T. Yokomatsu

发表

Acid sphingomyelinase inhibition suppresses lipopolysaccharide‐mediated release of inflammatory cytokines from macrophages and protects against disease pathology in dextran sulphate sodium‐induced colitis in mice

R. Eyanagi, S. Shibuya, S. Soeda, 2007, Immunology.

Inhibition of lipopolysaccharide-induced release of interleukin-8 from intestinal epithelial cells by SMA, a novel inhibitor of sphingomyelinase and its therapeutic effect on dextran sulphate sodium-induced colitis in mice.

S. Shibuya, S. Soeda, A. Sakata, 2007, Cellular immunology.

Effect of a-strain on a synthesis of cis-fused 4a-aryloctahydro-1H-cyclopenta[c]pyridine derivatives through tandem radical cyclisation of an α-acylamino–polyene system

S. Shibuya, K. Asami, T. Yokomatsu, 1986 .

Asymmetric synthesis of β-amino-α-hydroxyphosphinic acid derivatives through hydrophosphinylation of α-amino aldehydes

T. Yamagishi, S. Shibuya, T. Yokomatsu, 2002 .

Diastereoselective synthesis of chiral β-amino-α-hydroxy- H -phosphinates through hydrophosphinylation of α-amino aldehydes

T. Yamagishi, S. Shibuya, T. Yokomatsu, 2001 .

Asymmetric synthesis of phosphonic acid analogues for acylcarnitine

T. Yamagishi, S. Shibuya, K. Fujii, 2006 .

An attempt to promote neo‐vascularization by employing a newly synthesized inhibitor of protein tyrosine phosphatase

S. Koyanagi, S. Shibuya, S. Soeda, 2002, FEBS letters.

One-pot synthesis of 1,2,3-triazoles from boronic acids in water using Cu(II)-β-cyclodextrin complex as a nanocatalyst.

B. Kaboudin, T. Yokomatsu, Yaghoub Abedi, 2012, Organic & biomolecular chemistry.

Antiproliferative Activity of Purine Nucleoside Phosphorylase Multisubstrate Analogue Inhibitors Containing Difluoromethylene Phosphonic Acid against Leukaemia and Lymphoma Cells

A. Bzowska, L. Glavaš-Obrovac, Mariko Hashimoto, 2010, Chemical biology & drug design.

Stereoselective Reduction of Cyclopropylalkaones Possessing a Difluoromethylenephosphonate Group at the Ring: Application to Stereoselective Synthesis of Novel Cyclopropane Nucleotide Analogues

T. Yamagishi, H. Abe, S. Shibuya, 2000 .

Enantioselective synthesis of α-hydroxyphosphinic acid derivatives through hydrophosphinylation of aldehydes catalyzed by Al-Li-BINOL complex

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1999 .

Asymmetric dihydroxylation of 1-acyloxy-2(E)-alkenylphosphonates with AD-mix reagents. Effects of 1-acyloxy functional groups on the asymmetric dihydroxylation

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1998 .

Diastereoselective synthesis of ω-phosphonic acid analogues of 4-arylkainoids

S. Shibuya, T. Yokomatsu, Y. Yuasa, 1998 .

Syntheses of Dibenzo [b, g] azecines and Dibenzo [b, f] azonines

S. Shibuya, T. Yokomatsu, S. Kano, 1975 .

Stereoselective Synthesis of Natural Products via Cationic and Radical Intermediates

S. Shibuya, T. Yokomatsu, Y. Yuasa, 1993 .

Discovery of non-competitive thrombin inhibitor derived from competitive tryptase inhibitor skeleton: Shift in molecular recognition resulted from skeletal conversion of carboxylate into phosphonate.

Y. Hashimoto, Ryosuke Ijuin, H. Aoyama, 2015, Bioorganic & medicinal chemistry letters.

Interactions of Potent Multisubstrate Analogue Inhibitors with Purine Nucleoside Phosphorylase from Calf Spleen—Kinetic and Spectrofluorimetric Studies

A. Bzowska, S. Shibuya, T. Yokomatsu, 2003, Nucleosides, nucleotides & nucleic acids.

Synthesis of acyclic nucleotide analogues possessing a difluoromethylene phosphonyl group at the side chain

S. Shibuya, T. Yokomatsu, Y. Yuasa, 2003 .

Lipase-catalyzed enantioselective acylation of prochiral 2-(ω-phosphono)alkyl-1,3-propanediols: Application to the enantioselective synthesis of ω-phosphono-α-amino acids

S. Shibuya, T. Yokomatsu, Mutsumi Sato, 1996 .

Synthesis of 2-substituted 3,5-dibromothiophenes through base-catalyzed halogen dance reaction of 2,5-dibromothiophene

S. Shibuya, T. Yokomatsu, S. Kano, 1983 .

One-pot synthesis of alkoxyamine derivatives by reductive alkoxyamination with a 2-picoline-borane complex

T. Yamagishi, T. Nakata, T. Yokomatsu, 2009 .

CuSO4-Mediated Homocouplingof Arylboronic Acids under Ligand- and Base-Free Conditions in Air

B. Kaboudin, T. Yokomatsu, T. Haruki, 2011 .

Novel strategy for synthesis of substituted benzimidazo[1,2-a]quinolines.

Ryosuke Ijuin, H. Aoyama, T. Yokomatsu, 2013, Organic letters.

New 1,2-transpositions and alkylative 1,2-transpositions of a carbonyl group

S. Hibino, S. Shibuya, T. Yokomatsu, 1978 .

Stereoselective C-Glycosylation of 2,3-Dideoxyribofuranosides Controlled by the Methylenephosphonothioate Functional Groups at the 3-Position

Takanori Shimizu, S. Shibuya, T. Yokomatsu, 2000 .

Stereoselective β-N-glycosylation of 2,3-dideoxyribofuranose derivatives controlled by a methylenephosphonothioate functional group at the 3-position

Takanori Shimizu, S. Shibuya, T. Yokomatsu, 1998 .

Enantioselective synthesis of α-hydroxyphosphonates throughasymmetric Pudovik reactions with chiral lanthanoid and titaniumalkoxides

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1997 .

Stereoselective Synthesis of .beta.-Oxygenated .alpha.-Hydroxyphosphonates by Lewis Acid-Mediated Stereoselective Hydrophosphonylation of .alpha.-Benzyloxy Aldehydes. An Application to the Synthesis of Phosphonic Acid Analogs of Oxyamino Acids

S. Shibuya, T. Yokomatsu, Y. Yoshida, 1994 .

Stereoselective Synthesis of β-Oxygenated α- Hydroxyphosphonates by Lewis Acid-Mediated Stereoselective Hydrophosphonylation of α-Benzyloxy Aldehydes. An Application to the Synthesis of Phosphonic Acid Analogues of Oxyamino Acids.

S. Shibuya, T. Yokomatsu, Y. Yoshida, 1995 .

Enantioselective synthesis of α-amino phosphonic acids by an application of stereoselective opening of homochiral dioxane acetals with triethyl phosphite

S. Shibuya, T. Yokomatsu, 1992 .

Diastereoselective addition of α-substituted α-amino-H-phosphinates to imines using Yb(OTf)3 as an efficient Lewis acid catalyst

T. Yamagishi, B. Kaboudin, T. Yokomatsu, 2007 .

Resolution of Racemic α-Hydroxyphosphonates: Bi(OTf)3-Catalyzed Stereoselective Esterification of α-Hydroxyphosphonates with (+)-Dibenzoyl-l-tartaric Anhydride

H. Aoyama, B. Kaboudin, T. Yokomatsu, 2019, ACS omega.

Resolution of enantiomers of novel C2 -symmetric aminobisphosphinic acids via diastereomeric salt formation with quinine.

M. R. Faghihi, B. Kaboudin, T. Yokomatsu, 2015, Chirality.

A novel and simple method for the preparation of (R)- and (S)-pyrrolidine-2-phosphonic acids: phosphonic acid analogues of proline

H. Aoyama, B. Kaboudin, T. Yokomatsu, 2013 .

A catalyst-free, three-component decarboxylative coupling of amino acids with aldehydes and H-dialkylphosphites for the synthesis of α-aminophosphonates

H. Aoyama, L. Karami, B. Kaboudin, 2013 .

A chemo-enzymatic synthesis of optically active 1,1-diethoxyethyl(aminomethyl)phosphinates: useful chiral building blocks for phosphinyl dipeptide isosteres

T. Yamagishi, T. Yokomatsu, T. Haruki, 2011 .

CuII–β‐Cyclodextrin Complex as a Nanocatalyst for the Homo‐ and Cross‐Coupling of Arylboronic Acids under Ligand‐ and Base‐Free Conditions in Air: Chemoselective Cross‐Coupling of Arylboronic Acids in Water

B. Kaboudin, T. Yokomatsu, Yaghoub Abedi, 2011 .

First resolution of ( R , R )- and ( S , S )-bis(1-hydroxyphenylmethyl)phosphinic acids via diastereomeric salt formation with enantiopure 1-phenylethylamines

B. Kaboudin, T. Yokomatsu, H. Haghighat, 2008 .

One-pot synthesis of biologically active 1,2,3-trisubstituted pyrrolo[2,3-b]quinoxalines through a palladium-catalyzed reaction with internal alkyne moieties

A. Yoshida, Ali Keivanloo, B. Kaboudin, 2018, Molecular Diversity.

Regioselective synthesis of 2,3-disubstituted 1-alkyl pyrrolo[2,3-b] quinoxalines through palladium-catalyzed Heck reaction of chalcones and evaluation of their anti-bacterial activities

A. Yoshida, Ali Keivanloo, B. Kaboudin, 2018 .

Enantioselective synthesis of threo-α,β-dihydroxyphosphonates by asymmetric dihydroxylation of vinylphosphonates. An application to the stereocontrolled synthesis of (4S,5S)-4-diethylphosphono-5-hydroxymethyl-2,2-dimethyl-1,3-dioxolane

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1995 .

Enantioselective hydrophosphonylation of aromatic aldehydes catalyzed by chiral titanium alkoxides

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1993 .

Enantioselectivity for hydrophosphonylation of aromatic aldehydes catalyzed by lanthanum binaphthol complex. Remarkable electronic effect of aromatic substituents

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1993 .

Fe3O4 nanoparticle-supported Cu(II)-β-cyclodextrin complex as a magnetically recoverable and reusable catalyst for the synthesis of symmetrical biaryls and 1,2,3-triazoles from aryl boronic acids

B. Kaboudin, T. Yokomatsu, Ramin Mostafalu, 2013 .

Analysis of Binding Interaction between N,N-Bis (Phosphinomethyl) Amines as a New Class of 1-Aminophosphinic Acids and Bovine Serum Albumin Using Fluorescence Spectroscopy

M. R. Faghihi, B. Kaboudin, T. Yokomatsu, 2014, International Journal of Biochemistry and Biophysics.

Lipase-catalyzed kinetic resolution of α-hydroxy-H-phosphinates

T. Yamagishi, S. Shibuya, T. Yokomatsu, 2004 .

Enantioselective Synthesis of α‐Hydroxyphosphonates Through Asymmetric Pudovik Reactions with Chiral Lanthanoid and Titanium Alkoxides.

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1997 .

Enantioselective synthesis of threo-α,β-dihydroxyphosphonates by asymmetric dihydroxylation of 1(E)-alkenylphosphonates with AD-mix reagents

T. Yamagishi, Y. Yoshida, S. Shibuya, 1998 .

Stereodivergent synthesis of β-amino-α-hydroxyphosphonic acid derivatives by lewis acid mediated stereosclective hydrophosphonylation of α-amino aldehydes

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1993 .

Diastereoselective synthesis of β-substituted α-hydroxyphosphinates through hydrophosphinylation of α-heteroatom-substituted aldehydes

T. Yamagishi, S. Shibuya, B. Kaboudin, 2003 .

N-Glycosylation of 2,3-dideoxyfuranose derivatives having a (diethoxyphosphorothioyl)difluoromethyl group at the 3α-position

S. Shibuya, T. Yokomatsu, Y. Yuasa, 2003 .

Stereoselective synthesis of highly-functionalized cyclohexene derivatives having a diethoxyphosphoryldifluoromethyl functionality from cyclohex-2-enyl-1-phosphates

S. Shibuya, C. Sakuma, T. Yokomatsu, 2003 .

Synthesis of non-competitive inhibitors of sphingomyelinases with significant activity.

J. Koizumi, Y. Tsuji, S. Shibuya, 2003, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase.

S. Soeda, H. Shimeno, T. Yokomatsu, 2001, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases.

Y. Hayakawa, S. Koyanagi, S. Soeda, 2000, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. a new class of inhibitors for purine nucleoside phosphorylases.

Y. Hayakawa, S. Soeda, H. Shimeno, 1999, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of α, α-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B

S. Shibuya, S. Soeda, H. Shimeno, 1999 .

Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and the cyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase.

H. Abe, M. Sato, S. Soeda, 1998, Bioorganic & medicinal chemistry.

Synthesis of (2′S,3′S)-9-(4′-phosphono-4′,4′-difluoro-2′,3′-methanobutyl)guanine and its enantiomer. Evaluation of the inhibitory activity for purine nucleoside phosphorylase

H. Abe, S. Shibuya, S. Soeda, 1997 .

Facile synthesis of aryl(difluoromethyl)phosphonates through CuBr-mediated cross coupling reactions of [(diethoxyphosphinyl)difluoromethyl]zinc bromide with aryl iodides

S. Shibuya, T. Yokomatsu, K. Suemune, 1997 .

Synthesis of (alpha,alpha-Difluoroallyl)phosphonates from Alkenyl Halides or Acetylenes.

S. Shibuya, T. Yokomatsu, K. Suemune, 1996, The Journal of organic chemistry.

Stereocontrolled synthesis of hydroxymethylene phosphonate analogues of phosphorylated tyrosine and their conversion to monofluoromethylene phosphonate analogues

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1996 .

Stereoselective Synthesis of Methylenephosphonate Analogues of 2-Deoxyribose 3-Phosphates through Cyclization of Alkyl Radicals to Vinylphosphonates

Takanori Shimizu, S. Shibuya, T. Yokomatsu, 1995 .

Lipase-catalyzed kinetic resolution of cis-1-diethylphosphonomethyl-2-hydroxymethylcyclohexane. Application to enantioselective synthesis of 1-diethylphosphonomethyl-2-(5′-hydantoinyl)cyclohexane

S. Shibuya, T. Yokomatsu, Koji Matsumoto, 1995 .

Stereoselective Synthesis of γ,δ-Unsaturated α-Hydroxyphosphonates through [2,3]-Wittig Sigmatropic Rearrangement of α-Allyloxyphosphonates

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1995 .

Highly Regioselective Silylation of α,β-Dihydroxyphosphonates: An Application to Stereoselective Synthesis of α-Amino-β-hydroxyphosphonic Acid Derivatives

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1995 .

Catalyst-free Petasis-type reaction: Three-component decarboxylative coupling of boronic acids with proline and salicylaldehyde for the synthesis of alkylaminophenols

B. Kaboudin, T. Yokomatsu, F. Kazemi, 2018 .

Hydroxy-bisphosphinic acids: synthesis and complexation properties with transition metals and lanthanide ions in aqueous solution

M. R. Faghihi, H. Abdollahi, A. Ezzati, 2016, Journal of the Iranian Chemical Society.

Resolution of enantiomers of [α-hydroxy-(o-chlorophenyl)methyl]phosphinic acid via diastereomeric salt formation with enantiopure 1-phenylethylamines

B. Kaboudin, T. Yokomatsu, S. Alaie, 2011 .

Synthesis and Complexation Properties of N,N-Bis(phosphinomethyl)amine as a New Class of 1-Aminophosphinic Acids with Transition Metals and Lanthanide Ions in Aqueous Solution

H. Abdollahi, F. Saadati, B. Kaboudin, 2011 .

Diastereoselective synthesis of alpha,beta'-disubstituted aminomethyl(2-carboxyethyl)phosphinates as phosphinyl dipeptide isosteres.

T. Yamagishi, T. Yokomatsu, T. Haruki, 2008, Organic letters.

Diastereoselective Synthesis of Novel α-Amino-α′-hydroxyphosphinates by Hydrophosphinylation of α-Amino-H-phosphinates to Aldehydes

T. Yamagishi, B. Kaboudin, T. Yokomatsu, 2007 .

Diastereoselective alkylation of iminomethylenephosphinates possessing an asymmetric center at the phosphorus atom

T. Yamagishi, T. Yokomatsu, T. Haruki, 2006 .

A novel method for the separation of bis(alpha-hydroxyalkyl)phosphinic acid diastereoisomers via formation of novel cyclic phosphinic acids.

B. Kaboudin, T. Yokomatsu, H. Haghighat, 2006, The Journal of organic chemistry.

Simple and Efficient Method for Preparation of Conformationally Constrained Aminomethylene gem-Diphosphonate Derivatives via Beckmann Rearrangement

Y. Yoshida, S. Shibuya, T. Yokomatsu, 1994 .

A Safe and Scalable Procedure for Preparation of α-Picoline–Borane from Sodium Mono-acyloxyborohydrides and α-Picoline

T. Yamagishi, T. Nakata, Yoshinori Yamamoto, 2012 .

Diels-Alder cycloaddition of novel buta-1,-3-diene derivatives possessing a (diethoxyphosphinoyl)difluoromethyl unit.

T. Yokomatsu, S. Shibuya, S. Katayama, 2001, Chemical communications.

Enzymatic desymmetrization of prochiral 2-benzyl-1,3-propanediol derivatives: A practical chemoenzymatic synthesis of novel phosphorylated tyrosine analogues

S. Shibuya, T. Yokomatsu, T. Murano, 1998 .

Efficient synthesis of 2-phenyl-3-substituted furo/thieno[2,3-b]quinoxalines via Sonogashira coupling reaction followed by iodocyclization and subsequent palladium-catalyzed cross-coupling reactions

Ali Keivanloo, B. Kaboudin, T. Yokomatsu, 2016 .

A convenient and general procedure for the synthesis of α-ureidophosphonates under catalyst-free conditions

B. Kaboudin, T. Yokomatsu, Mohammad Bagher Afsharinezhad, 2011 .

Asymmetric synthesis of optically active α-substituted α-amino-H-phosphinates through resolution of 1,1-diethoxyethyl(aminomethyl)phosphinates

T. Yamagishi, T. Yokomatsu, T. Haruki, 2007 .

The kinetic study on the desulfurization of 4,5-trans and 4,5-cis-5-phenylthiooxazolidin-2-ones via cyclic carbamoyloxyradical species

S. Shibuya, T. Yokomatsu, S. Kano, 1990 .

Studies on the Reaction of Diimineswith Thiourea: Synthesis and Solvent-Induced cis/trans-Isomerizationof 1,3,5-Triazinane-2-thiones

B. Kaboudin, T. Yokomatsu, Tahereh Ghasemi, 2009 .

Diastereoselective synthesis of 2,3-cis-2-alkyl-3-oxygenated piperidine derivatives by titanium mediated intramolecular cyclization of α-aminoacetal-allylsilane system

H. Iwasawa, S. Shibuya, T. Yokomatsu, 1987 .

Asymmetric Synthesis of 2-Amino Alcohol Derivatives from (S)-α-Amino Aldehydes via Chiral Acetal Templates

H. Iwasawa, S. Shibuya, T. Yokomatsu, 1987 .

Highly enantioselective creation of quaternary carbons in a halolactonization of bis-γ,δ-unsaturated carboxylic imides derived from a camphorsultam: Enantioselective synthesis of (+)-mesembrine

H. Iwasawa, S. Shibuya, T. Yokomatsu, 1992 .

A simple and novel method for the direct conversion of carboxylic acids into thioamides

B. Kaboudin, T. Yokomatsu, Jun-ya Kato, 2013 .

Highly stereocontrolled synthesis of the four individual stereoisomers of statine

S. Shibuya, T. Yokomatsu, S. Kano, 1988 .

Reductive Alkylation of Hydrazine Derivatives with α-Picoline-Borane and Its Applications to the Syntheses of Useful Compounds Related to Active Pharmaceutical Ingredients

T. Yamagishi, T. Kataoka, T. Yokomatsu, 2014, Synthesis.

Studies on the Reaction of Diimines with Thiourea: Synthesis and Solvent‐Induced cis/trans‐Isomerization of 1,3,5‐Triazinane‐2‐thiones.

B. Kaboudin, T. Yokomatsu, Tahereh Ghasemi, 2010 .

A new and facile stereoselective synthesis of cis-4a-aryl-1,2,3,4,4a,5,6,8a-octahydroisoquinoline derivatives.

S. Shibuya, T. Yokomatsu, S. Kano, 1982 .

New synthetic design for formation of carbon-carbon triple bonds

S. Shibuya, T. Yokomatsu, S. Kano, 1978 .

Highly water-dispersible magnetite nanoparticle supported-palladium–β-cyclodextrin as an efficient catalyst for Suzuki–Miyaura and Sonogashira coupling reactions

B. Kaboudin, T. Yokomatsu, F. Kazemi, 2016 .

Diastereoconversion of 1-Alkynyl-2-aminoalkanols through Oxazoline-2-ones with SN2 Type Inversion of the Hydroxy Group

H. Iwasawa, T. Yokomatsu, S. Kano, 1988 .

Synthesis of 5-Aminobenzoimidazo[1,2-a]Quinoline Derivatives Through One-Pot Two-Step Cascade Reaction

Ryosuke Ijuin, H. Aoyama, T. Yokomatsu, 2016 .

Group IV-Metal-Catalyzed Aminolysis of N-Acyl-2-oxazolidinones: Applications to the Chemoselective and Enantioselective Carbonylation of Primary Alkylamines

S. Shibuya, T. Yokomatsu, A. Arakawa, 1994 .

Structural-based design and synthesis of novel 9-deazaguanine derivatives having a phosphate mimic as multi-substrate analogue inhibitors for mammalian PNPs.

A. Bzowska, Mariko Hashimoto, Sadao Hikishima, 2010, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of 9-deazaguanine derivatives connected by a linker to difluoromethylene phosphonic acid as multi-substrate analogue inhibitors of PNP.

A. Bzowska, Mariko Hashimoto, Sadao Hikishima, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of 9-(5',5'-difluoro-5'-phosphonopentyl)guanine derivatives for PNP-inhibitors.

S. Koyanagi, S. Shibuya, S. Soeda, 2006, Bioorganic & medicinal chemistry.

A Regio and Diastereoselective Bromolactamization of d,g-Unsaturaterd Thioimidates

H. Iwasawa, S. Shibuya, T. Yokomatsu, 1987 .

Radical-mediated furanose ring reconstruction from 2′,3′-seco-uridine

T. Miyasaka, S. Shibuya, T. Yokomatsu, 2001 .

A Diadtereoselective Synthesis of threo 2-(a-Hydroxyalkyl)piperdines via Oxacarbamoylinium Ion-(Z)-vinylsilane Cyclization

S. Shibuya, T. Yokomatsu, S. Kano, 1986 .

Diastereoselective synthesis of the Leu-Pro type phosphinyl dipeptide isostere.

T. Yamagishi, T. Yokomatsu, Naoko Tashiro, 2011, The Journal of organic chemistry.

Enantioselective Synthesis of α-Amino Phosphonic Acids by an Application of Stereoselective Opening of Homochiral Dioxane Acetals with Triethyl Phosphite.

S. Shibuya, T. Yokomatsu, 1992 .

Highly Diastereoselective Synthesis of (3R, 4R)- and (3R, 4S)-β, γ-Diamino Acids from D-Phenylalanine

H. Iwasawa, S. Shibuya, T. Yokomatsu, 1988 .

Recent Development of Efficient Synthesis for .ALPHA.-Heteroatom-substituted Phosphonates.

T. Yamagishi, S. Shibuya, T. Yokomatsu, 1995 .

Diastereoselective Addition of α-Substituted α-Amino-H-phosphinates to Imines Using Yb(OTf)3 as an Efficient Lewis Acid Catalyst.

T. Yamagishi, B. Kaboudin, T. Yokomatsu, 2007 .

Novel Method for the Synthesis of α-Amino-α′-hydroxyalkylphosphinic Acids and Bis(α-aminoalkyl)phosphinic Acids: Nuclephilic Addition of α-Hydroxy-H-phosphinic Acids to Diimines

B. Kaboudin, T. Yokomatsu, S. Alaie, 2012 .

Synthesis of a New Class of Phosphinic Acids: Synthesis of Novel Four-Membered Cyclic Oxaphosphetanes by Intramolecular Mitsunobu Reaction of Bis(α-hydroxyalkyl)phosphinic Acids

B. Kaboudin, T. Yokomatsu, H. Haghighat, 2011 .

Reaction of 1-Amino BisphosphinicAcids with Acid Chlorides: Synthesis of Novel Cyclic 1-Hydroxy-1′-amino-1,1-bisphosphinicAcids

F. Saadati, B. Kaboudin, T. Yokomatsu, 2010 .

Synthesis of a New Class of Phosphinic Acids: Synthesis of Novel Four-Membered Cyclic Oxaphosphetanes by Intramolecular Mitsunobu Reaction of Bis(α-hydroxyalkyl)phosphinic Acids.

B. Kaboudin, T. Yokomatsu, H. Haghighat, 2012 .

Reaction of 1‐Amino Bisphosphinic Acids with Acid Chlorides: Synthesis of Novel Cyclic 1‐Hydroxy‐1′‐amino‐1,1‐bisphosphinic Acids.

F. Saadati, B. Kaboudin, T. Yokomatsu, 2010 .

Copper(I) Iodide Catalyzed Synthesis of Thiophosphates by Coupling of H-Phosphonates with Benzenethiols

B. Kaboudin, T. Yokomatsu, Yaghoub Abedi, 2013 .

Nucleic Acids

L. Lankiewicz, A. Kozaki, T. Gotoh, 2007 .

An efficient diastereoselective synthesis of 6-hydroxy-4a-phenyl-cis-decahydroisoquinolines through N-acyliminium ion induced polyene cyclization

S. Shibuya, T. Yokomatsu, S. Kano, 1985 .

N-arylation of amines: C–N coupling of amines with arylboronic acids using Fe3O4 magnetic nanoparticles-supported EDTA–Cu(II) complex in water

B. Kaboudin, T. Yokomatsu, F. Kazemi, 2014 .

Small-molecular inhibitors of Ca²⁺-induced mitochondrial permeability transition (MPT) derived from muscle relaxant dantrolene.

Y. Hashimoto, M. Sodeoka, H. Aoyama, 2012, Bioorganic & medicinal chemistry.

Copper(I) Iodide Catalyzed Synthesis of Thiophosphates by Coupling of H-Phosphonates with Benzenethiols

B. Kaboudin, T. Yokomatsu, Yaghoub Abedi, 2013, Synthesis.

Elevation of de novo ceramide synthesis in tumor masses and the role of microsomal dihydroceramide synthase

S. Koyanagi, S. Shibuya, S. Soeda, 2003, International journal of cancer.

9‐Deazaguanine derivatives connected by a linker to difluoromethylene phosphonic acid are slow‐binding picomolar inhibitors of trimeric purine nucleoside phosphorylase

B. Wielgus-Kutrowska, Katarzyna Breer, A. Bzowska, 2010, The FEBS journal.

Inhibitory Properties of Nucleotides with Difluoromethylenephosphonic Acid as a Phosphate Mimic versus Calf Spleen Purine Nucleoside Phosphorylase and Effect of These Analogues on the Viability of Human Blood Lymphocytes

A. Bzowska, L. Glavaš-Obrovac, M. Suver, 2007, Nucleosides, Nucleotides & Nucleic Acids.

Synthesis of β-oxygenated α-amino acids and γ-oxygenated δ-amino acids from α-amino acids

S. Shibuya, T. Yokomatsu, Y. Yuasa, 1992 .

Calf spleen purine-nucleoside phosphorylase: crystal structure of the binary complex with a potent multisubstrate analogue inhibitor.

A. Bzowska, G. Koellner, Gertraud Koellner, 2004, Acta crystallographica. Section D, Biological crystallography.

Synthesis of β-Oxygenated γ-Amino Acids and γ- Oxygenated δ-Amino Acids from α-Amino Acids.

S. Shibuya, T. Yokomatsu, Y. Yuasa, 1992 .

Formation of indolo[l,2-a][3]benzazocine system from 1-halogenophenethyl-4,5-dihydro-3-2-benzazepine

T. Yokomatsu, S. Kano, 1978 .

Synthesis of Allenic (α,α-Difluoromethylene)phosphonates from Propargylic Tosylates and Acetates

S. Shibuya, T. Yokomatsu, Aiko Ichimura, 2001 .

1,3-Dipolar Cycloaddition of Diazomethane to 1,1-Difluoroallylphosphonates: Application to Synthesis of Cyclopropane Derivatives Having a Diethoxyphosphoryldifluoromethylene Unit

S. Shibuya, T. Yokomatsu, K. Suemune, 2002 .

A synthesis of simple 4,4-disubstituted tetrahydroisoquinolines by cyclization of α,α-disubstituted phenylacetamides

S. Shibuya, T. Yokomatsu, S. Kano, 1985 .

A practical synthesis of 8-hydroxyacyclovir and 9-(carboxymethoxymethyl)guanine, metabolites of acyclovir

T. Yamagishi, S. Shibuya, T. Yokomatsu, 2005 .

Pd(II)-β-cyclodextrin complex: Synthesis, characterization and efficient nanocatalyst for the selective Suzuki-Miyaura coupling reaction in water

B. Kaboudin, T. Yokomatsu, F. Kazemi, 2016 .

A facile and efficient stereoselective synthesis of 6-hydroxy-trans-4a-phenyldecahydroisoquinoline

S. Shibuya, T. Yokomatsu, S. Kano, 1983 .

1.45 A resolution crystal structure of recombinant PNP in complex with a pM multisubstrate analogue inhibitor bearing one feature of the postulated transition state.

B. Wielgus-Kutrowska, Katarzyna Breer, A. Bzowska, 2010, Biochemical and biophysical research communications.

A new synthetic approach to (+)-galantinic acid, degradation product from the peptide antibiotic galantin. I: Via 4-amino-3-hydroxypyranose

S. Shibuya, T. Yokomatsu, S. Kano, 1990 .

Synthesis of poly-substituted pyrazolo[1,5-a]quinolines through one-pot two component cascade reaction

Ryosuke Ijuin, H. Aoyama, T. Yokomatsu, 2014 .

EFFECT OF A-STRAIN. DIASTEREOSELECTIVE SYNTHESIS OF 3,2′-METHYLENE BRIDGED CIS-4a-ARYLDECAHYDROISOQUINOLINE RING SYSTEM VIA N-ACYLIMINIUM ION-POLYENE RING CLOSURE

S. Shibuya, T. Yokomatsu, S. Kano, 1986 .

Inhibition of sphingomyelinase activity helps to prevent neuron death caused by ischemic stress

Y. Tsuji, S. Shibuya, S. Soeda, 2004, Neurochemistry International.

N‐Arylation of Amines: C—N Coupling of Amines with Arylboronic Acids Using Fe3O4 Magnetic Nanoparticles‐Supported EDTA—Cu(II) Complex in Water.

B. Kaboudin, T. Yokomatsu, F. Kazemi, 2015 .

An efficient diastereoselective synthesis of 6-hydroxy-4a-[3,4-crowned(15-crown-5)phenyl]-trans-decahydroisoquinoline

S. Shibuya, T. Yokomatsu, S. Kano, 1985 .

General synthesis of oxirans

S. Shibuya, T. Yokomatsu, S. Kano, 1978 .

GENERAL SYNTHESIS OF OXIRANES

S. Shibuya, T. Yokomatsu, S. Kano, 1979 .

The Reaction of 1-Substituted Isoquinolines and 3H-2-Benzazepines with Dimsylsodium

S. Shibuya, T. Yokomatsu, S. Kano, 1977 .

Novel syntheses of dibenzo[d,f]azonine and dibenzo[e,g]azecine systems

S. Shibuya, T. Yokomatsu, S. Kano, 1974 .

Trimeric purine nucleoside phosphorylase: exploring postulated one-third-of-the-sites binding in the transition state.

B. Wielgus-Kutrowska, Katarzyna Breer, A. Bzowska, 2012, Bioorganic & medicinal chemistry.

A NEW GENERATION OF α-OXA-ACYLIMINIUM IONS AND AN APPLICATION TO A SYNTHESIS OF OXAZOLO[4,3,a]ISOQUINOLINE AND RELATED COMPOUNDS

S. Shibuya, T. Yokomatsu, S. Kano, 1983 .

Convenient Synthesis of Cyclopropylalkanol Derivatives Possessing a Difluoromethylenephosphonate Group at the Ring.

T. Yamagishi, H. Abe, S. Shibuya, 1999, The Journal of organic chemistry.

DIMSYLSODIUM-INDUCED REARRANGEMENT OF ALKYLIMIDATES TO N-ALKYLLACTAMS

S. Hibino, S. Shibuya, T. Yokomatsu, 1977 .

Overexpressed proteins may act as mops removing their ligands from the host cells: a case study of calf PNP.

B. Wielgus-Kutrowska, Katarzyna Breer, A. Bzowska, 2010, Biochemical and biophysical research communications.

A synthesis of oxazolo[4,3-a]isoquinoline and related compounds through intramolecular arylation of .alpha.-oxaacyliminium ions

S. Shibuya, T. Yokomatsu, S. Kano, 1983 .

A SYNTHESIS OF OXAZOLO(4,3-A)ISOQUINOLINE AND RELATED COMPOUNDS THROUGH INTRAMOLECULAR ARYLATION OF α-OXAACYLIMINIUM IONS

S. Shibuya, T. Yokomatsu, S. Kano, 1984 .

Aluminum-mediated one-pot conversion of α-amino acid esters to threo 2-amino alcohols with high diastereoselectivity

S. Shibuya, T. Yokomatsu, S. Kano, 1989 .

N-demethylation of dibenz[b,f]azonines with mercuric acetate.

T. Yokomatsu, S. Kano, T. Ebata, 1977 .

N-DEMETHYLATION OF DIBENZ(B,F)AZONINES WITH MERCURIC ACETATE

T. Yokomatsu, S. Kano, T. Ebata, 1977 .

Development of a new cascade reaction for convergent synthesis of pyrazolo[1,5-a]quinoline derivatives under transition-metal-free conditions.

T. Yokomatsu, Jun-ya Kato, Hiroshi Aoyama, 2013, Organic & biomolecular chemistry.

A novel and facile route for the synthesis of medetomidine as the α2-adrenoceptor agonist

H. Aoyama, B. Kaboudin, T. Yokomatsu, 2017, Journal of the Iranian Chemical Society.