T. Nishikawa

发表

Learning-method control applied to microcomputer-assisted pH titrations

T. Nishikawa, I. Ogasawara, Tai Harada, 1981 .

Synthetic Route to Oscillatoxin D and Its Analogues.

T. Nishikawa, Atsuo Nakazaki, Yoshihiko Nokura, 2017, Organic letters.

New synthetic route of guanidine from trichloroacetamide for tetrodotoxin and its related compounds

N. Yamamoto, M. Isobe, T. Nishikawa, 1999 .

Stereocontrolled Synthesis of (-)-5,11-Dideoxytetrodotoxin.

N. Yamamoto, M. Isobe, T. Nishikawa, 1999 .

Synthesis of Model Compound Containing an Indole Spiro-β-lactam Moiety with Vinylchloride in Chartellines

M. Isobe, T. Nishikawa, Shigeo Kajii, 2004 .

Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, an unnatural analogue of puffer fish toxin.

D. Urabe, M. Isobe, T. Nishikawa, 2002, Chemistry.

Unexpected metal-free transformation of gem-Dibromomethylenes to ketones under acetylation conditions.

K. Miyamoto, T. Nishikawa, Atsuo Nakazaki, 2015, Chemistry, an Asian journal.

Inhibition of veratridine-induced delayed inactivation of the voltage-sensitive sodium channel by synthetic analogs of crambescin B.

M. Yotsu-Yamashita, K. Konoki, M. Wakamori, 2017, Bioorganic & medicinal chemistry letters.

A concise synthesis of peramine, a metabolite of endophytic fungi

S. Ito, T. Nishikawa, Yuta Yamamoto, 2018, Bioscience, biotechnology, and biochemistry.

Hydrolysis of Sasa senanensis culm with dilute sulfuric acid for production of a fermentable substrate

M. Aoyama, T. Nishikawa, M. Miura, 2011 .

Synthesis of Oxy-Functionalized Steroidal Skeletons via Mizoroki-Heck and Intramolecular Diels-Alder Reactions.

Shogo Watanabe, T. Nishikawa, Atsuo Nakazaki, 2019, Organic letters.

Biomimetic Synthesis of the CDE Ring Moiety of Physalins, Complex 13,14-Secosteroids.

T. Nishikawa, Atsuo Nakazaki, Yusuke Araki, 2021, Organic letters.

Identification of a Fluorescent Compound in the Cuticle of the Train Millipede Parafontaria laminata armigera

T. Nishikawa, M. Kuse, N. Tani, 2010, Bioscience, biotechnology, and biochemistry.

An almost nontoxic tetrodotoxin analog, 5,6,11-trideoxytetrodotoxin, as an odorant for the grass puffer

T. Nishikawa, H. Abe, Yasuhisa Noguchi, 2021, Scientific Reports.

Synthesis of beta-analogues of C-mannosyltryptophan, a novel C-glycosylamino acid found in proteins.

M. Isobe, T. Nishikawa, Y. Koide, 2006, Organic & biomolecular chemistry.

Stereocontrolled syntheses of α-C-mannosyltryptophan and its analogues

M. Isobe, T. Nishikawa, Shigeo Kajii, 2005 .

Alpha-C-mannosyltryptophan is not recognized by conventional mannose-binding lectins.

C. Sato, K. Kitajima, M. Isobe, 2004, Bioorganic & medicinal chemistry.

A Concise Synthesis of a Highly Strained Cyclobutane in Solanoeclepin A by Radical Cyclization

T. Nishikawa, M. Adachi, T. Komada, 2012 .

New regiocontrolled syntheses of pyrrolopyrazinones and its application to the synthesis of peramine

T. Nishikawa, Atsuo Nakazaki, Yuta Yamamoto, 2017 .

Synthesis of Novel α-C-Glycosylamino Acids and Reverse Regioselectivity in Larock's Heteroannulation for the Synthesis of the Indole Nucleus

M. Isobe, T. Nishikawa, Kyoko Wada, 2002, Bioscience, biotechnology, and biochemistry.

An efficient total synthesis of optically active tetrodotoxin from levoglucosenone.

D. Urabe, M. Isobe, T. Nishikawa, 2006, Chemistry, an Asian journal.

Synthesis and antitumor activity of water-soluble enediyne compounds related to dynemicin A.

T. Jomori, M. Isobe, T. Nishikawa, 1997, Bioorganic & medicinal chemistry.

Structure-activity relationships of cyclic enediynes related to dynemicin A. I. Synthesis and antitumor activity of 9-acetoxy enediynes equipped with aryl carbamate moieties.

T. Jomori, M. Isobe, T. Nishikawa, 1997, Bioorganic & medicinal chemistry.

Synthesis of both enantiomers of dynemicin a model compound. New remote asymmetric induction in acetylide addition into quinoline nucleus as key step

M. Isobe, T. Nishikawa, Maki Yoshikai, 1994 .

Differential binding of tetrodotoxin and its derivatives to voltage‐sensitive sodium channel subtypes (Nav1.1 to Nav1.7)

M. Yotsu-Yamashita, K. Konoki, M. Wakamori, 2017, British journal of pharmacology.

De Novo Synthesis of Possible Candidates for the Inagami-Tamura Endogenous Digitalis-like Factor.

Keiko Hashimoto, T. Nishikawa, Atsuo Nakazaki, 2017, The Journal of organic chemistry.

First asymmetric total synthesis of tetrodotoxin.

M. Isobe, T. Nishikawa, Norio Ohyabu, 2003, Journal of the American Chemical Society.

Domestic cat damage to plant leaves containing iridoids enhances chemical repellency to pests

J. Hurst, T. Nishikawa, M. Miyazaki, 2022, iScience.

The characteristic response of domestic cats to plant iridoids allows them to gain chemical defense against mosquitoes

R. Beynon, T. Yamashita, J. Hurst, 2021, Science Advances.

Green spotted puffers can detect an almost nontoxic TTX analog odor using crypt olfactory sensory neurons

H. Abe, T. Nishikawa, Takehisa Suzuki, 2021, bioRxiv.

Grass puffer can smell TTX analog 1 Title : Almost nontoxic tetrodotoxin analog , 5 , 6 , 11-trideoxytetrodotoxin , 1 as an olfactory chemoattractant for the grass puffer 2 Running title : Grass puffer can smell TTX analog 3

T. Nishikawa, H. Abe, Yasuhisa Noguchi, 2021 .

Local Differences in the Toxin Amount and Composition of Tetrodotoxin and Related Compounds in Pufferfish (Chelonodon patoca) and Toxic Goby (Yongeichthys criniger) Juveniles

H. Sugita, O. Arakawa, T. Nishikawa, 2022, Toxins.

Total Syntheses and Determination of Absolute Configurations of Cep-212 and Cep-210, Predicted Biosynthetic Intermediates of Tetrodotoxin Isolated from Toxic Newt.

M. Yotsu-Yamashita, T. Nishikawa, Y. Kudo, 2019, Organic letters.

First Identification of 5,11-Dideoxytetrodotoxin in Marine Animals, and Characterization of Major Fragment Ions of Tetrodotoxin and Its Analogs by High Resolution ESI-MS/MS

V. Paul, M. Yotsu-Yamashita, K. Konoki, 2013, Marine drugs.

Studies towards the synthesis of chartelline C.

T. Nishikawa, Atsuo Nakazaki, Yoshiki Nakane, 2020, The Journal of organic chemistry.

One-pot transformation of trichloroacetamide into readily deprotectable carbamates.

D. Urabe, M. Isobe, T. Nishikawa, 2006, Organic letters.

The Synthesis of Simplified Analogues of Crambescin B Carboxylic Acid and Their Inhibitory Activity of Voltage-Gated Sodium Channels: New Aspects of Structure–Activity Relationships

M. Yotsu-Yamashita, T. Nishikawa, Atsuo Nakazaki, 2022, HETEROCYCLES.

Asymmetric synthesis of crambescin A-C carboxylic acids and their inhibitory activity on voltage-gated sodium channels.

M. Yotsu-Yamashita, T. Nishikawa, Atsuo Nakazaki, 2016, Organic and biomolecular chemistry.

Synthesis of crambescin B carboxylic acid, a potent inhibitor of voltage-gated sodium channels.

M. Yotsu-Yamashita, T. Nishikawa, Atsuo Nakazaki, 2014, Organic & biomolecular chemistry.

Palladium-Catalyzed Cascade Wacker/Allylation Sequence with Allylic Alcohols Leading to Allylated Dihydropyrones

T. Nishikawa, Atsuo Nakazaki, Wen-Yu Huang, 2017, ACS omega.

Synthetic studies on pactamycin, a potent antitumor antibiotic

M. Isobe, T. Nishikawa, Atsuo Nakazaki, 2012 .

Regioselectivity of Larock Indole Synthesis Using Functionalized Alkynes

M. Isobe, T. Nishikawa, H. Yoshimura, 2008, Bioscience, biotechnology, and biochemistry.

A Synthetic Strategy for Saxitoxin Skeleton by a Cascade Bromocyclization: Total Synthesis of (+)-Decarbamoyl-α-saxitoxinol.

T. Nishikawa, Atsuo Nakazaki, Sohei Ueno, 2016, Organic letters.

A synthetic route to the saxitoxin skeleton: synthesis of decarbamoyl α-saxitoxinol, an analogue of saxitoxin produced by the cyanobacterium Lyngbya wollei.

T. Nishikawa, Yusuke Sawayama, 2011, Angewandte Chemie.

Improved Conditions for Facile Overman Rearrangement(1).

M. Isobe, T. Nishikawa, Norio Ohyabu, 1998, The Journal of organic chemistry.

A Divergent Approach to the Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives.

T. Nishikawa, Susumu Kobayashi, Atsuo Nakazaki, 2016, Chemistry, an Asian journal.

Synthesis of a C–N Axially Chiral N-Arylisatin through Asymmetric Intramolecular N-Arylation

Keitaro Miyagawa, T. Nishikawa, Atsuo Nakazaki, 2015 .

Methodologies for synthesis of heterocyclic compounds

N. Yamamoto, M. Isobe, T. Nishikawa, 1992 .

Synthetic studies on dynemicin A. New quinoline synthesis for C, D and E rings.

M. Isobe, T. Nishikawa, 1994 .

Synthetic studies on (−)-tetrodotoxin (3) nitrogenation through overman rearrangement and guanidine ring formation

M. Isobe, T. Nishikawa, T. Goto, 1990 .

Synthetic studies on tetrodotoxin (1) stereocontrolled synthesis of the cyclohexane moiety

M. Isobe, T. Nishikawa, T. Goto, 1987 .

Synthesis of Bicyclic Hydroxy Lactone Intermediates toward (-)-Tetrodotoxin

N. Yamamoto, M. Isobe, T. Nishikawa, 1995 .

Total synthesis of chiriquitoxin, an analogue of tetrodotoxin isolated from the skin of a dart frog.

M. Isobe, T. Nishikawa, R. Sakakibara, 2014, Chemistry.

A New Synthetic Route to the Skeleton of Saxitoxin, a Naturally Occurring Blocker of Voltage-Gated Sodium Channels

T. Nishikawa, Yusuke Sawayama, 2012 .

Synthesis of 5- and 8-deoxytetrodotoxin.

M. Yotsu-Yamashita, M. Isobe, T. Nishikawa, 2014, Chemistry, an Asian journal.

Synthesis of tetrodotoxin, a classic but still fascinating natural product.

M. Isobe, T. Nishikawa, 2013, Chemical record.

An improved synthesis of (-)-5,11-dideoxytetrodotoxin.

M. Isobe, T. Nishikawa, M. Adachi, 2013, The Journal of organic chemistry.

An efficient total synthesis of optically active tetrodotoxin.

D. Urabe, M. Isobe, T. Nishikawa, 2004, Angewandte Chemie.

Total syntheses of 11-deoxytetrodotoxin and 8,11-dideoxytetrodotoxin

D. Urabe, M. Isobe, T. Nishikawa, 2003 .

Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, unnatural analogue of puffer fish toxin.

D. Urabe, M. Isobe, T. Nishikawa, 2004, Organic letters.

Asymmetric total synthesis of 11-deoxytetrodotoxin, a naturally occurring congener.

M. Isobe, T. Nishikawa, Masanori Asai, 2002, Journal of the American Chemical Society.

Synthesis of a common key intermediate for (−)-tetrodotoxin and its analogs

N. Yamamoto, M. Isobe, T. Nishikawa, 2001 .

STEREOELECTRONIC AND STERIC EFFECTS FOR CRITICAL OXIDATION TO THE CYCLOHEXANE DERIVATIVES FOR AN INTERMEDIATE TO (-)-TETRODOTOXIN

M. Isobe, T. Nishikawa, M. Bamba, 1998 .

Tin-assisted cyclization for chiral cyclohexane synthesis, an alternative route to (−)-tetrodotoxin skeleton

M. Isobe, T. Nishikawa, M. Bamba, 1996 .

Synthetic studies on a stereochemically complex natural product: designs for the total synthesis of (-)-tetrodotoxin

M. Isobe, T. Nishikawa, T. Goto, 1987 .

Synthesis of Dibromo Compounds Containing 2,6-Dioxabicyclo[3.1.1]heptane Similar to Core Moiety of Thromboxane A2

T. Nishikawa, Atsuo Nakazaki, Yoshihiko Nokura, 2018 .

Synthesis of Crambescin B Carboxylic Acid (I), a Potent Inhibitor of Voltage-Gated Sodium Channels.

M. Yotsu-Yamashita, T. Nishikawa, Atsuo Nakazaki, 2014 .

Synthesis of tetrodotoxin, a classic but still fascinating natural product.

M. Isobe, T. Nishikawa, 2013, Chemical record.

Biological activity of 8,11-dideoxytetrodotoxin: lethality to mice and the inhibitory activity to cytotoxicity of ouabain and veratridine in mouse neuroblastoma cells, Neuro-2a.

M. Yotsu-Yamashita, D. Urabe, M. Isobe, 2003, Toxicon : official journal of the International Society on Toxinology.

Bromocyclization of AlkynylGuanidine: A New Approach to the Synthesis of Cyclic Guanidinesof Saxitoxin

T. Nishikawa, Yusuke Sawayama, 2011 .

Synthesis of a α-C-Mannosyltryptophan Derivative, Naturally Occurring C-Glycosyl Amino Acid Found in Human Ribonuclease

T. Nishikawa, 1999 .

Syntheses of Naturally Occurring Terphenyls and Related Compounds

H. Kawagishi, M. Isobe, T. Nishikawa, 2006, Bioscience, biotechnology, and biochemistry.

Synthetic studies and biosynthetic speculation on marine alkaloid chartelline.

M. Isobe, T. Nishikawa, Shigeo Kajii, 2008, Chemical communications.

Synthesis and biological evaluation of both enantiomers of dynemicin a model compound

T. Jomori, M. Isobe, T. Nishikawa, 1995 .

Stereocontrolled synthesis and reactivity of sugar acetylenes

M. Isobe, T. Nishikawa, S. Hosokawa, 1999 .

Diastereoselective synthesis of 3,3-disubstituted oxindoles from atropisomeric N -aryl oxindole derivatives

T. Nishikawa, Susumu Kobayashi, Atsuo Nakazaki, 2012 .

Improved Syntheses of (+)-Iridomyrmecin and (-)-Isoiridomyrmecin, Major Components of Matatabilactone.

T. Nishikawa, M. Adachi, Yuki Miyazawa, 2016, Natural product communications.

Synthesis of chiral cyclohexanes from levoglucosenone and its application to an indole alkaloid reserpine

M. Isobe, T. Nishikawa, N. Fukami, 1987 .

Structural Study on a Naturally Occurring Terphenyl Quinone

B. Yingyongnarongkul, T. Nishikawa, Atsuo Nakazaki, 2013, Bioscience, biotechnology, and biochemistry.

Brønsted base and acid catalysts, and additional topics

T. Hashimoto, P. Schreiner, M. Klussmann, 2012 .

Stereocontrolled total synthesis of polygalolide A.

M. Isobe, T. Nishikawa, M. Adachi, 2013, Chemistry, an Asian journal.

Total synthesis of polygalolide A.

M. Isobe, T. Nishikawa, M. Adachi, 2011, Organic letters.

Total Synthesis of α-C-Mannosyltryptophan, a Naturally Occurring C-Glycosyl Amino Acid

M. Isobe, T. Nishikawa, Kyoko Wada, 2001 .

Hydrosilylation of acetylenes with catalytic biscobalthexacarbonyl complex and its application to heteroconjugate addition methodology

M. Isobe, T. Nishikawa, K. Yoza, 1999 .

Synthesis of a α-C-Mannosyltryptophan Derivative, Naturally Occurring C-Glycosyl Amino Acid Found in Human Ribonuclease.

M. Isobe, T. Nishikawa, M. Ishikawa, 1999 .

A novel stereoselective carbon-chain extension reaction at the C-6 position of 1,6-anhydropyranose

M. Isobe, T. Nishikawa, Norio Ohyabu, 2004 .

Stereocontrolled synthesis of the oxathiabicyclo[3.3.1]nonane core structure of tagetitoxin.

T. Nishikawa, M. Adachi, Hitomi Yamada, 2013, Chemical communications.

Biosynthesis of Indole Diterpene Lolitrems: Radical‐Induced Cyclization of an Epoxyalcohol Affording a Characteristic Lolitremane Skeleton

A. Minami, K. Miyamoto, J. Maruyama, 2020, Angewandte Chemie.

Biosynthesis of Indole Diterpene Lolitrems: Radical-Induced Cyclization of an Epoxyalcohol Affording a Characteristic Lolitremane Skeleton.

A. Minami, K. Miyamoto, J. Maruyama, 2020, Angewandte Chemie.

Semi‐synthesis and Structure–Activity Relationship of Neuritogenic Oleanene Derivatives

T. Nishikawa, Atsuo Nakazaki, J. Qi, 2018, ChemMedChem.

Biomimetic Synthesis and Structural Revision of Chaxine B and Its Analogues.

H. Kawagishi, T. Nishikawa, Atsuo Nakazaki, 2017, Organic letters.

Insight into the chemistry of cycloaddition between α-ketol oxylipin and epinephrine: isolation and structure elucidation of a new reaction product

N. Watanabe, T. Nishikawa, Ariaki Murata, 2013 .

Synthesis of Functionalized Cyclopentane for Pactamycin, a Potent Antitumor Antibiotic

D. Urabe, M. Isobe, T. Nishikawa, 2005 .

SYNTHESES OF N-ACYLISOXAZOLIDINE DERIVATIVES, RELATED TO A PARTIAL STRUCTURE FOUND IN ZETEKITOXIN AB, A GOLDEN FROG POISON

D. Urabe, M. Isobe, T. Nishikawa, 2009 .

One-Step Transformation of Trichloroacetamide into Isonitrile.

T. Nishikawa, M. Adachi, Tadachika Miyasaka, 2017, Organic letters.

Toward a Synthesis of Fawcettimine-Type Lycopodium Alkaloids: Stereocontrolled Synthesis of a Functionalized Azaspirocycle Precursor.

T. Nishikawa, Atsuo Nakazaki, Wen-Yu Huang, 2018, The Journal of organic chemistry.

Concise Synthesis of a Cyclopentane Intermediate Possessing All Nitrogen Functionalities for Pactamycin

T. Nishikawa, Atsuo Nakazaki, Nobuyuki Matsumoto, 2017, Synlett.

One‐Pot Synthesis of Haloacetylenes from Trimethylsilylacetylenes.

S. Shibuya, M. Isobe, T. Nishikawa, 1994 .

Concise Synthesis of Deformylflustrabromine, a Marine Indole Alkaloid, through a 2-Propynyl Dicobalt Hexacarbonyl Complex

M. Isobe, T. Nishikawa, Atsuo Nakazaki, 2011 .

A novel deprotection of trichloroacetamide

D. Urabe, M. Isobe, T. Nishikawa, 2004 .

Stereoelectronic and steric control in chiral cyclohexane synthesis toward (−)-tetrodotoxin

M. Isobe, T. Nishikawa, M. Bamba, 1998 .

Synthesis of an Advanced Intermediate Bearing Two Hydroxy Groups for (-)-Tetrodotoxin and Its Analogs

M. Isobe, T. Nishikawa, M. Adachi, 2010 .

Green spotted puffers detect a nontoxic TTX analog odor using crypt olfactory sensory neurons.

T. Nishikawa, H. Abe, Takehisa Suzuki, 2022, Chemical senses.

First Detection of Tetrodotoxins in the Cotylean Flatworm Prosthiostomum trilineatum

H. Sugita, T. Nishikawa, R. Suo, 2021, Marine drugs.

Changes in Tissue Distribution of Tetrodotoxin and Its Analogues in Association with Maturation in the Toxic Flatworm, Planocera multitentaculata

H. Sugita, N. Goto-Inoue, T. Nishikawa, 2022, Marine Biotechnology.

Tetrodotoxins in the flatworm Planocera multitentaculata.

H. Sugita, T. Nishikawa, Y. Kojima, 2022, Toxicon : official journal of the International Society on Toxinology.

Spiro Bicyclic Guanidino Compounds from Pufferfish: Possible Biosynthetic Intermediates of Tetrodotoxin in Marine Environments.

M. Yotsu-Yamashita, K. Konoki, T. Nishikawa, 2018, Chemistry.

Synthesis of 5,6,11-Trideoxytetrodotoxin

M. Isobe, T. Nishikawa, R. Sakakibara, 2014 .

Synthesis of the 8-Deoxy Analogue of 4,9-Anhydro-10-hemiketal-5-deoxy-tetrodotoxin, a Proposed Biosynthetic Precursor of Tetrodotoxin.

T. Nishikawa, M. Adachi, Tadachika Miyasaka, 2021, Organic letters.

Multifunctionality of the N-Trichloroacetyl Group Developed in the Synthesis of Tetrodotoxin, a Puffer Fish Toxin

D. Urabe, M. Isobe, T. Nishikawa, 2015, Synlett.

Scalable Synthesis of a NewDihydroxylated Intermediate for Tetrodotoxin and Its Analogues

H. Araki, M. Isobe, T. Nishikawa, 2010 .

One-pot non-enzymatic formation of firefly luciferin in a neutral buffer from p-benzoquinone and cysteine

Y. Oba, M. Ojika, T. Nishikawa, 2016, Scientific Reports.

Substituent Effect of Imino-O-arenesulfonates, a Coupling Partner in Suzuki-Miyaura Reaction for Substitution of the Pyrazine Ring : A Study for the Synthesis of Coelenterazine Analogs

M. Isobe, T. Nishikawa, M. Kuse, 2009 .

Dynamic chirality determines critical roles for bioluminescence in symplectin-dehydrocoelenterazine system.

N. Harada, C. Yu, M. Isobe, 2011, Chemistry, an Asian journal.

Pholasin luminescence is enhanced by addition of dehydrocoelenterazine.

T. Nishikawa, M. Kuse, Eiko Tanaka, 2008, Bioorganic & medicinal chemistry letters.

Selective protein modification by the hydroperoxide intermediate in a photoprotein, aequorin.

M. Isobe, T. Nishikawa, M. Kuse, 2009, Bioorganic & medicinal chemistry.

Substituent Effect of Imino‐O‐arenesulfonates, a Coupling Partner in Suzuki—Miyaura Reaction for Substitution of the Pyrazine Ring: A Study for the Synthesis of Coelenterazine Analogues.

M. Isobe, T. Nishikawa, M. Kuse, 2009 .

Dehydrocoelenterazine is the Organic Substance Constituting the Prosthetic Group of Pholasin

T. Nishikawa, M. Kuse, Eiko Tanaka, 2009, Chembiochem : a European journal of chemical biology.

Synthetic studies on antibiotic dynemicin A. Synthesis of cyclic enediyne model compound of dynemicin A

M. Isobe, T. Nishikawa, A. Ino, 1994 .

Synthesis of a Simple Model Compound of Dynemicin and Cycloaromatization with Pinacol-Pinacolone Rearrangement in the Strained Enediyne Medium Ring.

M. Isobe, T. Nishikawa, T. Goto, 1991 .

Methodology for stereochemical control in bioactive natural product synthesis - new methods toward enediyne antitumor antibiotics

M. Isobe, T. Nishikawa, T. Goto, 1990 .

Cesium Fluoride Promoted Cyclization in the Synthesis of Enediyne Antibiotics1

S. Shibuya, M. Isobe, T. Nishikawa, 1994 .

Methodology for Stereochemical Control in Bioactive Natural Product Synthesis: New Methods Toward Enediyne Antitumor Antibiotics

M. Isobe, T. Nishikawa, T. Goto, 1991 .

Magnetic quenching of the emission intensities of HPO and SnH in hydrogen—oxygen flames

T. Nishikawa, I. Ogasawara, N. I. Wakayama, 1984 .

A new ring expansion for a chiral hexahydroazulene skeleton possessing an angular methyl group.

T. Nishikawa, M. Adachi, T. Komada, 2011, The Journal of organic chemistry.

Application of discrete Fourier transform to electron spin resonance spectral data

T. Nishikawa, K. Someno, 1975 .

One Pot Synthesis of Haloacetylenes from Trimethylsilylacetylenes

S. Shibuya, M. Isobe, T. Nishikawa, 1994 .

Identification of an Asexual Reproduction Inducer of Phytopathogenic and Toxigenic Fusarium.

H. Osada, Zhonghua Ma, T. Nishikawa, 2018, Angewandte Chemie.

Identification of an Asexual Reproduction Inducer of Phytopathogenic and Toxigenic Fusarium

Zhonghua Ma, T. Nishikawa, Lan Xiang, 2018, Angewandte Chemie.

Total synthesis and biological evaluation of oscillatoxin D, E, and F.

K. Irie, T. Nishikawa, Atsuo Nakazaki, 2021, Bioscience, biotechnology, and biochemistry.

The Asymmetric Total Synthesis and Configuration Confirmation of Aplysiaenal and Nhatrangin A, Truncated Derivatives of Aplysiatoxin and Oscillatoxin.

T. Nishikawa, M. Kita, Mana Morishita, 2023, Journal of natural products.

Collective Synthesis of Aplysiatoxin/Oscillatoxin Analogues by a Bioinspired Strategy.

D. Urabe, T. Nishikawa, Yoshihiko Nokura, 2022, The Journal of organic chemistry.

Synthetic Studies on the Bicyclo[7.3.1]tridecenediyne System in an Antitumor Antibiotic, Dynemicin A

M. Isobe, T. Nishikawa, T. Goto, 1991 .

Treatment of eczema herpeticum with oral acyclovir.

M. Niimura, T. Nishikawa, 1988, The American journal of medicine.

The ESR of Alkyl Phenyl Nitroxide Radicals Studied as Hindered Rotation

T. Nishikawa, K. Someno, 1974 .

A New Deprotection Procedure of MTM Ether

T. Nishikawa, R. Sakakibara, M. Adachi, 2014, Synlett.

Stereocontrolled Synthesis of (-)-5,11-Dideoxytetrodotoxin.

Yamamoto, T. Nishikawa, Norio Ohyabu, 1999, Angewandte Chemie.

A synthetic route to the saxitoxin skeleton: synthesis of decarbamoyl α-saxitoxinol, an analogue of saxitoxin produced by the cyanobacterium Lyngbya wollei.

T. Nishikawa, Yusuke Sawayama, 2011, Angewandte Chemie.

Synthesis of Four Lysine-LinkedCereulide Analogues Showing Ionophoric Activity Towards PotassiumCations as Lead Compounds for Emetic Toxin-Detection by Immunoassays

M. Isobe, T. Nishikawa, A. Makarasen, 2009 .