suzuki, 2009, Organic letters.

Model Studies towards the Total Synthesis of GKK1032s, Novel Antibiotic Anti-Tumor Agents: Enantioselective Synthesis of the Alkyl Aryl Ether Portion of GKK1032s

T. Katoh, Moriteru Asano, M. Inoue, 2005 .

Total Synthesis of Quinocarcin and Its Related Compounds

T. Katoh, S. Terashima, 1998 .

Synthetic studies on quinocarcin and its related compounds. 2.

Katsunori Tanaka, K. Nakatani, F. Matsuda, 1994 .

Synthetic studies on quinocarcin and its related compounds. 1. Synthesis of enantiomeric pairs of the ABE ring systems of quinocarcin

F. Matsuda, Yuko Kobayashi, T. Katoh, 1994 .

Synthesis of helical poly-.beta.-pyrroles. Multiple atropisomerism resulting in helical enantiomorphic conformations

T. Katoh, K. Folting, J. Huffman, 1990 .

Asymmetric synthesis of (1R,2S)-2-fluorocyclopropylamine, the key intermediate of the new generation of quinolonecarboxylic acid, DU-6859

K. Nakatani, Yuko Kobayashi, T. Katoh, 1992 .

Synthetic studies on the key component of the new generation of quinolonecarboxylic acid, DU-6859. 2.

K. Nakatani, Yuko Kobayashi, T. Katoh, 1994 .

A novel enantioselective synthesis of the key intermediate of (−)-huperzine a employing asymmetric palladium-catalyzed bicycloannulation

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Synthetic studies on the key component of the new generation of quinolonecarboxylic acid, DU-6859. 1. Synthesis of (1R,2S)-2-fluorocyclopropylamine by the use of optical resolution

K. Nakatani, Yuko Kobayashi, T. Katoh, 1994 .

Total synthesis of (+)-scyphostatin, a potent and specific inhibitor of neutral sphingomyelinase.

T. Katoh, M. Inoue, M. G. Murugesh, 2004, Angewandte Chemie.

Synthetic studies of huperzine A and its fluorinated analogues. 2. Synthesis and acetylcholinesterase inhibitory activity of novel fluorinated huperzine A analogues

N. Nakajima, T. Katoh, S. Terashima, 1998 .

Synthetic studies of huperzine A and its fluorinated analogues. 1. Novel asymmetric syntheses of an enantiomeric pair of huperzine A

T. Katoh, S. Terashima, T. Yoshino, 1998 .

Synthetic studies on quinocarcin and its related compounds. 3.

Yuko Kobayashi, T. Katoh, S. Terashima, 1994 .

Model Studies toward Scyphostatin: Synthesis of (S)-4-Benzyl-3-(p-toluenesulfonyl)-2-oxazolidinone and Its Effective Transformation to (S)-N-(1-Benzyl-2-hydroxyethyl)hexadecanamide

T. Katoh, M. Inoue, T. Izuhara, 2002 .

Synthetic studies of himbacine, a potent antagonist of the muscarinic M2 subtype receptor 1. Stereoselective total synthesis and antagonistic activity of enantiomeric pairs of himbacine and (2′S,6′R)-diepihimbacine, 4-epihimbacine, and novel himbacine congeners

T. Katoh, S. Terashima, A. Ishiwata, 2002 .

Total synthesis of natural (+)-FR900482. 2. Efficient syntheses of the aromatic and the optically active aliphatic fragments

T. Katoh, S. Terashima, M. Hashimoto, 1996 .

Enantioselective synthesis of 5-substituted- and 3,5-disubstituted-2-formylpyrrolidine derivatives, the key D-ring fragments of (−)-quinocarcin and (−)-10-decarboxyquinocarcin

T. Katoh, S. Terashima, Y. Nagata, 1993 .

STEREOSELECTIVE SYNTHESIS OF A 4a,9-DISUBSTITUTED OCTAHYDROACRIDINE FROM ISATIN

H. Abe, T. Katoh, Yoshimi Sato, 2009 .

Total Synthesis of Diterpenoid Pyrones, Nalanthalide, Sesquicillin, Candelalides A–C, and Subglutinols A, B

T. Katoh, 2014 .

Enantioselective Total Synthesis of (–)‐Subglutinols A and B: Potential Immunosuppressive Agents Isolated from a Microorganism

T. Kikuchi, T. Katoh, N. Matsumoto, 2011 .

Convergent and enantioselective total synthesis of (−)-nalanthalide, a potential Kv1.3 blocking immunosuppressant

T. Katoh, Kazuhiro Watanabe, M. Inoue, 2006 .

Tishchenko Reaction Using an Iridium‐Ligand Bifunctional Catalyst.

T. Katoh, Kazuhiro Watanabe, Takeyuki Suzuki, 2005 .

Iridium-catalyzed oxidative dimerization of primary alcohols to esters using 2-butanone as an oxidant

T. Katoh, Kazuhiro Watanabe, Takeyuki Suzuki, 2005 .

Formal total synthesis of ottelione using iridium-catalyzed oxidative desymmetrization

T. Katoh, H. Sasai, Takeyuki Suzuki, 2010 .

Total synthesis of natural (+)-FR900482. 1. Synthetic and end-game strategies

T. Katoh, S. Terashima, T. Yoshino, 1996 .

Iterative two-step strategy for C2–C4′ linked poly-oxazole synthesis using Suzuki–Miyaura cross-coupling reaction

H. Araki, T. Katoh, M. Inoue, 2007 .

Synthesis and structural elucidation of a new zooecdysteroid gerardiasterone

T. Katoh, T. Honda, M. Tsubuki, 1996 .

Synthetic studies toward GKK1032s, novel antibiotic antitumor agents: enantioselective synthesis of the fully elaborated tricyclic core via an intramolecular Diels-Alder cycloaddition.

H. Abe, T. Katoh, Moriteru Asano, 2006, The Journal of organic chemistry.

Synthesis of various model compounds for the central tricyclic ring system of popolophuanone E

T. Katoh, S. Terashima, Y. Ueki, 1996 .

Total Synthesis of Marine Sesquiterpene Quinones (+)‐Cyclospongiaquinone‐1 and (–)‐Dehydrocyclospongiaquinone‐1 with a Tetracyclic Benzo[a]xanthene Skeleton

Koichi Narita, T. Katoh, Y. Takeda, 2017 .

Effective chemoselective deprotection of 3,4-dimethoxybenzyl (3,4DMB) ethers in the presence of benzyl and p-methoxybenzyl (PMB) ethers by phenyliodine(III) bis(trifluoroacetate) (PIFA)

T. Katoh, Kazuhiro Watanabe, 2011 .

TOTAL SYNTHESIS OF AN ENANTIOMERIC PAIR OF FR900482. 1. SYNTHETIC AND END-GAME STRATEGIES

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Synthetic studies on Sch 202596, an antagonist of the galanin receptor subtype GalR1: an efficient synthesis of (±)-geodin, the spirocoumaranone part of Sch 202596

O. Ohmori, T. Katoh, M. Inoue, 2002 .

Total Synthesis of Bauhinoxepin J: A Biologically Active Dibenzo[b,f]oxepin Isolated from Bauhinia purpurea

Koichi Narita, T. Katoh, Yui Abe, 2011 .

An improved synthesis of plant growth regulating steroid brassinolide and its congeners

T. Katoh, T. Honda, T. Kametani, 1988 .

Stereoselective Synthesis of 26, 27-Bisnorbrassinolide

T. Katoh, T. Honda, T. Kametani, 1987 .

One-step stereochemical determination of four contiguous acyclic chiral centers on a steroidal side chain: a novel synthesis of brassinolide

T. Katoh, T. Honda, T. Kametani, 1986 .

Synthesis of the heptacyclic indole alkaloid (.+-.)-kopsine and related studies

T. Katoh, J. Huffman, P. Magnus, 1989 .

Effects of iron and desferrioxamine on Rhizopus infection

T. Katoh, M. Hotchi, F. Abe, 1990, Mycopathologia.

Experimental candidiasis associated with liver injury

T. Katoh, M. Hotchi, F. Abe, 1988, Mycopathologia.

Effects of Iron Metabolism on Tissue Reaction for Deep-seated Mycosis

T. Katoh, F. Abe, H. Inaba, 1989 .

Enantioselective total synthesis of dysidavarone A, a novel sesquiterpenoid quinone from the marine sponge Dysidea avara.

Koichi Narita, T. Katoh, Yurie Fukui, 2014, Chemistry.

Enantiocontrolled synthesis of the epoxycyclohexenone moieties of scyphostatin, a potent and specific inhibitor of neutral sphingomyelinase

T. Katoh, Kazuhiro Watanabe, M. Inoue, 2006 .

Studies toward the total synthesis of scyphostatin: first entry to the highly functionalized cyclohexenone segment.

T. Katoh, T. Izuhara, 2001, Organic letters.

A NOVEL TOTAL SYNTHESIS OF (+)-HIMBACINE, A POTENT ANTAGONIST OF THE MUSCARINIC RECEPTOR OF M2 SUBTYPE

T. Katoh, S. Terashima, A. Ishiwata, 1999 .

Synthesis and optical resolution of dl-cis-2-fluorocycloproplylamine, the key component of the new generation of quinolonecarboxylic acid, DU-6859

K. Nakatani, Yuko Kobayashi, T. Katoh, 1992 .

Total Synthesis of Antitumor Antibiotic FR900482

T. Katoh, S. Terashima, 1997 .

Studies toward the total synthesis of antibiotic roseophilin: A novel synthesis of the macrotricyclic part

T. Katoh, S. Terashima, N. Shibata, 1998 .

An expeditious synthesis of (2R,3S)-3-tert-butoxycarbonylamino-1-isobutylamino-4-phenyl-2-butanol, a key building block of HIV protease inhibitors

T. Katoh, S. Terashima, N. Shibata, 1997 .

A New Strategy Toward the Total Synthesis of Stachyflin (I), a Potent Antiinfluenza A Virus Agent: Concise Route to the Tetracyclic Core Structure (II).

T. Katoh, M. Nakatani, M. Inoue, 2003 .

Total synthesis of an enantiomeric pair of FR900482. 3. Completion of the synthesis by assembling the two segments

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Total Synthesis of Thailandepsin B, a Potent HDAC Inhibitor Isolated from a Microorganism.

Koichi Narita, T. Katoh, 2016, Chemical & pharmaceutical bulletin.

Low-dose spiruchostatin-B, a potent histone deacetylase inhibitor enhances radiation-induced apoptosis in human lymphoma U937 cells via modulation of redox signaling

Qing‐Li Zhao, T. Kondo, M. U. Rehman, 2016, Free radical research.

Total synthesis of burkholdacs A and B and 5,6,20-tri-epi-burkholdac A: HDAC inhibition and antiproliferative activity.

Minoru Yoshida, T. Yamori, A. Ito, 2014, European journal of medicinal chemistry.

Total synthesis of bicyclic depsipeptides spiruchostatins C and D and investigation of their histone deacetylase inhibitory and antiproliferative activities.

Minoru Yoshida, T. Yamori, A. Ito, 2013, European journal of medicinal chemistry.

Clinical effect of biapenem on nursing and healthcare-associated pneumonia (NHCAP).

T. Katoh, N. Miyashita, Y. Kawai, 2015, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A

N. Nakajima, T. Katoh, S. Terashima, 1996 .

Synthesis and Acetylcholinesterase Inhibitory Activity of Fluorinated Analogues of Huperzine A.

N. Nakajima, T. Katoh, S. Terashima, 1996 .

Total Synthesis of (+)‐Strongylin A, a Rearranged Sesquiterpenoid Hydroquinone from a Marine Sponge

T. Kikuchi, T. Katoh, Takaaki Kamishima, 2013 .

Synthetic studies on quinocarcin and its related compounds. 5.

K. Nakatani, T. Ashizawa, F. Matsuda, 1994 .

Directed synthesis of 2-spiroindolines from indole derivatives by formic acid-induced N-acyliminium ion-conjugated diene spirocyclization

H. Abe, T. Katoh, Toyoharu Kobayashi, 2015 .

An Enantioselective Synthesis of Natural (-)-Huperzine A via Cinchona Alkaloid Promoted Asymmetric Michael Reaction.

T. Katoh, S. Terashima, T. Yoshino, 1998 .

AN ENANTIOSELECTIVE SYNTHESIS OF NATURAL (-)-HUPERZINE A VIA CINCHONA ALKALOIDS-PROMOTED ASYMMETRIC MICHAEL REACTIONS

T. Katoh, S. Terashima, T. Yoshino, 1997 .

A novel approach to sesquiterpenoid benzoxazole synthesis from marine sponges: nakijinols A, B and E-G.

Koichi Narita, T. Katoh, Y. Takeda, 2018, Organic & biomolecular chemistry.

A novel approach to oxazole-containing diterpenoid synthesis from plant roots: salviamines E and F.

Koichi Narita, T. Katoh, N. Fujisaki, 2019, Organic & biomolecular chemistry.

A Concise Approach for Producing Optically Pure Carboxylic Acid Segments for the Synthesis of Bicyclic Depsipeptide Histone Deacetylase Inhibitors

C. Ishioka, Koichi Narita, T. Katoh, 2019, Synthesis.

Facile Total Synthesis of Thailandepsins D–F: Novel Bicyclic Depsipeptide Histone Deacetylase Inhibitors Isolated from a Microorganism

Koichi Narita, T. Katoh, N. Sayar, 2019, Synthesis.

TOTAL SYNTHESIS OF SPIRUCHOSTATIN A-A POTENT HISTONE DEACETYLASE INHIBITOR

H. Abe, Koichi Narita, T. Katoh, 2008 .

Total synthesis of spiruchostatin B, a potent histone deacetylase inhibitor, from a microorganism.

H. Abe, Koichi Narita, T. Katoh, 2008, Chemical communications.

Nouvel inhibiteur de phosphatidylinositol-3-kinase et composition pharmaceutique

C. Ishioka, T. Katoh, K. Saijo, 2012 .

Novel synthesis of (+)-hydantocidin based on the plausible biosynthetic pathway

N. Nakajima, T. Katoh, S. Terashima, 1996 .

A Novel Synthetic Approach to 2,2,2-Trifluoroethylidene Derivatives from Ketones.

N. Nakajima, T. Katoh, S. Terashima, 1997 .

Total synthesis and absolute configuration of otteliones A and B, novel and potent antitumor agents from a freshwater plant.

H. Araki, T. Katoh, M. Inoue, 2003, Organic letters.

Highly Improved Synthesis of (+)-Aureol via (-)-Neoavarone and (-)-Neoavarol, by Employing Salcomine Oxidation and Acid-Induced Rearrangement/Cyclization Strategy

T. Katoh, M. Nakatani, M. Inoue, 2003 .

Enantioselective Total Synthesis of Otteliones A and B, Novel and Powerful Antitumor Agents from the Freshwater Plant Ottelia alismoides

T. Katoh, 2013 .

Superficial eosinophilic gastritis in laboratory beagle dogs attributable probably to diet.

I. Narama, T. Katoh, M. Tsuchitani, 1990, Nihon juigaku zasshi. The Japanese journal of veterinary science.

Enantioselective total synthesis of otteliones A and B, novel and powerful antitumor agents from the freshwater plant Ottelia alismoides.

T. Katoh, 2013, Natural product communications.

Enantioselective total synthesis of (+)-ottelione A, (-)-ottelione B, (+)-3-epi-ottelione A and preliminary evaluation of their antitumor activity.

H. Araki, M. Kohno, T. Yamori, 2007, Chemistry.

Enantioselective Total Synthesis of 3‐epi‐Ottelione A.

H. Araki, T. Katoh, M. Inoue, 2004 .

Spirocyclization of an N-Acyliminium Ion with Substituted Pyridine: Stereoselective Synthesis of Tetracyclic Spirolactams Possessing the Pyridone Nucleus.

H. Abe, T. Katoh, Kazuhiro Watanabe, 2011 .

Spirocyclization of an N-acyliminium ion with substituted pyridine: synthesis of tricyclic spirolactams possessing pyridine or pyridone nucleus

H. Abe, T. Katoh, Kazuhiro Watanabe, 2007 .

Synthesis of (±)-12-Fluorohuperzine A, a Novel Acetylcholinesterase Inhibitor

T. Katoh, S. Terashima, M. Shikano, 1997 .

Studies toward the total synthesis of Sch 202596, an antagonist of the galanin receptor subtype GalR1: synthesis of geodin, the spirocoumaranone subunit of Sch 202596

O. Ohmori, T. Katoh, 2000 .