H. Fujioka

发表

Preparation of THP-ester-derived pyridinium-type salts and their reactions with various nucleophiles.

H. Fujioka, Yutaka Minamitsuji, Takahiro Moriya, 2012, Chemistry, an Asian journal.

Syntheses of Anthracyclines and Fredericamycin A via Strong Base-Induced CycloadditionReaction of Homophthalic Anhydrides

Y. Kita, H. Fujioka, 2007 .

In situ protection methodology in carbonyl chemistry.

H. Fujioka, Kenzo Yahata, 2014, Chemical & pharmaceutical bulletin.

Metal-free C-H cross-coupling toward oxygenated naphthalene-benzene linked biaryls.

K. Morimoto, T. Dohi, Y. Kita, 2011, Organic letters.

Ligand-free Suzuki–Miyaura coupling using ruthenium(0) nanoparticles and a continuously irradiating microwave system

Y. Tamenori, T. Honma, M. Arisawa, 2017 .

Hypervalent iodine(III)/Et4N+Br− combination in water for green and racemization-free aqueous oxidation of alcohols

T. Dohi, Y. Kita, H. Fujioka, 2009 .

Self‐Assembled Multilayer‐Stabilized Nickel Nanoparticle Catalyst for Ligand‐Free Cross‐Coupling Reactions: in situ Metal Nanoparticle and Nanospace Simultaneous Organization

S. Shuto, Y. Tamenori, T. Honma, 2016 .

Development of an Enyne Metathesis/Isomerization/Diels-Alder One-Pot Reaction for the Synthesis of a Novel Near-Infrared (NIR) Dye Core.

H. Aoyama, Y. Fujii, T. Uno, 2015, Chemistry.

A double iodoetherification of sigma-symmetric diene acetals for installing four stereogenic centers in a single operation: short asymmetric total synthesis of rubrenolide.

Y. Kita, Yusuke Ohba, H. Fujioka, 2005, Angewandte Chemie.

First Asymmetric Total Synthesis and Insight into the Structure of Laurenidificin

Tetsuya Kobayashi, M. Arisawa, Michinori Sumimoto, 2017 .

Versatile and chemoselective synthesis of fluorinated methyl ethers from methoxymethyl ethers

H. Fujioka, T. Maegawa, Y. Yoshikawa, 2017 .

Hypervalent iodine(III): selective and efficient single-electron-transfer (SET) oxidizing agent

K. Morimoto, T. Dohi, Y. Kita, 2009 .

Metal-Free Nitrogen-Containing Polyheterocyclic Near-Infrared (NIR) Absorption Dyes: Synthesis, Absorption Properties, and Theoretical Calculation of Substituted 5-Methylisoindolo[2,1-a]quinolines

T. Takagi, N. Kawashita, Y. Fujii, 2019, ACS omega.

Pd-Catalyzed Migratory Cycloisomerization of N-Allyl- o-allenylaniline Derivatives.

H. Aoyama, M. Arisawa, H. Fujioka, 2019, Organic letters.

Chemoselective Transformations of Aromatic Methoxymethyl Ethers Using Trialkylsilyl Triflate and 2,2′-Bipyridyl

M. Arisawa, H. Fujioka, Kenichi Murai, 2019, ACS omega.

Nickel Nanoparticle-catalyzed Carboxylation of Unsaturated Hydrocarbon with CO2 Using Sulfur-modified Au-supported Nickel Material

S. Shuto, M. Arisawa, Nozomi Saito, 2019, Chemistry Letters.

Reusable Immobilized Iron(II) Nanoparticle Precatalysts for Ligand-Free Kumada Coupling

Y. Tamenori, K. Tsuruta, T. Honma, 2018, ACS Applied Nano Materials.

Intramolecular iodoetherification of ene or diene ketals: facile synthesis of spiroketals.

Y. Kita, H. Fujioka, Hideki Hirose, 2011, Chemical communications.

Designer μ-oxo-bridged hypervalent iodine(III) organocatalysts for greener oxidations.

T. Dohi, Y. Kita, H. Fujioka, 2010, Chemical communications.

A mild and efficient one-pot synthesis of 2-dihydroimidazoles from aldehydes

Y. Kita, Yusuke Ohba, H. Fujioka, 2005 .

Chemical Transformation of Terpenoids. VI. Syntheses of Chiral Segments, Key Building-Blocks for the Left Half of Taxane-Type Diterpenoids

I. Kitagawa, H. Fujioka, Yoshio Yamamoto, 1984 .

Successive methyl migrations occurring in the acid treatment of 1-epoxyethyl-1,2,2-trimethyl-cyclopentane derivative

T. Hakoshima, K. Kitamura, I. Kitagawa, 1980 .

Concise asymmetric synthesis of a model compound, (4S,5S,6S)-6-(2,2-dimethoxy)ethyl-4,5-epoxy-6-hydroxy-2-cyclohexenone, for the cyclohexenone core of scyphostatin

Y. Kita, Y. Sawama, Naoyuki Kotoku, 2002 .

Stereoselective Construction of 1β-Azide- and 1β-Cyano-2-deoxyribose Derivatives

Y. Ueyama, H. Fujioka, Yutaka Minamitsuji, 2015 .

The rearrangement of 2,3-epoxysulfonates and its application to natural products syntheses: formal synthesis of (-)-aphanorphine and total syntheses of (-)-alpha-herbertenol and (-)-herbertenediol.

Y. Kita, Y. Sawama, Yusuke Ohba, 2003, The Journal of organic chemistry.

Recent Progress in Organocatalytic Asymmetric Halocyclization

H. Fujioka, Kenichi Murai, 2013 .

Nonmetathesis Heterocycle Formation by Ruthenium-Catalyzed Intramolecular [2 + 2] Cycloaddition of Allenamide-enes to Azabicyclo[3.1.1]heptanes

S. Shuto, Takashi Matsumoto, M. Arisawa, 2016 .

Asymmetric desymmetrization based on an intramolecular haloetherification: a highly effective and recyclable chiral nonracemic auxiliary, 2-exo-methyl-3-endo-phenyl-5-norbornene-2-carboxaldehyde, for meso-1,3- and meso-1,4-diols.

Y. Kita, Naoyuki Kotoku, Yasushi Nagatomi, 2004, Chemistry.

Desymmetrization of unsaturated meso-1,2-diols via an intramolecular haloetherification of ene acetals: A remarkable kinetic control

Y. Kita, Naoyuki Kotoku, Yasushi Nagatomi, 1998 .

Mild and efficient removal of hydroxyethyl unit from 2-hydroxyethyl ether derivatives leading to alcohols.

Y. Kita, Yusuke Ohba, H. Fujioka, 2005, Organic letters.

Unusual ipso substitution of diaryliodonium bromides initiated by a single-electron-transfer oxidizing process.

K. Morimoto, T. Dohi, Y. Kita, 2010, Angewandte Chemie.

Metal-free regioselective oxidative biaryl coupling leading to head-to-tail bithiophenes: reactivity switching, a concept based on the iodonium(III) intermediate.

K. Morimoto, T. Dohi, Y. Kita, 2010, Organic letters.

Organic synthesis using a hypervalent iodine reagent: unexpected and novel domino reaction leading to spiro cyclohexadienone lactones.

Y. Kita, H. Komatsu, H. Fujioka, 2010, Chemical communications.

Clean and efficient benzylic C-H oxidation in water using a hypervalent iodine reagent: activation of polymeric iodosobenzene with KBr in the presence of montmorillonite-K10.

T. Dohi, Y. Kita, H. Fujioka, 2008, The Journal of organic chemistry.

Metal-Free C—H Cross-Coupling Toward Oxygenated Naphthalene-Benzene Linked Biaryls.

K. Morimoto, T. Dohi, Y. Kita, 2012 .

Metal-Free Regioselective Oxidative Biaryl Coupling Leading to Head-to-Tail Bithiophenes: Reactivity Switching, a Concept Based on the Iodonium(III) Intermediate

K. Morimoto, T. Dohi, Y. Kita, 2010 .

Phenyliodine diacetate-mediated oxidative cleavage of cyclobutanols leading to γ-hydroxy ketones

Y. Kita, H. Komatsu, H. Fujioka, 2011 .

Synthesis of antitumor marine alkaloid discorhabdin A oxa analogues.

Y. Kita, H. Fujioka, Daigo Kamimura, 2009, Organic letters.

Facile and efficient synthesis of lactols by a domino reaction of 2,3-epoxy alcohols with a hypervalent iodine(III) reagent and its application to the synthesis of lactones and the asymmetric synthesis of (+)-tanikolide.

Y. Kita, S. Matsuda, H. Fujioka, 2007, Chemistry.

Ruthenium-Catalyzed 1,6-Aromatic Enamide-Silylalkyne Cycloisomerization: Approach to 2,3-Disubstituted Indoles.

M. Arisawa, H. Fujioka, Shohei Ohno, 2017, The Journal of organic chemistry.

Cycloisomerization between Aryl Enol Ether and Silylalkynes under Ruthenium Hydride Catalysis: Synthesis of 2,3-Disubstituted Benzofurans.

M. Arisawa, H. Fujioka, Shohei Ohno, 2017, Organic letters.

One‐Pot Olefin Isomerization/Aliphatic Enamine Ring‐Closing Metathesis/Oxidation/1,3‐Dipolar Cycloaddition for the Synthesis of Isoindolo[1,2‐a]isoquinolines

S. Shuto, Y. Fujii, M. Arisawa, 2015 .

ORGANIC SYNTHESIS UTILIZING BECKMANN FRAGMENTATION : ASYMMETRIC CARBON-CARBON BOND FORMATION VIA CHIRAL ACETAL INTERMEDIATES

Y. Kita, H. Fujioka, H. Kitagawa, 1992 .

Asymmetric total synthesis of clavolonine.

Y. Kita, H. Fujioka, Kenji Nakahara, 2011, Organic letters.

Oxidative Rearrangement via in Situ Generated N-Chloroamine: Synthesis of Fused Tetrahydroisoquinolines.

H. Aoyama, H. Fujioka, Kenichi Murai, 2016, Organic letters.

One-pot three-component reaction providing 1,5-benzodiazepine derivatives

Y. Kita, H. Fujioka, Kenichi Murai, 2008 .

Method for the efficient synthesis of highly-substituted oxetan- and azetidin-, dihydrofuran- and pyrrolidin-3-ones and its application to the synthesis of (±)-pseudodeflectusin.

H. Fujioka, T. Maegawa, A. Goto, 2012, Organic letters.

Direct conversion of acetals to esters with high regioselectivity via O,P-acetals.

H. Fujioka, T. Maegawa, A. Goto, 2011, Organic & biomolecular chemistry.

Remarkable effect of CF3CH2OH for the halogen induced oxidative rearrangement reaction of aminals leading to 3,4-dihydroquinazolines.

Daisuke Endo, H. Fujioka, Kenichi Murai, 2013, Organic & biomolecular chemistry.

Oxidative rearrangement of spiro cyclobutane cyclic aminals: efficient construction of bicyclic amidines.

H. Komatsu, H. Fujioka, Kenichi Murai, 2012, Organic letters.

New Three-Component Reaction: Novel Formation of a Seven-Membered Ring by the Unexpected Reaction at the γ-Position of the β-Keto Ester

Y. Kita, H. Fujioka, Ozora Kubo, 2007 .

The synthetic and biological studies of discorhabdins and related compounds.

K. Morimoto, Y. Kita, T. Shibata, 2011, Organic & biomolecular chemistry.

Chemoselective Nucleophilic Functionalizations of Aromatic Aldehydes and Acetals via Pyridinium Salt Intermediates.

Y. Sawama, H. Sajiki, Takahiro Kawajiri, 2019, The Journal of organic chemistry.

Total synthesis of a fully protected palytoxin carboxylic acid

J. B. White, M. Martinelli, W. Christ, 1989 .

Total Synthesis of Palytoxin Carboxylic Acid and Palytoxin Amide

W. Christ, R. W. Armstrong, H. Fujioka, 1989 .

One-pot synthesis of imidazolines from aldehydes: detailed study about solvents and substrates

Y. Kita, Yusuke Ohba, H. Fujioka, 2007 .

A simple and efficient radical reduction using water-soluble radical initiator and hypophosphorous acid in aqueous alcohol

Y. Kita, H. Nambu, H. Fujioka, 2004 .

Isolation and characterization of a new 5-aminofurylthiazole from the catalytic reduction of 4-(5-nitro-2-furyl)thiazole.

S. Swaminathan, S. Hibino, G. Bryan, 1985, Chemical & pharmaceutical bulletin.

Intramolecular bromo-amination of 1,4-cyclohexadiene aminal: one-pot discrimination of two olefins and concise asymmetric synthesis of (-)-gamma-lycorane.

Y. Kita, Yusuke Ohba, H. Fujioka, 2006, Chemical communications.

Asymmetric Total Synthesis of Fredericamycin A.

Y. Kita, S. Akai, S. Kitagaki, 1999, Angewandte Chemie.

Asymmetric synthesis of anthracyclinones : synthesis of a new chiral AB-synthon, (5R,6R)-6-ethyl-5,6-dihydroxy-5,6,7,8-tetrahydro-1,4-naphthoquinone, and its application for a novel regioselective synthesis of (-)-γ-rhodomycinone

Y. Kita, H. Annoura, H. Fujioka, 1992 .

The reaction of acetal-type protective groups in combination with TMSOTf and 2,2′-bipyridyl; mild and chemoselective deprotection and direct conversion to other protective groups

H. Fujioka, Yutaka Minamitsuji, Ozora Kubo, 2011 .

A highly efficient macrolactonization method via ethoxyvinyl ester.

Y. Kita, Yusuke Ohba, H. Fujioka, 2009, Chemistry.

Enantioselective, desymmetrizing, bromolactonization reactions of symmetric olefinic dicarboxylic acids.

A. Nakamura, H. Fujioka, Kenichi Murai, 2014, Chemistry, an Asian journal.

Acid-Promoted Rearrangement of Cyclic α,β-Epoxy Acylates: Stereoselective Synthesis of Spirocyclanes and Quaternary Carbon Centers

M. Kondo, Y. Kita, S. Akai, 1997 .

Acid-promoted rearrangement of α,β-epoxy acylates: Remarkable effects of an acyl group and a Lewis acid

Y. Kita, S. Kitagaki, H. Fujioka, 1997 .

Asymmetric synthesis of chiral spirocyclanes: A new route to the optically active spiro[cyclopentane-1,1′-indan]-2,5-dione system

Y. Kita, S. Akai, S. Kitagaki, 1996 .

Asymmetric synthesis of chiral spirocyclanes: Selective formation of 2-acyloxy-1-oxospiro[4.n]alkanes by regio- and stereoselective rearrangement of α,β-epoxy acylates in bicyclo[n.3.0]alkane systems

Yutaka Yoshida, Hiromichi Fujioka, M. Kondo, 1995 .

Enantioselective iodolactonization of allenoic acids.

H. Fujioka, Kenichi Murai, Nozomi Shimizu, 2014, Chemical communications.

Asymmetric bromolactonization catalyzed by a C3-symmetric chiral trisimidazoline.

A. Nakamura, H. Fujioka, Tomoyo Matsushita, 2010, Angewandte Chemie.

Remarkable effect of phosphine on the reactivity of O,P-acetal--efficient substitution reaction of O,P-acetal.

Y. Sawama, H. Fujioka, Ozora Kubo, 2010, Chemical communications.

Mild deprotection of methylene acetals in combination with trimethylsilyl triflate-2,2'-bipyridyl.

H. Fujioka, Yutaka Minamitsuji, Ozora Kubo, 2010, Chemical & pharmaceutical bulletin.

Remarkable effect of 2,2'-bipyridyl: mild and highly chemoselective deprotection of methoxymethyl (MOM) ethers in combination with TMSOTf (TESOTf)-2,2'-bipyridyl.

H. Fujioka, Yutaka Minamitsuji, Ozora Kubo, 2009, Chemical communications.

Organic Chemistry Using Weakly Electrophilic Salts: The Reaction with Nitrogen Nucleophiles

Y. Kita, H. Fujioka, K. Okamoto, 2009 .

Mild and efficient deprotection of acetal-type protecting groups of hydroxyl functions by triethylsilyl triflate: 2,4,6-collidine combination

H. Fujioka, K. Okamoto, Ozora Kubo, 2009 .

Organic chemistry using weakly electrophilic salts: efficient formation of O,O-mixed, O,S- and N,O-acetals.

Y. Kita, Y. Sawama, Ruichuan Li, 2007, The Journal of organic chemistry.

Alkyl- and arylation of oxacyclic ethers with triethylsilyl triflate-2,4,6-collidine-Gilman reagent combination: remarkable discrimination of two ether oxygens

Y. Kita, Y. Sawama, H. Fujioka, 2007 .

Reaction of Tetrahydropyranyl Ethers with Triethylsilyl Trifluoromethanesulfonate–2,4,6‐Collidine Combination: Speculation on the Intermediate, Efficient Deprotection, and Application to Efficient Ring‐Closing Metathesis as a Tether

Y. Kita, Y. Sawama, H. Fujioka, 2007 .

Highly Chemoselective Alkylation of Acetals Using TESOTf-2,4,6-Collidine-Gilman Reagent Combination

Y. Kita, Y. Sawama, H. Fujioka, 2006 .

Reaction of the acetals with TESOTf-base combination; speculation of the intermediates and efficient mixed acetal formation.

Y. Kita, Y. Sawama, Ruichuan Li, 2006, Journal of the American Chemical Society.

Unexpected highly chemoselective deprotection of the acetals from aldehydes and not ketones: TESOTf-2,6-lutidine combination.

Y. Kita, Y. Sawama, S. Matsuda, 2004, Journal of the American Chemical Society.

Asymmetric synthesis using C2-symmetric diols: Use of (5R,6R)-3-acetoxy-5,6-diphenyl-1,4-dioxan-2-one as a chiral synthetic equivalent of 1,2-ethanediol 1,2-dicarbocation

M. Kondo, Y. Kita, N. Matsunaga, 1995 .

New three-component reaction: novel formation of a seven-membered ring by the unexpected reaction at the gamma-position of the beta-keto ester.

Y. Kita, Yusuke Ohba, H. Fujioka, 2007, Organic letters.

Transformation of Methylene Acetals to Bromoformates with a Combination of Trimethyl(phenylthio)silane and N-Bromosuccinimide.

A. Nakamura, H. Fujioka, T. Maegawa, 2017, The Journal of organic chemistry.

Cerium ammonium nitrate (CAN) for mild and efficient reagent to remove hydroxyethyl units from 2-hydroxyethyl ethers and 2-hydroxyethyl amines

Y. Kita, Yusuke Ohba, H. Fujioka, 2007 .

C3-Symmetric chiral trisimidazoline-catalyzed Friedel-Crafts (FC)-type reaction.

S. Takizawa, H. Sasai, S. Hirata, 2014, Organic & biomolecular chemistry.

Tandem β-Enamino Ester Formation and Cyclization with o-Alkynyl Anilines Catalyzed by InBr3: Efficient Synthesis of β-(N-Indolyl)-α,β-unsaturated Esters.

Y. Kita, H. Fujioka, Kenichi Murai, 2009 .

Tandem beta-enamino ester formation and cyclization with o-alkynyl anilines catalyzed by InBr3: efficient synthesis of beta-(N-indolyl)-alpha,beta-unsaturated esters.

Y. Kita, H. Fujioka, Kenichi Murai, 2009, The Journal of organic chemistry.

SnCl4-promoted rearrangement of 2,3-epoxy alcohol derivatives: stereochemical control of the reaction

Y. Kita, S. Matsuda, H. Fujioka, 2005 .

Methylene acetal formation from 1,2- and 1,3-diols using an O,S-acetal, 1,3-dibromo-5,5-dimethylhydantoin, and BHT.

H. Fujioka, T. Maegawa, Y. Koutani, 2013, The Journal of organic chemistry.

Facile preparation of oxazole-4-carboxylates and 4-ketones from aldehydes using 3-oxazoline-4-carboxylates as intermediates.

H. Komatsu, H. Fujioka, Tomoyo Matsushita, 2010, Organic letters.

Remarkable effect of CF3CH2OH for the halogen induced oxidative rearrangement reaction of aminals leading to 3,4-dihydroquinazolines.

Daisuke Endo, H. Fujioka, Kenichi Murai, 2013, Organic & biomolecular chemistry.

Oxidative decarboxylative synthesis of 2-H-imidazolines from glyoxylic acid and 1,2-diamines.

Y. Kita, H. Fujioka, Kenichi Murai, 2008, Chemical communications.

Concise total synthesis of (-)-spongotine A.

Y. Kita, H. Fujioka, Ozora Kubo, 2007, The Journal of organic chemistry.

Enantio- and Diastereoselective Betti/aza-Michael Sequence: Single Operated Preparation of Chiral 1,3-Disubstituted Isoindolines.

S. Takizawa, H. Sasai, Kenta Kishi, 2017, Organic letters.

Asymmetric total synthesis of (-)-stenine and 9a-epi-stenine.

Y. Kita, Y. Sawama, Naoyuki Kotoku, 2012, Chemistry.

New Three‐Component Reaction: Novel Formation of a Seven‐Membered Ring by the Unexpected Reaction at the γ‐Position of the β‐Keto Ester.

Y. Kita, Yusuke Ohba, H. Fujioka, 2007 .

One‐Pot Synthesis of Imidazolines from Aldehydes: Detailed Study about Solvents and Substrates.

Y. Kita, Yusuke Ohba, H. Fujioka, 2007 .

Enantioselective total synthesis of a potent antitumor antibiotic, fredericamycin A.

Y. Kita, S. Akai, S. Kitagaki, 2001, Journal of the American Chemical Society.

Stereocontrol Between Remote Atom Centers Using Chiral Acetals and Its Application to Asymmetric Syntheses of Natural Products

Y. Kita, H. Fujioka, 2009 .

[Development of highly stereoselective reactions using lone pairs of oxygen atoms].

H. Fujioka, 2005, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Asymmetric Synthesis Using Chiral Acetals from C2-Symmetric Diols and Its Application to Natural Product Synthesis

Y. Kita, H. Fujioka, 1994 .

Asymmetric Synthesis Using Chiral Acetals : Highly Stereoselective Reduction of Chiral α-Keto-β, γ-unsaturated Acetals and Its Application for the Synthesis of (R)-(-)- and (S)-(+)-3'-Methoxy-4'-O-methyljoubertiamine

Y. Kita, H. Annoura, H. Fujioka, 1989 .

Asymmetric Synthesis Using Chiral Acetals : Highly Diastereoselective Nucleophilic Addition of Grignard Reagents to Chiral 1-Oxo-β-tetralone 1-Acetals

Y. Kita, H. Annoura, H. Fujioka, 1989 .

Asymmetric Synthesis Using Chiral Acetals : Highly Diastereoselective Addition of Organocerium Reagents to Chiral α-Aldoxime-Ether Acetal

Y. Kita, H. Annoura, H. Fujioka, 1989 .

Asymmetric synthesis of anthracyclinones using chiral acetal: synthesis of a new chiral AB-synthon, ()-2-bromo-6-ethynyl-6-hydroxy-5, 6, 7, 8-tetrahydro-1, 4-naphthoquinone, and its application for ()-7-deoxydaunomycinone

Y. Kita, H. Annoura, H. Fujioka, 1987 .

Asymmetric synthesis using chiral acetals. Studies on the nucleophilic addition of organometallics to chiral .ALPHA.-keto acetals in open-chain systems.

H. Annoura, H. Fujioka, Y. Tamura, 1987 .

Asymmetric synthesis using chiral acetals: Studies on the nucleophilic addition of organometallics to chiral x-keto acetals in cyclic systems.

H. Annoura, H. Fujioka, Y. Tamura, 1987 .

Highly stereoselective reduction of chiral α-keto-β, γ-unsaturated acetals: Synthesis of both epimeric allyl alcohols by proper choice of additive

H. Annoura, H. Fujioka, Y. Tamura, 1987 .

Diastereoselective addition of grignard reagents to chiral α-ketoacetals

H. Annoura, H. Fujioka, Y. Tamura, 1986 .

Diastereoselective nucleophilic addition to chiral open-chain α-ketoacetals: Synthesis of (R)- and (S)-mevalolactone

H. Annoura, H. Fujioka, Y. Tamura, 1986 .

Stereoselective Construction of 2,7-Disubstituted fused-Bis Tetrahydrofuran Skeletons: Biomimetic-Type Synthesis and Biological Evaluation of (±)- and (-)-Aplysiallene and Their Derivatives.

Kuniaki Suzuki, M. Arisawa, H. Fujioka, 2015, The Journal of organic chemistry.

The first asymmetric total syntheses of both enantiomers of cryptocaryone

Y. Kita, H. Fujioka, Kenji Nakahara, 2010 .

A chiral hypervalent iodine(III) reagent for enantioselective dearomatization of phenols.

T. Dohi, Y. Kita, H. Fujioka, 2008, Angewandte Chemie.

Concise asymmetric total synthesis of scyphostatin, a potent inhibitor of neutral sphingomyelinase.

Y. Kita, Y. Sawama, Naoyuki Kotoku, 2007, Chemistry.

Asymmetric dearomatizing spirolactonization of naphthols catalyzed by spirobiindane-based chiral hypervalent iodine species.

T. Dohi, Y. Kita, M. Shiro, 2013, Journal of the American Chemical Society.

Asymmetric total synthesis of fredericamycin A: an intramolecular cycloaddition pathway.

Y. Kita, S. Akai, H. Fujioka, 2005, Chemistry.

Concise synthesis of oxacyclic compounds using highly discriminative two-way transformations of α,β-unsaturated esters in the presence of enones.

H. Aoyama, M. Arisawa, H. Fujioka, 2017, Chemical communications.

Stereochemistry of palytoxin. 4. Complete structure

J. M. Finan, Yoshito Kishi, W. Christ, 1982 .

Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals

H. Aoyama, M. Arisawa, H. Fujioka, 2020 .

C3-symmetric trisimidazoline-catalyzed enantioselective bromolactonization of internal alkenoic acids.

A. Nakamura, H. Fujioka, Tomoyo Matsushita, 2012, Chemistry.

C3-Symmetric chiral trisimidazoline: the role of a third imidazoline and its application to the nitro Michael reaction and the α-amination of β-ketoesters

A. Nakamura, H. Fujioka, Kenichi Murai, 2011 .

Selective Transformation of β‐Disubstituted Enones and Ynones in the Presence of β‐Monosubstituted Enones

H. Fujioka, Kentaro Morita, Reiya Ohta, 2018 .

In situ protection methodology for selective one-pot allylation and alkylation of ketones in the presence of α,β-unsaturated ketones

H. Fujioka, Kentaro Morita, Kenzo Yahata, 2016 .

Total synthesis of a new inhibitor of superoxide anion generation, opc-15161

Y. Kita, S. Akai, H. Fujioka, 1991 .

Lewis acid-promoted rearrangement of 2,3-epoxy alcohol derivatives: stereochemical control and selective formation of two types of chiral quaternary carbon centers from the single carbon skeleton.

Y. Kita, S. Matsuda, H. Fujioka, 2006, The Journal of organic chemistry.

Acid-promoted rearrangement of 2-aryl-2,3-epoxy acylates: construction of chiral benzylic quaternary carbon centers

Y. Kita, H. Fujioka, K. Higuchi, 2000 .

Efficient pinacol rearrangement mediated by trimethyl orthoformate

Y. Kita, H. Fujioka, K. Higuchi, 1997 .

Effects of phosphorus substituents on reactions of α-alkoxyphosphonium salts with nucleophiles.

Y. Sawama, H. Fujioka, Ozora Kubo, 2012, Chemistry.

C(3)-symmetric chiral trisimidazoline: design and application to organocatalyst.

H. Fujioka, Kenichi Murai, Yusuke Takahara, 2010, Organic letters.

The first total synthesis of prianosin B

Y. Kita, H. Fujioka, Daigo Kamimura, 2009 .

Enhanced Reactivity of [Hydroxy(tosyloxy)iodo]benzene in Fluoroalcohol Media. Efficient Direct Synthesis of Thienyl(aryl)iodonium Salts

T. Dohi, Y. Kita, Nobutaka Yamaoka, 2010, Molecules.

Concise asymmetric synthesis of (−)-herbertenediol

Y. Kita, Y. Sawama, Yusuke Ohba, 2003 .

2,5-cis-2,3,5-Trisubstituted tetrahydrofurans from the diastereomixture of 2,4-disubstituted 1,3-dioxepins via stereomutation.

H. Fujioka, Ozora Kubo, Kenzo Yahata, 2011, Chemical communications.

A Mild and Versatile Method for the Synthesis of Alkyl Ethers from Methoxymethyl Ethers and Application to the Preparation of Sterically Crowded Ethers

Y. Ueyama, H. Fujioka, Yutaka Minamitsuji, 2012 .

Study of the Lewis acid-promoted rearrangement of 2-aryl-2,3-epoxy acylates

Y. Kita, H. Fujioka, K. Higuchi, 2001 .

Regio- and stereoselective rearrangement reactions of various α,β-epoxy acylates: Suitable combination of acyl groups and Lewis acids

Y. Kita, S. Kitagaki, Y. Yoshida, 1999 .

Design, Synthesis, and Monoamine Oxidase Inhibitory Activity of (+)-Cinchonaminone and Its Simplified Derivatives.

S. Shuto, H. Aoyama, M. Arisawa, 2021, ACS medicinal chemistry letters.

Kinetic resolution of β-substituted olefinic carboxylic acids by asymmetric bromolactonization.

A. Nakamura, H. Fujioka, Tomoyo Matsushita, 2013, Organic letters.

Non-dehydrative pinacol rearrangement using a Lewis acid-trialkyl orthoester combined system

Y. Kita, Y. Yoshida, H. Fujioka, 1998 .

Domino reaction of 2,3-epoxy-1-alcohols and PIFA in the presence of H2O and the concise synthesis of (+)-tanikolide.

Y. Kita, S. Matsuda, H. Fujioka, 2005, Angewandte Chemie.

Aromatic aldehyde-selective aldol addition with aldehyde-derived silyl enol ethers.

Y. Sawama, H. Sajiki, Takahiro Kawajiri, 2018, Chemical communications.

Chemoselective Reduction and Alkylation of Carbonyl Functions Using Phosphonium Salts as an in Situ Protecting Groups.

H. Fujioka, Reiya Ohta, 2017, Chemical & pharmaceutical bulletin.

Selective transformations of carbonyl functions in the presence of α,β-unsaturated ketones: concise asymmetric total synthesis of decytospolides A and B.

H. Fujioka, Kenzo Yahata, M. Minami, 2014, Organic letters.

Clean and Direct Synthesis of α,α′-Bithiophenes and Bipyrroles by Metal-Free Oxidative Coupling Using Recyclable Hypervalent Iodine(III) Reagents

K. Morimoto, T. Dohi, Y. Kita, 2009 .

Synthesis of the Marine Pyrroloiminoquinone Alkaloids, Discorhabdins

Y. Kita, H. Fujioka, Yasufumi Wada, 2010, Marine drugs.

Development of a Sulfur-Modified Glass-Supported Pd Nanoparticle Catalyst for Suzuki-Miyaura Coupling.

S. Shuto, Y. Tamenori, T. Honma, 2016, Chemical & pharmaceutical bulletin.

Selective Formation of trans/threo/cis and cis/threo/cis Bis-Tetrahydrofurans from the Same Diene Diols

Y. Kita, H. Fujioka, Kenichi Murai, 2014 .

Stereoselective synthesis of cis-2,5-disubstituted THFs: application to adjacent bis-THF cores of Annonaceous acetogenins.

H. Fujioka, Shintaro Wakamatsu, Kenji Nakahara, 2012, Organic letters.

Facile formation of tetrahydrofurans with multiple chiral centers using double iodoetherification of σ-symmetric diene acetals : short asymmetric total synthesis of rubrenolide and rubrynolide

Y. Kita, Yusuke Ohba, H. Fujioka, 2008 .

Stereochemistry of palytoxin. Part 3. C7-C51 segment

W. Christ, Y. Kishi, D. Uemura, 1982 .

One-pot enyne metathesis/Diels-Alder/oxidation to six-membered silacycles with a multi-ring core: discovery of novel fluorophores.

Y. Fujii, T. Uno, M. Arisawa, 2017, Chemical communications.

Reactivity of the ester group attached isoxazoline, benzisoxazole, and isoxazole: a facial preparation of 3-acyl-substituted these heterocycles

H. Fujioka, Kenichi Murai, Shuji Miyazaki, 2012 .

Discovery and structure-activity relationship of imidazolinylindole derivatives as kallikrein 7 inhibitors.

Tsuyoshi Muto, H. Sugawara, H. Fujioka, 2019, Bioorganic & medicinal chemistry letters.

Organic synthesis utilizing Beckmann fragmentation: highly stereoselective C–C bond formation in the reaction of 2,3-isopropylidenedioxycyclohexanone oxime esters with organoaluminium reagents

M. Miyazaki, Y. Kita, H. Fujioka, 1993 .

Enantioselective organocatalytic oxidation of ketimine.

S. Takizawa, H. Sasai, Kenta Kishi, 2016, Organic & biomolecular chemistry.

Reversing the reactivity of carbonyl functions with phosphonium salts: enantioselective total synthesis of (+)-centrolobine.

Y. Sawama, H. Fujioka, Ozora Kubo, 2011, Angewandte Chemie.

Asymmetric Desymmetrization of Saturated and Unsaturated meso-1,2-Diols

Y. Kita, Naoyuki Kotoku, Yasushi Nagatomi, 2000 .

SYNTHESIS OF A CHIRAL 1,1,3-TRIMETHYLCYCLOHEXANE DERIVATIVE FROM d-CAMPHOR: A POTENT KEY BUILDING BLOCK FOR ENT-TAXANE-TYPE DITERPENOIDS

I. Kitagawa, H. Fujioka, A. Takagi, 1980 .

Kinetically controlled optical resolution of racemic norbornene aldehyde derivatives.

Y. Kita, Y. Sawama, Naoyuki Kotoku, 2003, Chirality.

Synthesis of 2,5-dioxygenated pyrazine 4-oxides: total synthesis of a new inhibitor of superoxide anion generation, OPC-15161

Y. Kita, S. Akai, H. Fujioka, 1994 .

Selective Deprotection of Methylene Acetal and MOM Ether in the Presence of Ketal-Type Protective Groups: Remarkable Effect of TBSOTf

H. Fujioka, Kenzo Yahata, T. Maegawa, 2012 .

A Simple and Efficient Radical Reduction Using Water‐Soluble Radical Initiator and Hypophosphorous Acid in Aqueous Alcohol.

Y. Kita, H. Nambu, H. Fujioka, 2005 .

STEREOCHEMISTRY OF PALYTOXIN. PART 4. COMPLETE STRUCTURE

J. M. Finan, W. Christ, Y. Kishi, 1983 .

Reaction of acetals with various carbon nucleophiles under non-acidic conditions: C-C bond formation via a pyridinium-type salt.

Y. Kita, Y. Sawama, H. Fujioka, 2012, Chemistry, an Asian journal.

Diastereotopic group selective intramolecular conjugate addition of 4-(2-hydroxyethyl)-p-quinol derivatives: Synthesis of the optically pure cis-7-oxabicyclo[4.3.0]non-2-en-4-one skeleton

Y. Kita, S. Kitagaki, H. Fujioka, 1994 .

New perspective for natural products synthesis: concise synthesis of (+)-sch 642305 by chiral auxiliary multiuse methodology.

Y. Kita, Yusuke Ohba, H. Fujioka, 2007, Organic letters.

Remote asymmetric induction for chiral 1,4-diols using a chiral acetal derived from chiral hydrobenzoin

Y. Kita, N. Matsunaga, Yasushi Nagatomi, 1996 .

The first total synthesis of a potent β-rhodonycin, oxaunonycin: regioselectiveglycosidation of the c-7 hydroxyl c-7 group of β-rhodomycinone

Y. Kita, H. Fujioka, H. Maeda, 1990 .

Marine Pyrroloiminoquinone Alkaloids, Makaluvamines and Discorhabdins, and Marine Pyrrole-Imidazole Alkaloids

Y. Kita, H. Fujioka, 2013 .

Marine pyrroloiminoquinone alkaloids.

Y. Kita, H. Fujioka, 2012, Topics in current chemistry.

A Mild and Efficient One‐Pot Synthesis of 2‐Dihydroimidazoles from Aldehydes.

Y. Kita, Yusuke Ohba, H. Fujioka, 2005 .

Diastereoselective Desymmetrization of Symmetric Dienes and its Synthetic Application

Kenji Nakahara, Hiromichi Fujioka, H. Fujioka, 2010, Symmetry.

Lattice Image Observations of Nanoscale Ordered Regions in Pb(Mg1/3Nb2/3)O3

Shoken Nagakari, H. Fujioka, Tsuneo Mishima, 1997 .

μ-Oxo-Bridged Hypervalent Iodine(III) Compound as an Extreme Oxidant for Aqueous Oxidations

T. Dohi, Y. Kita, Tomofumi Nakae, 2012 .

μ-Oxo-Bridged Hypervalent Iodine(III) Compound as an Extreme Oxidant for Aqueous Oxidations.

T. Dohi, Y. Kita, Tomofumi Nakae, 2012 .

Alkaloid Synthesis

M. Venturi, R. Naaman, D. Beratan, 2012 .

An unusual reaction of α-alkoxyphosphonium salts with Grignard reagents under an O2 atmosphere.

Y. Sawama, H. Fujioka, Ozora Kubo, 2011, Chemical communications.

Palladium-Catalyzed Seven-Membered Silacycle Construction: 1,7-Enyne Hydroxycyclization To Give a Benzosilepine Skeleton.

M. Arisawa, H. Fujioka, Shohei Yoshioka, 2018, Organic letters.

Asymmetric synthesis by the intramolecular haloetherification reaction of ene acetal: discrimination of prochiral dienes in cyclohexane systems.

Y. Kita, Y. Sawama, Naoyuki Kotoku, 2005, Chemical & pharmaceutical bulletin.

Oxidative Rearrangement of Secondary Amines Using Hypervalent Iodine(III) Reagent.

Tetsuya Kobayashi, M. Miyoshi, H. Fujioka, 2018, Organic letters.

Direct synthesis of dialkylarylvinylsilane derivatives: metathesis of dialkylaryl-iso-propenylsilane and its application to tetracyclic silacycle dye synthesis.

Y. Tsutsumi, T. Uno, M. Arisawa, 2019, Chemical communications.

1-Alkoxyvinyl Ester as an Excellent Acyl Donor: Efficient Macrolactone Synthesis.

Y. Kita, S. Akai, Tohru Kamitanaka, 2021, Journal of Organic Chemistry.

Enantioselective constructions of quaternary carbons and their application to the asymmetric total syntheses of fredericamycin A and discorhabdin A

Y. Kita, H. Fujioka, 2007 .

Hypervalent Iodine(III) Organocatalysts

T. Dohi, Y. Kita, H. Fujioka, 2010 .

Organoiodine-Catalyzed Oxidative Spirocyclization of Phenols using Peracetic Acid as a Green and Economic Terminal Oxidant

T. Dohi, Y. Kita, H. Fujioka, 2009 .

Hypervalent iodine(III) reagent-promoted rearrangement and subsequent oxidative ring cleavage of cyclic 2,3-epoxy-1-alcohol derivatives

Y. Kita, S. Kitagaki, S. Matsuda, 2005 .

Design and synthesis of N1,N8-diacetylspermidine analogues having a linker with desired functional groups.

M. Arisawa, A. Oguro, H. Fujioka, 2019, Organic & biomolecular chemistry.

Ligand-free Suzuki–Miyaura coupling using ruthenium(0) nanoparticles and a continuously irradiating microwave system

Y. Tamenori, M. Arisawa, Nozomi Saito, 2017 .

An efficient synthesis of peri-hydroxy aromatic compounds via a strong-base-induced

Y. Kita, S. Akai, H. Fujioka, 2000, The Journal of organic chemistry.

Regio- and stereo-selective construction of anthracyclinones: total synthesis of (–)-γ-rhodomycinone

Y. Kita, H. Annoura, H. Fujioka, 1989 .

Asymmetric dearomatizing spirolactonization of naphthols catalyzed by spirobiindane-based chiral hypervalent iodine species.

T. Dohi, Y. Kita, M. Shiro, 2013, Journal of the American Chemical Society.

Mouse Kallikrein 7 in complex with imidazolinylindole derivative

H. Fujioka, Yutaka Minamitsuji, Kenichi Murai, 2019 .