S. Tanimori

Green synthesis of oxadiazolo[2,3-b]quinazolin-5-ones based on iodine-catalyzed cyclodesulfurization in water
20250 citationsauthor #2
Synthesis of Novel Imido-Substituted 1,4-Naphthoquinones and Benzoquinone Derivatives
20250 citationsauthor #4
Green Synthesis of 2‐Thioxo‐4‐quinazolinone Derivatives in Water
20234 citationsauthor #4
A quick and easy access to a series of thiocyanated enaminones and 2‐iminothiazolones using PIDA under mild conditions
20224 citationsauthor #2
Organic solvent-free synthesis of sulfonyl hydrazides in water
20226 citationsauthor #2
Access to γ-Carbolines: Synthesis of Isocryptolepine.
20213 citationsauthor #5
Proline‐catalyzed Transition‐Metal‐free Access to 1‐Substituted‐4‐Quinazolinones
20211 citationsauthor #4
Easy access to both enantiomers of 5-hydroxyequol and 3-(4-hydroxyphenyl)chroman-8-ol
20210 citationsauthor #3
A Facile Synthesis of 2-Aminobenzoxazines Based on IodineCatalyzed Desulfurative Cyclization
20212 citationsauthor #1
A Concise Enantiodivergent Synthesis of Equol
20204 citationsauthor #1
Chemical structure of hydrolysates of cereulide and their time course profile.
20201 citationsauthor #7
Total synthesis of ( S )‐(+)‐ ent ‐phomapyrones B and surugapyrone B
20205 citationsauthor #5
Enantio and diastereoselective total synthesis of all four stereoisomers of germicidin N
20205 citationsauthor #5
Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
20202 citationsauthor #1
Synthesis of the reported structure of homocereulide and its vacuolation assay.
20197 citationsauthor #6
Dataset on Chemical structure of hydrolysates of cereulide and their time course profile
20190 citationsauthor #6
Determining the suitability of a polar organic chemical integrated sampler (POCIS) for the detection of pesticide residue in the Ishikawa River and its tributary in Osaka, Japan.
201812 citationsauthor #5
Mechanistic study of silica-gel or FeCl3-promoted ring-opening aromatization of 7-oxanorborna-2,5-dienes affording 2-bromo-3-hydroxybenzoate derivatives
20180 citationsauthor #6
A rapid access to substituted oxazoles via PIFA-mediated oxidative cyclization of enamides
20178 citationsauthor #3
Sequential Synthesis, Olfactory Properties, and Biological Activity of Quinoxaline Derivatives
201726 citationsauthor #6
Facile Synthesis of Phenanthridinone Alkaloids via Suzuki–Miyaura Cross‐coupling
201711 citationsauthor #3
Copper-catalyzed tandem reaction directed toward synthesis of 2,2-disubstituted quinazolinones from vinyl halides and 2-aminobenzamides
20179 citationsauthor #4
A facile and rapid access to resveratrol derivatives and their radioprotective activity.
201611 citationsauthor #5
Oxone-mediated facile access to substituted pyrazoles
201629 citationsauthor #4
Temperature dependence on the pesticide sampling rate of polar organic chemical integrative samplers (POCIS)
201632 citationsauthor #8
Oxone‐Mediated Facile Access to Substituted Pyrazoles.
20160 citationsauthor #4
Proline-Mediated Transition Metal-Free Access to 1H-Indazolones from 2-Halobenzohydrazides.
201621 citationsauthor #3
Facile Access to 1H‐Indazoles Through Iodobenzene‐Catalyzed C—H Amination under Mild, Transition‐Metal‐Free Conditions.
20150 citationsauthor #3
One-pot synthesis of 3-hydroxyanthranilate derivatives using furans, bromoalkyne, and secondary amines
20157 citationsauthor #6
Silica Gel-Promoted Convenient Synthesis of 2-Bromo-3-hydroxybenzoate Derivatives.
20150 citationsauthor #5
One‐Pot Synthesis of 3‐Hydroxyanthranilate Derivatives Using Furans, Bromoalkyne, and Secondary Amines.
20150 citationsauthor #6
Synthesis and in vitro evaluation of thiododecaborated α, α- cycloalkylamino acids for the treatment of malignant brain tumors by boron neutron capture therapy
201420 citationsauthor #12
Regioselective Monoarylation of 2-Phenylbenzimidazole via Ruthenium-Catalyzed C–H Bond Functionalization
201411 citationsauthor #5
Silica gel-promoted convenient synthesis of 2-bromo-3-hydroxybenzoate derivatives
20147 citationsauthor #5
Efficient synthesis of useful heterocycles via transition metal-catalyzed cascade processes
20146 citationsauthor #1
Synthesis and in vitro evaluation of thiododecaborated α, α- cycloalkylamino acids for the treatment of malignant brain tumors by boron neutron capture therapy
20140 citationsauthor #12
Facile Access to 1H‐Indazoles through Iodobenzene‐Catalyzed C–H Amination under Mild, Transition‐Metal‐Free Conditions
201432 citationsauthor #3
Resveratrol inhibits hypoxia-inducible factor-1α-mediated androgen receptor signaling and represses tumor progression in castration-resistant prostate cancer.
201437 citationsauthor #3
Synthesis and Evaluation of Thiododecaborated α, α-Cycloalkyl Amino Acids for Boron Neutron Capture Therapy
20130 citationsauthor #11
Identification of carbonyl reductase 1 as a resveratrol-binding protein by affinity chromatography using 4'-amino-3,5-dihydroxy-trans-stilbene.
201322 citationsauthor #5
A Convenient One-Pot Access to Phenanthridinones via Suzuki—Miyaura Cross-Coupling Reaction
20131 citationsauthor #5
A convenient one-pot access to phenanthridinones via Suzuki–Miyaura cross-coupling reaction
201316 citationsauthor #5
Proline Catalyzes Direct C—H Arylations of Unactivated Arenes.
20130 citationsauthor #5
A General and Convenient Synthesis of Cereulide and Homocereulide, Macrocyclic Depsipeptides Isolated from Bacillus cereus
20130 citationsauthor #6
A Novel Modification Method of Peptides and Proteins by Anionic Dodecaborate Cage in Water
20120 citationsauthor #10
Dodecaborate-Containing L-Amino Acids as New Boron Carriers for Boron Neutron Capture Therapy
20120 citationsauthor #10
Proline catalyzes direct C-H arylations of unactivated arenes.
201290 citationsauthor #5
Copper-catalyzed synthesis of substituted indazoles from 2-chloroarenes at low catalyst-loading.
201228 citationsauthor #1
Biological evaluation of dodecaborate-containing L-amino acids for boron neutron capture therapy.
201254 citationsauthor #9
Characterization of D-galacturonate reductase purified from the psychrophilic yeast species Cryptococcus diffluens.
20119 citationsauthor #3
A General and Practical Access to Chiral Quinoxalinones with Low Copper-Catalyst Loading.
20110 citationsauthor #1
Synthesis of optically active dodecaborate-containing L-amino acids for BNCT.
201123 citationsauthor #5
A General and Practical Access to Chiral Quinoxalinones with Low Copper‐Catalyst Loading
201039 citationsauthor #1
Synthesis of novel quinoxaline derivatives and its cytotoxic activities.
200956 citationsauthor #1
Synthesis of cinnamyl-sesamol derivatives
20097 citationsauthor #1
Copper-Catalyzed Mild and EfficientEntry to 1-Substituted Indazolones
200822 citationsauthor #1
Copper‐Catalyzed Mild and Efficient Entry to 1‐Substituted Indazolones.
20081 citationsauthor #1
Palladium-catalyzed approach to substituted dihydrofurans, cyclopenta[b]furans and tetrahydrobenzofurans
20073 citationsauthor #1
Copper-Catalyzed α-Enolate Arylation Route to 2,3-Disubstituted Indoles
20070 citationsauthor #1
Palladium-Catalyzed Approach to Substituted Dihydrofurans, Cyclopenta[b]furans and Tetrahydrobenzofurans.
20070 citationsauthor #1
Copper-Catalyzed Synthesis of 2,3-Disubstituted Indoles.
20070 citationsauthor #1
Copper‐Catalyzed Synthesis of 2,3‐Disubstituted Indoles
200741 citationsauthor #1
Enzymatic Synthesis of Hydroxycinnamic Acid Glycerol Esters Using Type A Feruloyl Esterase from Aspergillus niger
200730 citationsauthor #3
Identification of phenolic compounds isolated from pigmented rices and their aldose reductase inhibitory activities
2007347 citationsauthor #2
STRUCTURE DETERMINATION AND STRUCTURE-ACTIVITY RELATIONSHIPS
20060 citationsauthor #4
Simple Preparation of New Functionalized Furan Derivatives via Sequential C—C and C—O Bond Formation Mediated by Palladium-Phosphine Catalyst.
20060 citationsauthor #1
Simple Preparation of New Functionalized Furan Derivatives via Sequential C-C and C-O Bond Formation Mediated by Palladium-Phosphine Catalyst
200613 citationsauthor #1
Synthesis of a New Proline-Derived Organic Catalyst and Its Evaluation for Direct Aldol Reaction.
20050 citationsauthor #1
An efficient construction of bridged chiral tetracyclic indolidines, a core structure of asperparaline, via stereocontrolled catalytic Pauson–Khand reaction
200513 citationsauthor #1
Palladium-Catalyzed One-Step Preparation of Novel Tricyclic Phenoxazine, Phenazine, and Dioxine Derivatives
20045 citationsauthor #1
Synthesis of a New Proline‐Derived Organic Catalyst and Its Evaluation for Direct Aldol Reaction
200427 citationsauthor #1
A Simple and Easy Access to 3-N-Alkyl-5-vinyloxazolidinones Mediated by Palladium—Phosphine Catalysts.
20030 citationsauthor #1
A simple and easy access to 3-N-alkyl-5-vinyloxazolidinones mediated by palladium-phosphine catalysts
20038 citationsauthor #1
Enantioselective Synthesis of Both Enantiomers of Dimethyl cis-(4-Acetoxycyclopent-2-enyl)malonate, Key Intermediates for Epijasmonate
20021 citationsauthor #1
An efficient chemical synthesis of nicotinamide riboside (NAR) and analogues.
200229 citationsauthor #1
A New Pathway to Chiral Tetracyclic Indolidines via Pauson—Khand Reaction.
20010 citationsauthor #1
A new pathway to chiral tetracyclic indolidines via Pauson–Khand reaction
200118 citationsauthor #1
Kinetic analysis of the reaction catalyzed by chitinase A1 from Bacillus circulans WL‐12 toward the novel substrates, partially N‐deacetylated 4‐methylumbelliferyl chitobiosides
200024 citationsauthor #2
Easy Access to Both Enantiomers of C7—C12 Segment of Epothilones.
20000 citationsauthor #1
Novel Palladium-Catalyzed Oxazolidone Synthesis.
20000 citationsauthor #1
Synthesis of the Spirosuccinimide Moiety of Asperparaline A
20007 citationsauthor #1
Chemo- and enzymatic synthesis of partially and fully N-deacetylated 4-methylumbelliferyl chitobiosides: fluorogenic substrates for chitinase.
20009 citationsauthor #2
Novel palladium-catalyzed oxazolidone synthesis
200019 citationsauthor #1
Easy Access to Both Enantiomers of C7-C12 Segment of Epothilones
19991 citationsauthor #1
Enantioselective Construction of Alicyclic Bicyclo[3.1.0]hexane Framework by Double Stereodifferentiation and Its Application for the Synthesis of Both Enantiomers of Vitamin D3 CD Ring Synthons.
19980 citationsauthor #2
Simple Synthesis of Both Enantiomers of the C7-C12 Segment of Epothilones.
19982 citationsauthor #1
Biological Activity of Hydroxo-vitamin B12 Degradation Product Formed during Microwave Heating
199822 citationsauthor #9
A Simple Divergence from Asymmetric Cyclopropane to Lactone Annulation.
19970 citationsauthor #2
A Concise Enantioselective Pathway to Carbocyclic Nucleoside: Asymmetric Synthesis of Carbocyclic Moiety of Carbovir
199710 citationsauthor #1
A Concise Enantioselective Pathway to Carbocyclic Nucleoside: Asymmetric Synthesis of Carbocyclic Moiety of Carbovir.
19970 citationsauthor #1
A SIMPLE DIVERGENCE FROM ASYMMETRIC CYCLOPROPANE TO LACTONE ANNULATION
199738 citationsauthor #2
Enantioselective construction of alicyclic bicyclo[3.1.0]hexane framework by double stereodifferentiation and its application for the synthesis of both enantiomers of vitamin D3 CD ring synthons
199711 citationsauthor #2
Studies Directed Toward the Synthesis of Macrolactins: Asymmetric Synthesis of C3-C9 and C17-C24 Subunits of Macrolactin A
199617 citationsauthor #1
Studies Directed Towards the Synthesis of Macrolactins: Asymmetric Synthesis of C3-C9 and C17-C24 Subunits of Macrolactin A.
19960 citationsauthor #1
A new nucleophilic ring opening of an activated cyclopropane and a formal synthesis of (+/-)-carbovir.
199510 citationsauthor #1
Nisamycin, a New Manumycin Group Antibiotic from Streptomyces sp. K106. Part 2. Structure Determination and Structure‐Activity Relationships.
19951 citationsauthor #4
Homoconjugate Addition of Organocuprate to Activated Cyclopropane and Its Application to the Synthesis of (±)-Juvabione
19952 citationsauthor #2
Efficient Chemical Conversion of (±)-Chokol G to (±)-Chokols A, B, C, F, and K, Chokolic Acid B, and Chokolal A
19944 citationsauthor #1
Nisamycin, a new manumycin group antibiotic from Streptomyces sp. K106. II. Structure determination and structure-activity relationships.
199413 citationsauthor #4
Stereoselective synthesis of (±)-5-(1-benzyloxyethyl)-6-(2-tert-butyldiphenyloxyethyl)-2-piperidinone: a formal total synthesis of thienamycin
19943 citationsauthor #1

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