Y. Ukaji

发表

Total Syntheses of Sterically Locked Phycocyanobilin Derivatives Bearing a 15Z-anti or a 15E-anti CD-Ring Component

H. Kinoshita, Kaori Nishiyama, A. Kamiya, 2010 .

Discovery of Selective Transforming Growth Factor β Type II Receptor Inhibitors as Antifibrosis Agents.

Makoto Shiozaki, M. Yokota, Y. Ukaji, 2021, ACS medicinal chemistry letters.

5.20 Addition Reaction: Cycloaddition Involving Oxidation (N=N, N=O; No C–C Bond Formed)

Y. Ukaji, 2012 .

Assembly of Synthetic Locked Phycocyanobilin Derivatives with Phytochrome in Vitro and in Vivo in Ceratodon purpureus and Arabidopsis[C][W]

Rui Yang, T. Lamparter, Kaori Nishiyama, 2012, Plant Cell.

Silver(I) Oxide-promoted Chemoselective Cross-coupling Reaction of (Diborylmethyl)trimethylsilane

K. Endo, Y. Ukaji, Fumiya Kurosawa, 2013 .

N-heterocyclic carbene catalyzed oxidative coupling of aldehydes with carbodiimides under aerobic conditions: efficient synthesis of N-acylureas.

T. Soeta, S. Fujinami, Y. Ukaji, 2013, Organic letters.

One‐Shot Radical Cross Coupling Between Benzyl Alcohols and Alkenyl Halides Using Ni/Ti/Mn System

Y. Ukaji, T. Suga, Yuuki Takahashi, 2020 .

Nickel-Catalyzed Cross-Electrophile Coupling between Benzyl Alcohols and Aryl Halides Assisted by Titanium Co-reductant.

Y. Ukaji, T. Suga, 2018, Organic letters.

One-pot stereoselective synthesis of 2-acylaziridines and 2-acylpyrrolidines from N-(propargylic)hydroxylamines.

T. Soeta, S. Fujinami, Y. Ukaji, 2013, Chemistry, an Asian journal.

The Lewis acid-catalyzed [3+1+1] cycloaddition of azomethine ylides with isocyanides

T. Soeta, S. Fujinami, Y. Ukaji, 2014 .

Stereoselective synthesis of (2Z,4E)-2,4-pentadien-1-ols via sequential 1,4-elimination reaction and [1,2]-Wittig rearrangement starting from (E)-4-alkoxy-2-butenyl benzoates.

T. Nakano, T. Soeta, K. Endo, 2013, The Journal of organic chemistry.

N-Heterocyclic Carbene-Catalyzed Chemoselective Monoacylation of 1,n-Linear Diols.

T. Ida, T. Soeta, Y. Ukaji, 2021, Organic letters.

Low-Valent Titanium-Mediated Radical Conjugate Addition Using Benzyl Alcohols as Benzyl Radical Sources.

Y. Ukaji, T. Suga, Sho Shimazu, 2018, Organic letters.

Cyclopropenes for the Stepwise Synthesis of 1,2,4,5-Tetraarylbenzenes via 1,4-Cyclohexadienes

K. Endo, Y. Ukaji, S. Kishida, 2022, The Journal of organic chemistry.

Selective Transformation of N-(Propargylic)hydroxylamines into 4-Isoxazolines and Acylaziridines Promoted by Metal Salts

Y. Ukaji, K. Inomata, Norihiro Wada, 2011 .

Syn-effect in the isomerization of (E)-α-fluorovinylic sulfones to the corresponding allylic sulfones under basic conditions

Y. Ohta, Y. Ukaji, K. Inomata, 2002 .

Synthesis of Sterically Fixed Phytochrome Chromophore Derivatives Bearing a 15 E- Fixed or 15 E- Anti- Fixed CD-Ring Component.

Y. Sakata, Toshiharu Kobayashi, T. Soeta, 2018, The Journal of organic chemistry.

Reversal of Diastereofacial Selectivity in the Addition Reaction of Organometallics to Chiral Imines

Y. Ukaji, T. Fujisawa, Takashi Sumi, 1991 .

Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides Generated in situ by Direct Oxidation of Aldoximes

M. Tsuji, Y. Ukaji, K. Inomata, 2002 .

Enantioselective Synthesis of 2-Isoxazolines via Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxide to Achiral Allyl Alcohol

Y. Ukaji, K. Inomata, K. Sada, 1993 .

Palladium-catalyzed C–H Alkenylation of C-Aryl Nitrones

T. Soeta, Y. Ukaji, T. Suga, 2017 .

Chiral NHC ligands bearing a pyridine moiety in copper-catalyzed addition of diethylzinc to nitroalkenes

T. Soeta, Y. Ukaji, Y. Hatanaka, 2018, Tetrahedron.

Chiral NHC Ligands Bearing a Pyridine Moiety in Copper-Catalyzed 1,2-Addition of Dialkylzinc Reagents to β-Aryl-α,β-unsaturated N-Tosylaldimines.

T. Soeta, Y. Ukaji, Tomohiro Ishizaka, 2016, The Journal of organic chemistry.

Chiral N-heterocyclic carbene ligands bearing a pyridine moiety for the copper-catalyzed alkylation of N-sulfonylimines with dialkylzinc reagents.

T. Soeta, Y. Ukaji, Tomohiro Ishizaka, 2014, Chemistry.

An asymmetric intramolecular Stetter reaction catalyzed by a chiral triazolium precatalyst bearing a pyridine moiety

T. Soeta, Y. Ukaji, Yuhta Tabatake, 2012 .

Asymmetric cross-benzoin condensation promoted by a chiral triazolium precatalyst bearing a pyridine moiety

T. Soeta, Y. Ukaji, Y. Hatanaka, 2012 .

Carboxylic acid free novel isocyanide-based reactions.

T. Soeta, Y. Ukaji, 2014, Chemical record.

Chlorosilane-promoted addition reaction of isocyanides to 3,4-dihydroisoquinoline N-oxides.

T. Soeta, S. Fujinami, Y. Ukaji, 2012, The Journal of organic chemistry.

Development of a One-Pot Synthetic Method for Multifunctional Oxazole Derivatives Using Isocyanide Dichloride.

Y. Sakata, T. Soeta, Y. Ukaji, 2017, The Journal of organic chemistry.

Development of New Methods for The Construction of Heterocycles Based on Cycloaddition Reaction of 1,3‐Dipoles

T. Soeta, Y. Ukaji, 2014 .

[5+1] cycloaddition of C,N-cyclic N'-acyl azomethine imines with isocyanides.

T. Soeta, Y. Ukaji, Kaname Tamura, 2012, Organic letters.

Borinic acid catalyzed α-addition to isocyanide with aldehyde and water

T. Soeta, Y. Ukaji, K. Inomata, 2011 .

Stereoselective Preparation of Acyclic syn-β-Amino Alcohols from β-Hydroxy Ketones via the Corresponding O-Benzyl Oximes

Y. Ukaji, K. Narasaka, Shigeru Yamazaki, 1986 .

A FACILE METHOD FOR THE STEREOSELECTIVE PREPARATION OF ACYCLIC syn-1,3-AMINO ALCOHOLS FROM β-HYDROXY KETONES

Y. Ukaji, K. Narasaka, Shigeru Yamazaki, 1984 .

A NEW APPROACH TO THE SYNTHESIS OF A LYTHRACEAE ALKALOID, LASUBINE II

Y. Ukaji, K. Narasaka, Shigeru Yamazaki, 1985 .

A three-component reaction of C,N-cyclic N'-acyl azomethine imines, isocyanides, and azide compounds: effective synthesis of 1,5-disubstituted tetrazoles with tetrahydroisoquinoline skeletons.

T. Soeta, S. Fujinami, Y. Ukaji, 2013, Organic & biomolecular chemistry.

Diastereoface-discrimination reaction of lithium or titanium ester enolates with a chiral imine leading to stereodivergent synthesis of β-lactams

M. Shimizu, Y. Ukaji, T. Fujisawa, 1992 .

Diastereofacial Control in the Reaction of Chiral α-Amino Ketones with Several Organometallics

T. Sato, Y. Ukaji, T. Fujisawa, 1988 .

Asymmetric addition of phenylzinc reagents to C-alkynyl nitrones. Enantiomeric enhancement by a product-like additive

Y. Ukaji, K. Inomata, Weilin Wei, 2008 .

Catalytic Asymmetric Addition of Alkynylzinc Reagents to Nitrones

Masato Kobayashi, S. Fujinami, Y. Ukaji, 2007 .

Asymmetric Addition of Alkynylzinc Reagents to Nitrones Utilizing Tartaric Acid Ester as a Chiral Auxiliary

Masato Kobayashi, Y. Ukaji, K. Inomata, 2006 .

A stereodivergent construction of β-lactam skeletons via condensation of ester enolates and a chiral imine

M. Shimizu, Y. Ukaji, T. Fujisawa, 1991 .

[4+1] Cycloaddition of N-acylimine derivatives with isocyanides: efficient synthesis of 5-aminooxazoles and 5-aminothiazoles

T. Soeta, Y. Ukaji, Kaname Tamura, 2014 .

Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines to Homoallylic Alcohols

S. Fujinami, Y. Ukaji, K. Inomata, 2010 .

Magnesium-tartramide complex mediated asymmetric Strecker-type reaction of nitrones using cyanohydrin.

T. Soeta, K. Endo, S. Fujinami, 2013, Organic letters.

Strecker-Type Reaction of Nitrones Using Cyanohydrin

T. Soeta, Y. Ukaji, K. Inomata, 2012 .

"Syn-Effect" in Nucleophilic Addition of Amines to 1,3-Dienylsulfone

Y. Ukaji, K. Inomata, S. Guha, 2006 .

Desymmetrization of meso-methylenecyclopropanes by a palladium-catalyzed asymmetric ring-opening bis(alkoxycarbonylation) reaction

Y. Yonezawa, S. Fujinami, Y. Ukaji, 2014 .

Palladium-Catalyzed Carbonylation of Homoallylic Amine Derivatives in the Presence of a Copper Co-catalyst

Y. Ukaji, K. Inomata, T. Mizutani, 2003 .

Regulation of Diastereofacial Selection in the Allylation Reaction of N-Acyliminium Ion Utilizing Lewis Acids

M. Shimizu, Y. Ukaji, T. Fujisawa, 1993 .

Asymmetric Bis(alkoxycarbonylation) Reaction of Homoallylic Alcohols Catalyzed by Palladium in the Presence of Cu(I) Triflate Using the Chiral Bioxazoline Ligand

Y. Ukaji, K. Inomata, Masanori Miyamoto, 1996 .

One-Carbon Homologation of Pyrrole Carboxaldehyde via Wittig Reaction and Mild Hydrolysis of Vinyl Ether – toward the Synthesis of a Sterically Locked Phytochrome Chromophore

T. Soeta, Y. Ukaji, R. Sakata, 2015 .

A one-pot O-phosphinative Passerini/Pudovik reaction: efficient synthesis of highly functionalized α-(phosphinyloxy)amide derivatives.

T. Soeta, Y. Ukaji, Syunsuke Matsuzaki, 2014, Chemistry.

A one-pot O-sulfinative Passerini/oxidation reaction: synthesis of α-(sulfonyloxy)amide derivatives.

T. Soeta, Y. Ukaji, Syunsuke Matsuzaki, 2015, The Journal of organic chemistry.

Direct preparation of substituted olefins from epoxides utilizing lithium tetraalkylcerate

Y. Ukaji, T. Fujisawa, 1988 .

Catalytic asymmetric dialkynylation reaction of α-dinitrone by utilizing tartaric acid ester as a chiral auxiliary

S. Fujinami, Y. Ukaji, K. Inomata, 2008 .

Selective 1,4-Chiral Induction in the Reaction of Enolates Generated from t-Butyl δ-Hydroxy Carboxylates

Y. Ukaji, K. Narasaka, Kazutoshi Watanabe, 1987 .

Homologation Reaction of γ-Silicon Substituted Allylic Alcohols Using Organoaluminium Reagents and Diiodomethane

Y. Ukaji, K. Inomata, 1992 .

Enantioselective Construction of Cyclopropane Rings via Asymmetric Simmons-Smith Reaction of Allylic Alcohols

Y. Ukaji, T. Fujisawa, M. Nishimura, 1992 .

A stereocontrolled method for the synthesis of each of the four diastereomers of 34-dialkyl-substituted β-lactams using different metal ester enolates and a chiral imine

M. Shimizu, Y. Ukaji, T. Fujisawa, 1993 .

Highly Stereodivergent Approach to Both Enantiomers of 4-Substituted β-Lactams via Diastereofacially Controlled Addition of Enolates of t-Butyl Acetate to a Chiral Imine

J. Tanizaki, M. Shimizu, Y. Ukaji, 1992 .

Either diastereofacial differentiation in the reaction of chiral thiomethylketones with appropriate organometallics

Y. Ukaji, T. Fujisawa, I. Takemura, 1990 .

Stereodivergent synthesis of optically active tertiary alcohols via addition reaction of chiral 2-acyl oxazolidine with organometallics

Y. Ukaji, K. Yamamoto, T. Fujisawa, 1991 .

Diastereofacial Discrimination in the Reaction of Chiral Alkoxymethyl Oxime Ethers with Allyl Metallic Reagents

Y. Ukaji, T. Fujisawa, T. Watai, 1991 .

Stereocontrolled Addition Reaction of Organometallics to Chiral α-Keto Amides

T. Sato, Y. Ukaji, T. Fujisawa, 1990 .

Catalytic Asymmetric 1,3-Dipolar Cycloaddition of a Nitrone Bearing a Bulky Amide Moiety to γ-Substituted Allylic Alcohols

S. Fujinami, Y. Ukaji, K. Inomata, 2002 .

A Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Allyl Alcohol

Y. Ukaji, K. Inomata, Xia Ding, 2001 .

Enantio- and Diastereoselective Synthesis of Isoxazolidines by Asymmetric 1, 3-Dipolar Cycloaddition of Nitrones

Y. Ukaji, K. Inomata, K. Sada, 1997 .

Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol

S. Fujinami, Y. Ukaji, K. Inomata, 2008 .

Formal Total Synthesis of Manzacidin C Based on Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines.

T. Soeta, Y. Ukaji, Y. Hayashi, 2017, The Journal of organic chemistry.

Desymmetrization of 1,4-pentadien-3-ol by the asymmetric 1,3-dipolar cycloaddition of azomethine imines.

T. Soeta, S. Fujinami, Y. Ukaji, 2014, Chemistry.

CATALYTIC ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION OF AZOMETHINE IMINES TO ALLYL ALCOHOL UTILIZING TARTARIC ACID ESTER AS A CHIRAL AUXILIARY

Y. Ukaji, Katsuyoshi Tanaka, Tomomitsu Kato, 2010 .

1,3-Asymmetric Induction in the Reaction of Organometallics to β-Hydroxy Ketones and β-Silyloxy Ketones

H. Kanda, Y. Ukaji, K. Yamamoto, 1990 .

HIGHLY STEREOSELECTIVE ALKYLATION REACTION OF ESTER ENOLATES GENERATED FROM δ-HYDROXY CARBOXYLIC ACID ESTERS

Y. Ukaji, K. Narasaka, 1986 .

Ring enlargement reaction of C,N-cyclic-N'-acyl azomethine imines with sulfonium ylide: an efficient synthesis of 3-benzazepine derivatives.

T. Soeta, S. Fujinami, Y. Ukaji, 2014, Organic letters.

(Z)-Selective Enol Triflation of α-Alkoxyacetoaldehydes: Application to Synthesis of (Z)-Allylic Alcohols via Cross-Coupling Reaction and [1,2]-Wittig Rearrangement.

T. Nakano, T. Soeta, K. Endo, 2015, The Journal of organic chemistry.

One pot synthesis of optically active 4-isoxazolines by asymmetric addition of alkynylzinc reagents to nitrones followed by cyclization

Masato Kobayashi, Y. Ukaji, K. Inomata, 2009 .

Silver-Catalyzed Allylation of Ketones and Intramolecular Cyclization through Carbene Intermediates from Cyclopropenes Under Ambient Conditions.

T. Nakano, K. Endo, Y. Ukaji, 2016, Chemistry, an Asian journal.

Catalytic tandem C-C bond formation/cleavage of cyclopropene for allylzincation of aldehydes or aldimine using organozinc reagents.

T. Nakano, K. Endo, Y. Ukaji, 2014, Organic letters.

Stereoselective syntheses of carbon homologated vinylsilanes and desilylated olefins from α,β-epoxy silanes using organolithium and organolanthanoid reagents

Y. Ukaji, T. Fujisawa, A. Yoshida, 1990 .

A facile method for the cleavage of acetals by the combined use of samarium trichloride and chlorotrimethylsilane

Y. Ukaji, T. Fujisawa, Naosuke Koumoto, 1989 .

Diastereofacial Control in the Reaction of (R)-α-(p-Tolylsulfinyl)acetophenones with Several Organometallics

Y. Ukaji, T. Fujisawa, Atsushi Fujimura, 1988 .

Palladium-catalyzed Intermolecular Alkoxy-alkoxycarbonylation of Vinylphenols in the Presence of Copper Salt: Unexpected Cooperative Effect of Tin Salt

N. Phan, T. Soeta, Y. Ukaji, 2016 .

Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary

S. Fujinami, Y. Ukaji, K. Inomata, 2006 .

DIRECT OXIDATION OF 4-METHYLPYRROLE-2-CARBOXYLATES WITH DDQ IN THE PRESENCE OF A GLYCOL (Dedicated to Professor Dr. Ei-ichi Negishi on the occasion of his 77th birthday)

T. Soeta, Y. Ukaji, K. Inomata, 2012 .

3.6 Acetogenin (Polypriopionate) Derived Auxiliaries: Tartaric Acid

T. Soeta, Y. Ukaji, 2012 .

Synthesis of Silicon Substituted Cyclopropylmethyl Alcohols in Optically Active Form via Asymmetric Simmons-Smith Reaction of γ-Silicon Substituted Allylic Alcohols

Y. Ukaji, K. Inomata, K. Sada, 1993 .

Asymmetric Benzoin Condensation Promoted by Chiral Triazolium Precatalyst Bearing a Pyridine Moiety.

T. Soeta, Y. Ukaji, K. Inomata, 2012 .

Diastereoface‐Discrimination Reaction of Lithium or Titanium Ester Enolates with a Chiral Imine Leading to Stereodivergent Synthesis of . beta.‐Lactams.

M. Shimizu, Y. Ukaji, T. Fujisawa, 1992 .

Diastereofacial controlled addition reaction of alkoxymethylketones modified by (2R,4R)-2,4-pentanediol with organometallics.

Y. Ukaji, T. Fujisawa, T. Watai, 1989 .

Stereoselective One-pot 1,4-Elimination and the [1,2]-Wittig Rearrangement of (E)-δ-(Arylmethoxy or 3-Silyl-2-propynyloxy)-substituted Allylic Sulfones

Y. Ukaji, K. Inomata, Isao Ishimaru, 2011 .

Recent progress in a chiral multinucleating system utilizing tartaric acid esters.

Y. Ukaji, K. Inomata, 2010, Chemical record.

Catalytic Asymmetric Addition of Alkynylzinc Reagents to Nitrones.

Masato Kobayashi, S. Fujinami, Y. Ukaji, 2007 .

Synthesis of 3,6-Dihydro-2H-1,2-oxazines via Dimethylsulfoxonium Methylide Addition to α,β-Unsaturated Nitrones.

T. Soeta, Y. Ukaji, T. Suga, 2020, The Journal of organic chemistry.

Control of Enantiofacial Differentiation in the Addition Reaction of Organometallics to a Nitrone in the Presence of an External Chiral Auxiliary

Alauddin Ahmed, Y. Ukaji, K. Inomata, 1993 .

Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to γ-Substituted Allylic Alcohols

S. Fujinami, Y. Ukaji, K. Inomata, 1998 .

''Syn Effect'' in Nucleophilic Addition of Amines to 1,3-Dienyl Sulfone and Ethyl (E)-2,4-Pentadienoate

Y. Ukaji, K. Inomata, S. Guha, 2008 .

Asymmetric Addition of Reformatsky-Type Reagent to Imines Utilizing Diisopropyl Tartrate as a Chiral Auxiliary

Y. Ukaji, K. Inomata, Shoichi Takenaka, 2001 .

Asymmetric addition of a Reformatsky-type reagent to 3,4-dihydroisoquinoline N-oxides

Y. Ukaji, K. Inomata, Yayoi Yoshida, 2000 .

Catalytic Asymmetric Addition Reaction of Dialkylzinc to Nitrone Utilizing Tartaric Acid Ester as a Chiral Auxiliary.

Alauddin Ahmed, Y. Ukaji, K. Inomata, 1997 .

Asymmetric addition reaction of organozinc reagents to nitrones using a catalytic amount of external chiral auxiliary

Y. Ukaji, K. Inomata, Y. Kenmoku, 1996 .

Total Syntheses of Sterically Locked Phycocyanobilin Derivatives Bearing a 15Z‐anti or a 15E‐anti CD‐Ring Component.

H. Kinoshita, Kaori Nishiyama, A. Kamiya, 2010 .

Highly (E)-Selective Trisubstituted Alkene Synthesis by Low-Valent Titanium-Mediated Homolytic Cleavage of Alcohol C-O Bond.

Y. Ukaji, T. Suga, Mizuki Sakata, 2022, The Journal of organic chemistry.

Stereoselective conjugate addition of halide anion to acetylenic carbonyl compounds promoted by lanthanoid reagents

Y. Ukaji, T. Fujisawa, A. Tanaka, 1989 .

“Syn-Effect” in the Conversion of (E)-α,β-Unsaturated Esters into the Corresponding β,γ-Unsaturated Esters and Aldehydes into Silyl Enol Ethers

A. Shibayama, Y. Ukaji, K. Inomata, 2004 .

Diastereofacial Control in the Reaction of Chiral α-Amino Ketones with Several Organometallics.

T. Sato, Y. Ukaji, T. Fujisawa, 1988 .

Stereoselective Alkylation of Lithium Enolates Generated from t-Butyl Esters of 4-Alkyl-Substituted 5-Hydroxypentanoic Acids

Y. Ukaji, K. Narasaka, 1988 .

Stereoselective Alkylation of Lithium Enolates Generated from t-Butyl Esters of 4-Alkyl-Substituted 5-Hydroxypentanoic Acids.

Y. Ukaji, K. Narasaka, 1988 .

Palladium-Catalyzed Elimination Reaction of Acyclic (E)-Allylic Acetates : The Stereochemistry Elucidated by "Syn-Effect"

H. Takenaka, Y. Ukaji, K. Inomata, 2005 .

Development of Selective Synthetic Processes Leading to Fine Chemicals

Y. Ukaji, T. Fujisawa, 1989 .

Development of Selective Synthetic Processes Leading to Fine Chemicals. Diastereofacial Control in the Nucleophilic Addition to Carbonyl Compounds

Y. Ukaji, T. Fujisawa, 1989 .

Preparation of novel N-sulfonylated (S,S)-2,3-diaminosuccinate-type chiral auxiliaries and application to an asymmetric 1,3-dipolar cycloaddition reaction of nitrile oxides to allyl alcohol

Y. Ukaji, K. Inomata, Masakazu Serizawa, 2006 .

Preparation of Novel N-Sulfonylated (S,S)-2,3-Diaminosuccinate-Type Chiral Auxiliaries and Application to an Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxides to Allyl Alcohol.

Y. Ukaji, K. Inomata, Masakazu Serizawa, 2007 .

Enantioselective Diels–Alder reaction of o-quinodimethanes by utilizing tartaric acid ester as a chiral auxiliary

Y. Ukaji, K. Inomata, Motoki Takinami, 2006 .

The First Enantioselective Hetero Diels-Alder Reaction of Nitroso Compound Utilizing Tartaric Acid Ester as a Chiral Auxiliary

S. Fujinami, Y. Ukaji, K. Inomata, 2003 .

Enantioselective Synthesis of Lythraceae Alkaloid Lasubine II via Optically Active 2-Isoxazoline

Y. Ukaji, K. Inomata, T. Yamada, 2000 .

"Syn Effect" in the 1,4-Eliminative Ring Opening of [3-Substituted (E)-1-Propenyl]oxiranes to the Corresponding 2,4-Dienyl Alcohols

H. Takenaka, Y. Ukaji, K. Inomata, 2005 .

"Syn-Effect" in the Conversion of (E)-α, β-Unsaturated Esters to the Corresponding β, γ-Unsaturated Esters

A. Shibayama, Y. Ukaji, K. Inomata, 2003 .

Asymmetric hetero diels-alder reaction of nitroso compounds utilizing tartaric acid ester as a chiral auxiliary

S. Fujinami, Y. Ukaji, K. Inomata, 2008 .

The First Enantioselective Hetero Diels—Alder Reaction of Nitroso Compound Utilizing Tartaric Acid Ester as a Chiral Auxiliary.

S. Fujinami, Y. Ukaji, K. Inomata, 2003 .

Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions Utilizing Tartaric Acid Ester as a Chiral Auxiliary

Y. Ukaji, K. Inomata, 2003 .

Enantioselective Synthesis of Lythraceae Alkaloid Lasubine II via Optically Active 2-Isoxazoline.

Y. Ukaji, K. Inomata, Masaki Ima, 2000 .

“Syn Effect” in the 1,4-Eliminative Ring Opening of [3-Substituted (E)-1-Propenyl]oxiranes to the Corresponding 2,4-Dienyl Alcohols.

Y. Ukaji, K. Inomata, Naohiro Takeda, 2006 .

“Syn-Effect” in the Desulfonylation Reaction of α,α-Dialkylated (E)-Allylic Sulfones

A. Shibayama, H. Kinoshita, Y. Ukaji, 1997 .

“Syn-Effect” in the Conversion of (E)-α,β-Unsaturated Esters to the Corresponding β,γ-Unsaturated Esters.

A. Shibayama, Y. Ukaji, K. Inomata, 2003 .

Green/red cyanobacteriochromes regulate complementary chromatic acclimation via a protochromic photocycle

M. Ikeuchi, R. Narikawa, Yuu Hirose, 2013, Proceedings of the National Academy of Sciences.

Asymmetric Bis(alkoxycarbonylation) Reaction of Cyclic Olefins Catalyzed by Palladium in the Presence of Copper(I) Triflate

S. Fujinami, Y. Ukaji, K. Inomata, 2007 .

Efficient synthesis of benzothiophenes by [4+1] cycloaddition of 2-mercaptobenzaldehyde derivatives with isocyanides

T. Soeta, S. Fujinami, Y. Ukaji, 2016 .

Ugi‐type Multicomponent Reaction of Nitrile Imines, Isocyanides, and Isocyanates: Effective Synthesis of 1,2,4‐Triazinedione Derivatives

Y. Sakata, T. Soeta, Y. Ukaji, 2016 .

O-silylative Passerini reaction: a new one-pot synthesis of α-siloxyamides.

T. Soeta, Y. Ukaji, K. Inomata, 2010, Organic letters.

A New Aerobic Oxidation System Using Pd-Cu Catalysts in the Presence of CO

H. Kinoshita, Y. Ukaji, K. Inomata, 1994 .

A New Aerobic Oxidation System Using Pd-Cu Catalysts in the Presence of CO.

H. Kinoshita, Y. Ukaji, K. Inomata, 1995 .

The Lewis Acid-Catalyzed [3 + 1 + 1] cycloaddition of Azomethine Ylides with Isocyanides.

T. Soeta, S. Fujinami, Y. Ukaji, 2015 .

Regioselective Oxidation of Pyrrole Derivatives with DDQ and Its Synthetic Application

Y. Ukaji, K. Inomata, Ryoji Iwamoto, 2010 .

Catalytic Asymmetric Addition of Dialkylzinc to 3,4-Dihydroisoquinoline N-Oxides Utilizing Tartaric Acid Ester as a Chiral Auxiliary

Alauddin Ahmed, Y. Ukaji, K. Inomata, 2000 .

Phosphinic acid-promoted addition reaction of isocyanides to (Z)-hydroximoyl chlorides: efficient synthesis of α-(hydroxyimino)amides.

Y. Sakata, T. Soeta, Y. Ukaji, 2016, Organic & biomolecular chemistry.

Discovery of a novel unsymmetrical structural class of HCV NS5A inhibitors with low picomolar antiviral activity.

Y. Ukaji, K. Maeda, Y. Komoda, 2019, Bioorganic & medicinal chemistry letters.

N‐Heterocyclic Carbene Catalyzed Oxidative Coupling of Aldehydes with Carbodiimides under Aerobic Conditions: Efficient Synthesis of N‐Acylureas.

T. Soeta, S. Fujinami, Y. Ukaji, 2013 .

Asymmetric Bis(alkoxycarbonylation) Reaction of Terminal Olefins Catalyzed by Palladium in the Presence of Copper(I) Triflate and a Chiral Bioxazoline Ligand

Y. Ukaji, K. Inomata, S. Takeuchi, 2001 .

Direct and Unified Access to Carbon Radicals from Aliphatic Alcohols by Cost-Efficient Titanium-Mediated Homolytic C-OH Bond Cleavage.

Y. Ukaji, T. Suga, Yuuki Takahashi, 2022, Angewandte Chemie.

From‐Neutral‐to‐Neutral Reductive Radical Coupling of Non‐Activated Alcohols and Styrenes

Y. Ukaji, T. Suga, Chinatsu Miki, 2023, ChemistryEurope.

Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to an Achiral Allyl Alcohol Utilizing Diisopropyl Tartrate as a Chiral Auxiliary

M. Shimizu, Y. Ukaji, K. Inomata, 1996 .

Development of the Asymmetric Cycloaddition Reactions and Asymmetric Nucleophilic Addition Reaction Utilizing Tartaric Acid Esters

Y. Ukaji, K. Inomata, 1998 .

Enantioselective Synthesis of 2-Isoxazolines via Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxide to Achiral Allyl Alcohol

Y. Ukaji, K. Inomata, InomataKatsuhiko, 1993 .

Diastereoselective Construction of 2,2,6-Trisubstituted Tetrahydropyrans by Intramolecular Alkylation Reaction of Lithium Enolates Generated from α-Alkoxy Carboxylates

Y. Okumura, Y. Ukaji, Kazuhisa Morita, 1992 .

N-heterocyclic carbene catalyzed oxidative coupling of aldehydes with carbodiimides under aerobic conditions: efficient synthesis of N-acylureas.

T. Soeta, S. Fujinami, Y. Ukaji, 2013, Organic letters.

Green/red light-sensing mechanism in the chromatic acclimation photosensor

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