M. Nakajima

M. Otagiri, T. Maruyama, Hiroshi Watanabe, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

An extremely mild and stereocontrolled construction of 1,2-trans-β-glycosidic linkages capitalizing on benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors

S. Ikegami, S. Hashimoto, M. Nakajima, 1995 .

Enantioselective conjugate addition of boronic acids to enones catalyzed by O-monoacyltartaric acids.

M. Sugiura, M. Nakajima, Mirai Tokudomi, 2010, Chemical communications.

Enantioselective [2,3]-sigmatropic and [1,2]-Stevens rearrangements via intramolecular formation of allylic oxonium ylides catalyzed by chiral dirhodium(II) carboxylates

S. Kitagaki, S. Hashimoto, M. Anada, 2001 .

Enantioselective Morita–Baylis–Hillman reaction catalyzed by a chiral phosphine oxide

M. Ogasawara, S. Kotani, M. Sugiura, 2013 .

(S)-3,3‘-Dimethyl-2,2‘-biquinoline N,N‘-Dioxide as an Efficient Catalyst for Enantioselective Addition of Allyltrichlorosilanes to Aldehydes

M. Shiro, S. Hashimoto, M. Saito, 1998 .

Enantioselective tandem formation and [2,3]‐sigmatropic rearrangement of cyclic propargylic oxonium ylides catalyzed by dirhodium(II) tetrakis[N‐phthaloyl‐(S)‐tert‐leucinate]

S. Kitagaki, S. Hashimoto, M. Nakajima, 2001 .

Selective Monoacylation of Diols and Asymmetric Desymmetrization of Dialkyl meso-Tartrates Using 2-Pyridyl Esters as Acylating Agents and Metal Carboxylates as Catalysts.

M. Sugiura, M. Nakajima, Y. Hashimoto, 2019, The Journal of organic chemistry.

O-Monoacyltartaric acid catalyzed enantioselective conjugate addition of a boronic acid to dienones: application to the synthesis of optically active cyclopentenones.

M. Sugiura, M. Nakajima, Ryo Kinoshita, 2014, Organic letters.

Enantiocontrol in tandem allylic sulfonium ylide generation and [2,3] sigmatropic rearrangement catalyzed by chiral dirhodium(II) complexes

S. Kitagaki, S. Hashimoto, M. Nakajima, 2001 .

Enantioselective conjugate addition of thiols to enones and enals catalyzed by chiral N-oxide–cadmium complex

S. Hashimoto, M. Saito, M. Nakajima, 2000 .

Enantioselective Conjugate Addition of Thiols to Cyclic Enones and Enals Catalyzed by Chiral N,N′-Dioxide–Cadmium Iodide Complex

S. Hashimoto, M. Saito, M. Nakajima, 2000 .

6.8 Allylations of C-O and C-N Double Bonds and Related Reactions

M. Sugiura, M. Nakajima, 2012 .

Enantioselective 1,2-addition of grignard reagents to aldehydes using chiral diamines

K. Tomioka, K. Koga, M. Nakajima, 1993 .

Enantioselective alkylation at the α-position of cyclic ketones using a chiral lithium amide as a base in the presence of lithium bromide

K. Koga, M. Nakajima, M. Murakata, 1990 .

An Attempt at the Direct Construction of 2-Deoxy-β-glycosidic Linkages Capitalizing on 2-Deoxyglycopyranosyl Diethyl Phosphites as Glycosyl Donors

S. Ikegami, S. Hashimoto, M. Nakajima, 1995 .

An Attempt at the Direct Construction of 2-Deoxy-β-glycosidic Linkages Capitalizing on 2-Deoxyglycopyranosyl Diethyl Phosphites as Glycosyl Donors.

S. Ikegami, S. Hashimoto, M. Nakajima, 1996 .

Asymmetric ring opening of meso-epoxides catalyzed by the chiral phosphine oxide BINAPO

S. Hashimoto, S. Kotani, M. Nakajima, 2005 .

Enantioselective ring opening of meso-epoxides with tetrachlorosilane catalyzed by chiral bipyridine N,N′-dioxide derivatives

S. Hashimoto, M. Saito, M. Nakajima, 2002 .

First asymmetric Abramov-type phosphonylation of aldehydes with trialkyl phosphites catalyzed by chiral Lewis bases

S. Kotani, M. Sugiura, M. Nakajima, 2008 .

A Sterically Congested α‐Cyanoamine as a Cyanating Reagent: Cyanation of Acetals and Orthoesters

S. Kotani, M. Nakajima, Midori Sakamoto, 2015 .

A tertiary amine as a hydride donor: trichlorosilyl triflate-mediated conjugate reduction of unsaturated ketones.

S. Kotani, M. Sugiura, M. Nakajima, 2011, Organic letters.

Asymmetric synthesis of 4H-1,3-oxazines: enantioselective reductive cyclization of N-acylated beta-amino enones with trichlorosilane catalyzed by chiral Lewis bases.

M. Sugiura, M. Nakajima, M. Kumahara, 2009, Chemical communications.

Catalytic asymmetric synthesis of 1,1'-spirobi[indan-3,3'-dione] via a double intramolecular C-H insertion process.

S. Kitagaki, S. Hashimoto, M. Nakajima, 2001, Chemical communications.

O-Monoacyltartaric Acid/(Thio)urea Cooperative Organocatalysis for Enantioselective Conjugate Addition of Boronic Acid.

M. Sugiura, M. Nakajima, T. Yoshimitsu, 2020, Organic letters.

Catalytic Enantioselective Aldol Reactions of Unprotected Carboxylic Acids under Phosphine Oxide Catalysis.

M. Ogasawara, S. Kotani, M. Sugiura, 2018, Angewandte Chemie.

Enantioselective aldol reaction of silyl ketene acetals promoted by a Lewis base-activated Lewis acid catalyst

S. Kotani, M. Sugiura, M. Nakajima, 2009 .

Enantioselective palladium catalyzed allylic alkylation with C2-symmetric chiral diamine ligands

K. Koga, M. Nakajima, H. Kubota, 1993 .

Enantioselective amination of acyclic α-alkylated β-keto esters catalyzed by chiral lithium binaphtholate

S. Kotani, M. Nakajima, Toshifumi Asano, 2016 .

Enantioselective Michael additions of β-keto esters to α,β-unsaturated carbonyl compounds catalyzed by a chiral biquinoline N,N′-dioxide–scandium trifluoromethanesulfonate complex

S. Hashimoto, M. Nakajima, Seiichi Nakamura, 2003 .

Enantioselective alkynylation of carbonyl compounds with trimethoxysilylalkynes catalyzed by lithium binaphtholate

M. Nakajima, Tomohiro Ueda, Kana Tanaka, 2010 .

Sterically congested 'roofed' 2-thiazolines as new chiral ligands for copper(II)-catalyzed asymmetric Diels-Alder reactions

M. Nakajima, T. Kunieda, T. Ishizuka, 2005 .

DMAP-catalyzed cyanation of aldehydes and ketones with ethyl cyanoformate

S. Kotani, M. Sugiura, M. Nakajima, 2010 .

A NEW CATALYTIC SYSTEM FOR AEROBIC OXIDATIVE COUPLING OF 2-NAPHTHOL DERIVATIVES BY THE USE OF CUCL-AMINE COMPLEX : A PRACTICAL SYNTHESIS OF BINAPHTHOL DERIVATIVES

Kenji Koga, K. Koga, Masahiro Noji, 1994 .

Novel use of aryloxyaluminum dichloride in the chiral diamine mediated asymmetric addition reaction of grignard reagents to benzaldehyde

K. Tomioka, K. Koga, M. Nakajima, 1987 .

Enantioselective synthesis of binaphthol derivatives by oxidative coupling of naphthol derivatives catalyzed by chiral diamine-copper complexes

K. Koga, S. Hashimoto, Masahiro Noji, 1999 .

Enantioselective intermolecular 1,3-dipolar cycloaddition via ester-derived carbonyl ylide formation catalyzed by chiral dirhodium(II) carboxylates

S. Kitagaki, S. Hashimoto, M. Anada, 2000 .

A new dirhodium(II) carboxamidate complex as a chiral Lewis acid catalyst for enantioselective hetero-Diels-Alder reactions.

N. Shimada, M. Shiro, S. Kitagaki, 2004, Angewandte Chemie.

Novel enantioselective direct aldol-type reaction promoted by a chiral phosphine oxide as an organocatalyst

S. Kotani, M. Sugiura, M. Nakajima, 2009 .

Asymmetric Direct 1,2-Addition of Aryl Grignard Reagents to Aryl Alkyl Ketones.

M. Nakajima, Kazuki Osakama, 2016, Organic letters.

Chiral lithium binaphtholate for enantioselective amination of acyclic α-alkyl-β-keto esters: Application to the total synthesis of l-carbidopa

S. Kotani, M. Nakajima, Toshifumi Asano, 2017 .

Chiral phosphine oxide BINAPO as a lewis base catalyst for asymmetric allylation and aldol reaction of trichlorosilyl compounds

S. Hashimoto, S. Kotani, M. Nakajima, 2007 .

Chiral phosphine oxide BINAPO as a catalyst for enantioselective allylation of aldehydes with allyltrichlorosilanes

S. Hashimoto, S. Kotani, M. Nakajima, 2005 .

Selective synthesis of optically active allenic and homopropargylic alcohols from propargyl chloride

S. Hashimoto, M. Saito, M. Nakajima, 2002 .

4.10 Enantioselective Aldol Reactions Catalyzed by Chiral Lewis Bases

M. Nakajima, 2012 .

Trichlorosilyl triflate for enantioselective direct-type aldol reaction with chiral phosphine oxide

S. Kotani, M. Sugiura, M. Nakajima, 2011 .

Enantioselective chlorinative aldol reaction of α-substituted acroleins catalyzed by chiral phosphine oxides

S. Kotani, M. Sugiura, M. Nakajima, 2017 .

Enantioselective reductive aldol reaction using tertiary amine as hydride donor

S. Kotani, M. Sugiura, M. Nakajima, 2012 .

One-pot enantioselective synthesis of optically active homoallylic alcohols from allyl halides.

S. Hashimoto, M. Saito, M. Nakajima, 2000, Chemical & pharmaceutical bulletin.

Enantioselective double aldol reaction catalyzed by chiral phosphine oxide.

S. Kotani, M. Sugiura, M. Nakajima, 2011, Chemistry.

Synthesis of aryl group-modified DIOP dioxides (Ar-DIOPOs) and their application as modular Lewis base catalysts.

S. Kotani, M. Sugiura, M. Nakajima, 2012, Organic & biomolecular chemistry.

Enantioface differentiation in cis dihydroxylation of carbon-carbon double bonds by osmium tetroxide using a chiral diamine with D2 symmetry

K. Tomioka, K. Koga, M. Nakajima, 1987 .

Regioselective enolization of optically active 3-keto steroids using chiral lithium amides

K. Koga, M. Nakajima, M. Sobukawa, 1990 .

Highly enantioselective dihydroxylation of olefins by osmium tetroxide with chiral diamines

K. Tomioka, M. Nakajima, Koga Kenji, 1993 .

Enantioselective Conjugate Addition of Thiols to Cyclic Enones and Enals Catalyzed by Chiral N,N′‐Dioxide—Cadmium Iodide Complex.

S. Hashimoto, M. Saito, M. Nakajima, 2001 .

Enantioselective Michael addition of beta-keto esters to methyl vinyl ketone employing a chiral N,N'-dioxide-scandium trifluoromethanesulfonate complex as a catalyst.

S. Hashimoto, M. Nakajima, Y. Yamaguchi, 2001, Chemical communications.

A novel axially dissymmetric chiral ligand based on amine N-oxide: (R)- and (S)-3,3'-dimethyl-2,2'-biquinoline N,N'-dioxide

M. Shiro, S. Hashimoto, M. Nakajima, 1997 .

Synthesis and evaluation of novel dirhodium(II) carboxylate catalysts with atropisomeric biaryl backbone

M. Shiro, S. Kitagaki, S. Hashimoto, 2003 .

Synthesis of conjugated multiunsaturated thioesters via one-pot TiCl4-promoted aldol condensation

M. Sugiura, M. Nakajima, Y. Ashikari, 2020 .

One-Pot Synthesis of β,β-Disubstituted α,β-Unsaturated Carbonyl Compounds.

M. Sugiura, M. Nakajima, Y. Ashikari, 2015, The Journal of organic chemistry.

Bipyridine N,N′-Dioxide: A Felicitous Ligand for Methyltrioxorhenium-Catalyzed Epoxidation of Olefins with Hydrogen Peroxide

H. Iwamoto, S. Hashimoto, M. Nakajima, 1998 .

Development of chiral dinitrones as modular Lewis base catalysts: asymmetric allylation of aldehydes with allyltrichlorosilanes

S. Kotani, M. Sugiura, M. Nakajima, 2010 .

Chiral base-catalyzed aldol reaction of trimethoxysilyl enol ethers: effect of water as an additive on stereoselectivities

S. Hashimoto, M. Nakajima, T. Ishizuka, 2006 .

A chiral "roofed" cis-diamine-Ru(II) complex: An efficient catalyst for asymmetric transfer hydrogenation of ketimines

M. Nakajima, T. Kunieda, T. Ishizuka, 2009 .

Lithium binaphtholate-catalyzed asymmetric addition of lithium acetylides to carbonyl compounds.

S. Kotani, M. Nakajima, Kana Tanaka, 2014, The Journal of organic chemistry.

Lithium acetylides as alkynylating reagents for the enantioselective alkynylation of ketones catalyzed by lithium binaphtholate.

S. Kotani, M. Nakajima, Kana Tanaka, 2011, Chemical communications.

Enantioselective alkynylation of ketones with trimethoxysilylalkynes using lithium binaphtholate as a catalyst

M. Nakajima, Tomohiro Ueda, Kana Tanaka, 2010 .

Stereoselective Synthesis of 2-Fluoro-1,3-Diols via Lithium Binaphtholate-Catalyzed Aldol-Tishchenko Reaction.

S. Kotani, M. Nakajima, Toshifumi Asano, 2019, Organic letters.

Construction of quaternary carbon centers by a base-catalyzed enantioselective aldol reaction and related reactions of trimethoxysilyl enol ethers

S. Kotani, M. Nakajima, T. Kaneko, 2012 .

Enantioselective construction of quaternary asymmetric carbon centers using an aldol reaction of trimethoxysilyl enol ethers catalyzed by lithium binaphtholate

M. Nakajima, T. Ichibakase, Yuya Orito, 2008 .

Enantioselective aldol reaction of trimethoxysilyl enol ether catalyzed by lithium binaphtholate.

S. Hashimoto, M. Nakajima, T. Ishizuka, 2004, Organic letters.

Aerobic Oxidative Coupling of 2-Naphthol Derivatives Catalyzed by a Copper-Amine Complex without Solvent

K. Koga, S. Hashimoto, Masahiro Noji, 1998 .

Catalytic asymmetric synthesis of binaphthol derivatives by aerobic oxidative coupling of 3-hydroxy-2-naphthoates with chiral diamine-copper complex

Shunichi Hashimoto, S. Hashimoto, Makoto Nakajima, 1995 .

Chiral Lithium Binaphtholate for Enantioselective Michael Addition of Acyclic α‐Alkyl‐β‐Keto Esters to Vinyl Ketones

S. Kotani, M. Nakajima, M. Moritani, 2015 .

Trichlorosilyl triflate-mediated enantioselective directed cross-aldol reaction between ketones using a chiral phosphine oxide as an organocatalyst.

S. Kotani, M. Sugiura, M. Nakajima, 2012, Chemical communications.

Enantioselective Aldol Reactions of Trichlorosilyl Enol Ethers Catalyzed by the Chiral Phosphine Oxide BINAPO

S. Hashimoto, S. Kotani, M. Nakajima, 2006 .

An extremely mild and stereocontrolled construction of 1,2-cis-α-glycosidic linkages via benzyl-protected glycopyranosyl diethyl phosphites

Hiroko Tanaka, S. Hashimoto, M. Nakajima, 1999 .

Aromatic-Turmerone Analogs Protect Dopaminergic Neurons in Midbrain Slice Cultures through Their Neuroprotective Activities

Y. Kurauchi, A. Hisatsune, T. Seki, 2021, Cells.

Catalytic Enantioselective Tandem Carbonyl Ylide Formation/1,3-Dipolar Cycloaddition Reactions of α-Diazo Ketones with Aromatic Aldehydes using Dirhodium(II) Tetrakis[N-benzene-fused-phthaloyl-(S)-valinate]

N. Shimada, Takumi Abe, S. Hashimoto, 2007 .

Novel 3,4-diarylpyrrolidine-based chiral ligands for the asymmetric reaction of arylmagnesium bromides with aldehydes.

K. Tomioka, K. Koga, M. Nakajima, 1987 .

Enantioselective Evans-Tishchenko Reduction of β-Hydroxyketone Catalyzed by Lithium Binaphtholate

M. Nakajima, T. Ichibakase, Masatoshi Nakatsu, 2011, Molecules.

Short-step asymmetric syntheses of anthracycline antibiotics via enantioselective dihydroxylation by osmium tetroxide with a chiral diamine

K. Tomioka, K. Koga, M. Nakajima, 1993 .

Stereoselective synthesis of multiple stereocenters by using a double aldol reaction.

S. Kotani, M. Sugiura, M. Nakajima, 2013, Angewandte Chemie.

Enantioselective deprotonation of the meso-forms of 2,6- and 3,5-dimethylcyclohexanones

R. Shirai, K. Koga, H. Kawasaki, 1990 .

Kinetic resolution of racemic 2-substituted cyclohexanones by enantioselective deprotonation

K. Koga, H. Kawasaki, M. Nakajima, 1989 .

Chiral lithium 2-aminoalkoxides as reagents for enantioselective Michael reaction

K. Koga, S. Aoki, Takuya Kumamoto, 1994 .

Dramatic Enantioselectivity Reversal in the Propargylation of Aldehyde with Alkynyllithium Catalyzed by Dilithium Binaphtholate Derivatives

M. Nakajima, Midori Sakamoto, Kazuki Osakama, 2018 .

Design and synthesis of novel chiral pyrrolidine-based diamines with C2-symmetry

K. Tomioka, K. Koga, M. Nakajima, 1993 .

Enantioselective aldol reactions catalyzed by chiral phosphine oxides.

S. Kotani, M. Sugiura, M. Nakajima, 2013, Chemical record.

Highly Selective Glycosidation Reactions Capitalizing on Phosphorus-containing Leaving Groups

S. Ikegami, S. Hashimoto, M. Nakajima, 1995 .

AN EXTREMELY MILD AND GENERAL METHOD FOR THE CONSTRUCTION OF 1, 2-TRANS-β-GLYCOSIDIC LINKAGES VIA GLYCOPYRANOSYL DIETHYL PHOSPHITES WITH PARTICIPATING GROUPS AT C-2

S. Ikegami, S. Hashimoto, M. Nakajima, 1995 .

Studies directed toward the total synthesis of pinnatoxin A: synthesis of the 6,5,6-dispiroketal (BCD ring) system by double hemiketal formation/hetero-Michael addition strategy

S. Hashimoto, M. Nakajima, Seiichi Nakamura, 2002 .

Dramatic enantioselectivity change in dihydroxylation of olefins with chiral amine-osmium tetroxide complex

K. Tomioka, K. Koga, M. Nakajima, 1990 .

A short asymmetric synthesis of anthracycline antibiotics

K. Tomioka, K. Koga, M. Nakajima, 1989 .

Mechanistic aspects of asymmetric cis-dihydroxylation of olefins with osmium tetroxide employing a C2-symmetric chiral diamine

K. Tomioka, K. Koga, Y. Iitaka, 1988 .

Reinvestigation on the optical purities of optically active trimethylsilyl enol ethers of 4-substituted cyclohexanones

K. Tomioka, K. Koga, K. Aoki, 1993 .

Facile synthesis of chiral 1,2-chlorohydrins via the ring-opening of meso-epoxides catalyzed by chiral phosphine oxides

S. Kotani, M. Sugiura, M. Nakajima, 2013 .

6.21 C-X Bond Formation: Organocatalytic Enantioselective Halogenation of meso Epoxides

S. Kotani, M. Nakajima, 2012 .

Concise Asymmetric Construction of C2 -symmetric 1,9-Diarylnonanoids Using a Hypervalent Silicon Complex: Total Synthesis of (-)-Ericanone.

Haoxiang Hu, M. Ogasawara, S. Kotani, 2016, Chemistry, an Asian journal.

Diastereoselective synthesis of 1,3-diamines by a domino reaction of imines, enamines, and trichlorosilane

S. Kotani, M. Sugiura, M. Nakajima, 2014 .

Facile Synthesis of Chiral 1,2‐Chlorohydrins via the Ring‐Opening of meso‐Epoxides Catalyzed by Chiral Phosphine Oxides.

S. Kotani, M. Sugiura, M. Nakajima, 2013 .

A stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A.

S. Hashimoto, M. Nakajima, T. Sugimoto, 2001, Organic letters.

p-Cresyl sulfate, a uremic toxin, causes vascular endothelial and smooth muscle cell damages by inducing oxidative stress

Masafumi Fukagawa, Toru Maruyama, Kazutaka Matsushita, 2014, Pharmacology research & perspectives.

Enantiocontrol in Tandem Allylic Sulfonium Ylide Generation and [2,3] Sigmatropic Rearrangement Catalyzed by Chiral Dirhodium(II) Complexes.

S. Kitagaki, S. Hashimoto, M. Nakajima, 2001 .

Stereoselective reactions. XIX. Asymmetric dihydroxylation of olefins by employing osmium tetroxide-chiral amine complexes

K. Tomioka, K. Koga, M. Nakajima, 1990 .

Imino ene-type reaction of enamines with N-sulfonylimines and application to diastereoselective synthesis of N-sulfonyl-1,3-diamines

S. Kotani, M. Sugiura, M. Nakajima, 2014 .

Isolation, Synthesis, and Structure-Activity Relationship Study on Daphnane and Tigliane Diterpenes as HIV Latency-Reversing Agents.

Teppei Kawahara, Teruya Nakamura, N. Kishimoto, 2022, Journal of medicinal chemistry.

Arteperoxides A-C, tris-normonoterpene-sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity.

S. Tsukamoto, H. Kato, S. Kotani, 2022, Phytochemistry.

Oxidative Intramolecular Phenolic Coupling Reaction Induced by a Hypervalent Iodine(III) Reagent: Leading to Galanthamine-Type Amaryllidaceae Alkaloids.

Y. Kita, M. Arisawa, M. Nakajima, 1999 .

Enantioselective Double Aldol Reactions Involving the Sequential Activation of Silicon Tetrachloride by Chiral Phosphine Oxides

S. Kotani, M. Sugiura, M. Nakajima, 2014, Synlett.

Enantioselective and Chemoselective Phosphine oxide-catalyzed Aldol Reaction of N-Unprotected Cyclic Carboxyimides.

S. Kotani, M. Nakajima, Yusaku Yoshiwara, 2022, Chemistry.

Phosphine oxide-catalyzed enantioselective intramolecular aldol reaction via regioselective enolization of unsymmetrical diketones with tetrachlorosilane.

M. Ogasawara, S. Kotani, M. Sugiura, 2014, Organic letters.

Chiral Phosphine Oxide BINAPO as a Lewis Base Catalyst for Asymmetric Allylation and Aldol Reaction of Trichlorosilyl Compounds.

S. Hashimoto, S. Kotani, M. Nakajima, 2007 .

p-Cresyl sulfate causes renal tubular cell damage by inducing oxidative stress by activation of NADPH oxidase.

M. Otagiri, T. Maruyama, Hiroshi Watanabe, 2013, Kidney international.

Organic anion transporters play an important role in the uptake of p-cresyl sulfate, a uremic toxin, in the kidney.

M. Otagiri, T. Maruyama, Hiroshi Watanabe, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Enantioselective aldol reactions of trichlorosilyl enol ethers catalyzed by chiral N,N′-dioxides and monodentate N-oxides

M. Saito, M. Nakajima, S. Hashimoto*, 2004 .