Mukaiyama Teruaki | Center For Basic Res. The Kitasato Inst.

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概要

• 同名の論文著者
• Center For Basic Res. The Kitasato Inst.の論文著者

関連著者

• Mukaiyama Teruaki

  Center For Basic Res. The Kitasato Inst.

• MUKAIYAMA Teruaki

  Center for Basic Research, The Kitasato Institute

• Mukaiyama Teruaki

  The Kitasato Institute Center For Basic Research

• Minowa Tomofumi

  Kitasato Institute For Life Sciences Kitasato University

• Mukaiyama T

  Center For Basic Research The Kitasato Institute

• Fujisawa Hidehiko

  Center For Basic Research The Kitasato Institute

• Minowa Tomofumi

  Center For Basic Research The Kitasato Institute

• FUJISAWA Hidehiko

  Center for Basic Research, The Kitasato Institute

• YAMANE Yoshinobu

  Center for Basic Research, The Kitasato Institute

• Yamane Yoshinobu

  Center For Basic Research The Kitasato Institute

• Kawano Yoshikazu

  Center For Basic Research The Kitasato Institute

• Tozawa Takashi

  Center For Basic Research The Kitasato Institute

• KAWANO Yoshikazu

  Center for Basic Research, The Kitasato Institute

• Takahashi Eiki

  Kitasato Institute For Life Sciences Kitasato University

• Ikegai Kazuhiro

  Center For Basic Research The Kitasato Institute

• TAKAHASHI Eiki

  Center for Basic Research, The Kitasato Institute (TCI)

• KURODA Kiichi

  Center for Basic Research, The Kitasato Institute

• Nagata Yuzo

  Center For Basic Research The Kitasato Institute

• Kuroda Kiichi

  Center For Basic Research The Kitasato Institute

• Funasaka Setsuo

  Center For Basic Research Kitasato Institute

• FUKUMOTO Kentarou

  Center for Basic Research, The Kitasato Institute

• Nagao Hitoshi

  Center For Basic Research The Kitasato Institute

• Fukumoto Kentarou

  Center For Basic Research The Kitasato Institute

• Funasaka Setsuo

  Center For Basic Res. The Kitasato Inst.

• Sato Yoshinori

  Center For Basic Research The Kitasato Institute

• HAYASHI Yujiro

  Department of Human and Mechanical Systems Engineering, Kanazawa Univ.

• Hayashi Yujiro

  Department Of Chemistry School Of Science The University Of Tokyo

• YANAI Tomoko

  Shinnikka Environmental Engineering Co. Ltd.

• Ogawa Yozo

  Department Of Applied Chemistry Faculty Of Engineering Okayama University Of Science

• IKEGAI Kazuhiro

  The Kitasato Institute, Center for Basic Research

• Ogawa Yasuyuki

  Center For Basic Research The Kitasato Institute

• FUNASAKA Setsuo

  Center for Basic Research, The Kitasato Institute

• YANAI Toshiharu

  Center for Basic Research, The Kitasato Institute (TCI)

• OOHASHI Yoshiaki

  Center for Basic Research, The Kitasato Institute

• KURODA Kiichi

  Department of Industrial Chemistry, Faculty of Engineering, Tokyo University of Science

• Kaneko Nobuya

  Center For Basic Research The Kitasato Institute

• Shintou Taichi

  Center For Basic Research The Kitasato Institute

• NAGAO Hitoshi

  Center for Basic Research, The Kitasato Institute

• Oohashi Yoshiaki

  The Kitasato Institute Center For Basic Research

• Fukumoto K

  The Kitasato Institute Center For Basic Research

• NAKAGAWA Takashi

  Center for Basic Research, The Kitasato Institute

• Hayashi Yujiro

  Department Of Chemistry Faculty Of Science The University Of Tokyo

• Nakagawa Takashi

  Center For Basic Research The Kitasato Institute

• Nakagawa T

  Osaka Univ. Osaka

• Mukaiyama Teruaki

  Center For Basic Research The Kitasato Institute

• Aoki Hidenori

  Center For Basic Research The Kitasato Institute

• IKEGAI Kazuhiro

  Center for Basic Research, The Kitasato Institute

• Takuwa Tomofumi

  Center For Basic Research The Kitasato Institute

• Kobashi Yohei

  Center For Basic Research The Kitasato Institute

• Funasaka Setsuo

  Center For Basic Research The Kitasato Institute

• Kawano Yoshikazu

  Otsuka Pharmaceutical Co. Ltd.

• MASUTANI Kouta

  Center for Basic Research, The Kitasato Institute

• MINOWA Tomofumi

  Center for Basic Research, The Kitasato Institute

• Masutani Kouta

  Center For Basic Research The Kitasato Institute

• Masutani K

  Kitasato Inst. Tokyo

• AOKI Hidenori

  Center for Basic Research, The Kitasato Institute

• MARUYAMA Yuji

  Department of Thoracic and Cardiovascular Surgery, Chiba-Hokusoh Hospital, Nippon Medical School

• Mukaiyama Teruaki

  Center For Basic Research The Kitasato Institute (tci)

• SAKURAI Naoto

  Center for Basic Research, The Kitasato Institute

• Sakurai Naoto

  Center For Basic Research The Kitasato Institute

• PLUEMPANUPAT Wanchai

  The Kitasato Institute, Center for Basic Research

• Matsuo Jun-ichi

  Center For Basic Research The Kitasato Institute

• Mandai Hiroki

  Center For Basic Research The Kitasato Institute (tci)

• Fujisawa H

  Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo

• Maruyama Yuji

  Department Of Neuropsychopharmacology (tsumura) Gunma University School Of Medicine

• Hagiwara Yoshiaki

  福島県立医科大学 医学部基礎病理学講座

• Hagiwara Y

  Center For Basic Research The Kitasato Institute

• Hagiwara Yoshiaki

  Center For Basic Research The Kitasato Institute

• NAGATA Yuzo

  Center for Basic Research, The Kitasato Institute (TCI)

• TOZAWA Takashi

  Department of Applied Chemistry, Faculty of Science, Science University of Tokyo

• Tozawa Takashi

  Center For Basic Research The Kitasato Institute (tci)

• Hagiwara Yoshiaki

  Ibl

• MUKAIYAMA Teruaki

  Kitasato Institute for Life Sciences, Kitasato University

• Mukaiyama Teruaki

  Center For Basic Research Kitasato University

• MICHIDA Makoto

  Process Technology Research Laboratories, Daiichi Sankyo Co., Ltd.

• Matsuo J

  Kitasato Inst. Tokyo

• Michida Makoto

  Process Technology Research Laboratories Daiichi Sankyo Co. Ltd.

• Michida Makoto

  Center For Basic Research The Kitasato Institute

• KATO Koji

  Center for Basic Research, The Kitasato Institute

• ONISHI Jim

  Center for Basic Research, The kitasato Institute

• Onishi Jim

  Center For Basic Research The Kitasato Institute

• HASHIHAYATA Takashi

  Center for Basic Research, The Kitasato Institute (TCI)

• Shintou T

  Kitasato Inst. Tokyo

• Yamanaka Hiroyuki

  Center For Basic Research Kitasato Institute

• Mukaiyama Teruaki

  Kitasato Institute For Life Sciences Kitasato University

• KIKUCHI Wataru

  Center for Basic Research, Kitasato Institute

• Hashihayata T

  Center For Basic Research The Kitasato Institute (tci)

• Kikuchi Wataru

  Center For Basic Research Kitasato Institute

• Pluempanupat Wanchai

  Center For Basic Research The Kitasato Institute

• Kato Koji

  Center For Basic Research The Kitasato Institute

• Mukaiyama Teruaki

  Kitasato Inst. For Life Sciences Kitasato Univ.

• Michida Makoto

  Center For Basic Res. The Kitasato Inst.

• JONA Hideki

  Banyu Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd.

• Jona H

  Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo

• Jona H

  Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.

• Yamane Keiko

  The Kitasato Institute Center For Basic Research

• Takeuchi K

  Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo

• NAGATA Yuzo

  The Kitasato Institute, Center for Basic Research

• Ikegai K

  The Kitasato Institute Center For Basic Research Tci

• Takuwa Tomofumi

  Center For Basic Research The Kitasato Institute 6-15-5 (tci)

• PLUEMPANUPAT Wanchai

  Center for Basic Research, The Kitasato Institute

• AOKI Hidenori

  The Kitasato Institute, Center for Basic Research

• MASUTANI Kouta

  The Kitasato Institute, Center for Basic Research

• KOBASHI Yohei

  Center for Basic Research, The Kitasato Institute (TCI)

• Kobashi Yohei

  Center For Basic Research The Kitasato Institute (tci)

• CHIBA Hiroyuki

  Center for Basic Research, Kitasato Institute

• Chiba H

  Center For Basic Research Kitasato Institute

• Yamanaka Hiroki

  Department Of Chemistry And Materials Technology Kyoto Institute Of Technology

• KANEKO Nobuya

  Center for Basic Research, The Kitasato Institute

• Kawana Asahi

  Center For Basic Research Kitasato Institute

• MANDAI Hiroki

  Center for Basic Research, The Kitasato Institute (TCI)

• Shintou Taichi

  Center For Basic Research The Kitasato Institute (tci)

• Imachi S

  Center For Basic Research The Kitasato Institute 6-15-5 (tci)

• TAKEUCHI Kazuya

  Center for Basic Research, The Kitasato Institute (TCI)

• JONA Hideki

  Center for Basic Research, The Kitasato Institute (TCI)

• YAMANAKA Hiroyuki

  Center for Basic Research, Kitasato Institute

• YAMABE Hokuto

  Center for Basic Research, The Kitasato Institute

• FUKUMOTO Kentaro

  Center for Basic Research, The Kitasato Institute

• Fukumoto Kentaro

  Center For Basic Research The Kitasato Institute

• YAMANE Keiko

  Center for Basic Research, The Kitasato Institute 6-15-5 (TCI)

• IMACHI Shouhei

  Center for Basic Research, The Kitasato Institute 6-15-5 (TCI)

• Yamanaka Hiroyuki

  Center For Basic Research The Kitasato Institute

• Yamabe Hokuto

  Center For Basic Research The Kitasato Institute

• MUKAIYAMA Teruaki

  The Kitasato Institute, Center for Basic Research

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著作論文

• Cyanation of Alcohols with Diethyl Cyanophosphonate and 2,6-Dimethyl-1,4-benzoquinone by a New Type of Oxidation-Reduction Condensation
• Preparation of Nitriles from Primary Alcohols by a New Type of Oxidation-reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Diethyl Cyanophosphonate
• An Efficient Method for the Preparation of N-Alkylamides from Alkyl Diphenylphosphinites and Amides by Using Methyl Acrylate
• A New Method for the Preparation of Nitrogen-containing Cyclic Compounds from p-Nitrobenzenesulfonamide and Alkyl Bis(diphenylphosphinite)s by Oxidation-Reduction Condensation Using 1-Azidoadamantane
• Lewis Base-Catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Carbonyl Compounds
• The Product-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones
• Ammonium Carboxylate-catalyzed [2,3]-Witting Rearrangement of Silyl Enolates Generated from α-Allyloxy Esters
• Ammonium Phenoxides-catalyzed syn-Selective Aldol Reaction Between an Aldehyde and an Trimethylsilyl Enolate
• Lewis Base-catalyzed [2, 3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones
• N-Arylation of Pyridin-2(1H)-ones with Pentavalent Organobismuth Reagents under Copper-Free Conditions
• Stereoselective Carbon-Carbon Bond Forming Reactions between Various Chiral Alkyl Aryl Carbinols and Triethyl Methanetricarboxylate by Oxidation-Reduction Condensation Using Alkyl Diphenylphosphinites
• Diastereo- and Enantioselective Tandem Michael Addition and Lactonization between Silyl Enolates and α,β-Unsaturated Ketones Catalyzed by a Chiral Quaternary Ammonium Phenoxide
• Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Chiral Quaternary Ammonium Phenoxide-catalyzed Tandem Michael Addition and Lactonization
• A Convenient Method for the Synthesis of Carboxamides and Thioesters by Using Tetrakis(2-methylimidazol-1-yl)silane
• An Efficient Method for the Preparation of Carboxamides by Dehydration Condensation Using Tetrakis(1,1,1,3,3,3-hexafluoro-2-propoxy)silane
• An Effective Method for the Synthesis of Carboxamides by Using Tetrakis(pyridine-2-yloxy)silane as a Mild Coupling Reagent
• A Convenient Method for Preparations of 1-Acylimidazoles and Carboxamides by Using Novel Imidazolylsilane Derivatives
• Stereoselective Synthesis of trans-3, 4-Dihydropyran-2-ones by Phenoxide ion-catalyzed Tandem Michael Addition and Lactonization
• An Efficient Synthesis of 3, 4-Dihydropyran-2-one Derivatives by Lewis Base-catalyzed Tandem Michael Addition and Lactonization
• Lithium Alkoxide-promoted Michael Reaction between Silyl Enolates and α, β-Unsaturated Carbonyl Compounds
• A Convenient Method for the Synthesis of (Z)-α-Fluoroacrylates : Lewis Base-catalyzed Carbonyl Fluoroolefination Using Fluoro(trimethylsilyl)ketene Ethyl Trimethylsilyl Acetal
• Copper(II)-catalyzed O-Phenylation of Alcohols with Organobismuth(V) Reagents : A Convenient Method for the Synthesis of Simple tert-Alkyl Phenyl Ethers
• New Preparative Method of Aryl Tosylates by Using Organobismuth Reagents
• Direct α-Oxytosylation of Ketones by Using Pentavalent Organobismuth Reagents
• Stereospecific C-S Bond Formation from Chiral Tertiary Alcohols by Quinone-Mediated Oxidation-Reduction Condensation Using Alkyl Diphenylphosphinites and Its Application to the Synthesis of a Chiral Tertiary Thiol
• Preparation of tert-Alkyl Aryl Sulfides from tert-Alcohols via Quinone mediated Oxidation-Reduction Condensation between tert-Alkyl Diphenylphosphinites and 2-Sulfanyl-1, 3-benzothiazole
• New methods for carbon–nitrogen, carbon–sulfur, and carbon–carbon bond formations by quinone-mediated oxidation–reduction condensation using alkyl diphenylphosphinites
• A Convenient Method for the Lewis Base-catalyzed Synthesis of α,β-Unsaturated Carboxylic Esters Using Trimethylsilylketene Ethyl Trimethylsilyl Acetal and Carbonyl Compounds
• Diastereoselective Cyanomethylation of Chiral N-(tert-Butylsulfinyl)imines Promoted by Lewis Bases
• Lewis Base Catalyzed 1,3-Dithiane Addition to Carbonyl Compounds Using 2-Trimethylsilyl-1,3-dithiane
• Trimethylsilyl Triflate Mediated New Carbon-Carbon Bond Forming Reactions between Benzyl Diphenylphosphinates and Organosilicon Compounds
• Highly Efficient Method for the Synthesis of Carboxamides from Carboxylic Acids and Amines Using Pyridine-3-sulfonyl Chloride (3-PSC)
• Highly Efficient Method for the Synthesis of Carboxamides from Carboxylic Acids and Amines Using Benzenesulfonic Anhydride (BSA)
• Pyridine-3-carboxylic Anhydride (3-PCA) : A Versatile, Practical, and Inexpensive Reagent for Condensation Reaction between Carboxylic Acids and Alcohols
• Catalytic and Stereoselective Glycosylation with Glucosyl Thioformimidates
• Efficient Method for Dehydration Condensation Using Pyridine-3-carboxylic Anhydride (3-PCA) : Synthesis of Carboxamides from Nearly Equimolar Amounts of Carboxylic Acids and Amines
• Lewis Base-catalyzed Cyanomethylation of Aldimines with Trimethylsilylacetonitrile
• Highly Stereoselective Samarium(II) Iodide-Mediated Aldol Reactions of Acylaziridines with Aldehydes
• Highly trans-Selective Synthesis of β-Lactams by Tandem Phenoxide Anion-catalyzed Mannich-type Addition and Cyclization
• Efficient Method for the Lactonization of ω-Hydroxycarboxylic Acids with Di-2-thienyl Carbonate by the Promotion of Catalytic Amounts of DMAP and Hf(OTf)_4
• Enantioselective Synthesis of C11-C17 Segment of Mycinolide IV Using Samarium(II) Iodide-mediated Aldol Reaction
• A Facile One-Pot Benzylation of Sodium Enolates Using Trifluoromethanesulfonic Anhydride and Diphenyl Sulfoxide
• Lithium Acetate-catalyzed Crossed Aldol Reaction between Aldehydes and Trimethylsilyl Enolates Generated from Other Aldehydes
• Lewis Base-catalyzed Diastereoselective Strecker-type Reaction between Trimethylsilyl Cyanide and Chiral Sulfinimines
• Lewis Base-catalyzed Diastereoselective Mannich-type Reaction between Ketene Silyl Acetals and Chiral Sulfinimines
• Lewis Base-catalyzed Trifluoromethylation of Aldimines with (Trifluoromethyl)trimethylsilane
• Stereoselective Synthesis of δ-Amino-β'-Hydroxy-β, γ-Unsaturated Esters by the Samarium(II) Iodide-mediated Aldol Reaction of Aldehydes with γ, δ-Aziridiny-α, β-Unsaturated Esters
• Conversion of Alcohols to Alkyl Aryl Sulfides by a New Type of Oxidation-Reduction Condensation Using Phenyl Diphenylphosphinite
• Stereospecific Synthesis of sec- and tert-Alkyl Azides from Alcohols and Trimethylsilyl Azide by a New Type of Oxidation-Reduction Condensation Using Phenyl Diphenylphosphinite and Trimethylsilylmethyl Azide
• Stereospecific Synthesis of Alkyl Aryl Sulfides from Alcohols and 2-Sulfanylbenzothiazole Using Aryl Diphenylphosphinite and Azide Compounds by a New Type of Oxidation-Reduction Condensation
• Preparation of Alkyl Aryl Sulfides from Alcohols and 2-Sulfanylbenzothiazole by a New Type of Oxidation-Reduction Condensation Using Aryl Diphenylphosphinite and Benzoquinone Derivatives
• Preparation of tert-Alkyl Azides from Tertiary Alcohols by Way of Benzoquinone-mediated Oxidation-Reduction Condensation
• A New Method for the Synthesis of β-Amino-β'-Hydroxy Ketones by the Samarium(II) Iodide-mediated Aldol Reaction of Aldehydes with Aryl or Alkyl Aziridinyl Ketones
• Stereoselective Synthesis of 19-Hydroxytaxoid Using Intramolecular Pinacol Coupling Reaction
• A Facile One-pot Benzylation of Sodium Enolates Using Trifluoromethansulfonic Anhydride and Diphenyl Sulfoxide
• 6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations
• Lewis Base-Catalyzed Perfluoroalkylation of Carbonyl Compounds and Imines with (Perfluoroalkyl)trimethylsilane
• An Efficient Method for the Preparation of Chiral Mosher's Acid Analogues
• A Convenient Method for the Preparation of Alkyl Aryl Sulfides from Alcohols and (Chloromethylene)dimethylammonium Chloride
• Lewis Base-catalyzed Cyanomethylation of Carbonyl Compounds with (Trimethylsilyl)acetonitrile
• Asymmetric Trifluoromethylation of Ketones with (Trifluoromethyl)trimethylsilane Catalyzed by Chiral Quaternary Ammonium Phenoxides
• Effective Synthesis of 5-Substituted Butenolide Derivatives by Using Cinchonidine-derived Quaternary Ammonium Phenoxide Catalyst
• Efficient synthesis of substituted 3-amino-3,4-dihydropyran-2-ones diastereo and enantioselective tandem Michael addition and lactonization between α,β-unsaturated ketones and glycine-derived silyl enolates using a chiral quaternary ammonium phenoxide
• Diastereo- and Enantioselective Synthesis of 3-Amino-3,4-dihydropyran-2-ones by Tandem Michael Addition and Lactonization Using a Chiral Quaternary Ammonium Phenoxide
• Diastereo- and Enantioselective Tandem Michael Addition and Lactonization Catalyzed by Chiral Quaternary Ammonium Phenoxide : Stereoselective Synthesis of the Two Enantiomers by Using a Single Chiral Source
• A New Method for the Preparation of Alkyl Aryl Sulfides from Alcohols via Alkoxydiphenylphosphines by Oxidation-Reduction Condensation
• Convergent Total Syntheses of Oligosaccharides by One-Pot Sequential Stereoselective Glycosylations
• A Convenient Method for the Synthesis of 2-Arylaziridines from Styrene Derivatives via 2-Arylethenyl(diphenyl)sulfonium Salts
• Selective Synthesis of Isocyanides from Secondary Alcohols by a New Type of Oxidation-Reduction Condensation
• Facile One-pot Syntheses of Amidines and Enamines from Oximes via Beckmann Rearrangement Using Trifluoromethansulfonic Anhydride
• Lewis Base-catalyzed Strecker-type Reaction between Trimethylsilyl Cyanide and N-Tosylimines in Water-containing DMF
• One-pot Synthesis of β-Lactams from Aldimines and Ketene Silyl Acetals by Tandem Lewis Base-catalyzed Mannich-type Addition and Cyclization
• Efficient Method for the Esterification of Carboxylic Acids with Alcohols Using Di-2-thienyl Carbonate Promoted by Catalytic Amounts of DMAP and Hf(OTf)_4
• A New Method for the Lactonization of ω-Hydroxy Carboxylic Acids with Di-2-thienyl Carbonate by the Promotion of DMAP and Iodine
• Efficient Method for the Esterification of Carboxylic Acids with Alcohols Using Di-2-thienyl Carbonate Promoted by DMAP and Iodine
• A New Method for the Esterification of Carboxylic Acids with Various Alcohols by Using Di-2-thienyl Carbonate, a New Coupling Reagent
• Copper(II)-catalyzed O-Phenylation of Tertiary Alcohols with Organobismuth(V) Reagents
• A New Method for α-Selective Glycosylation Using a Donor, Glycosyl Methyldiphenylphosphonium Iodide, without Any Assistance of Acid Promoters
• Lewis Base-Catalyzed Michael Reactions between Trimethylsilyl Enolate and α, β-Unsaturated Carbonyl Compounds
• Lithium Acetate-catalyzed Trifluoromethylation of Carbonyl Compounds with (Trifluoromethyl)trimethylsilane
• Lewis Base-catalyzed anti-Selective Mannich-type Reaction between Trimethylsilyl Enolates and Aldimines
• Product-catalyzed Mannich-type Reaction between Trimethylsilyl Enolates and N-Tosylaldimines
• Lithium Acetate-Catalyzed Aldol Reaction between Aldehyde and Trimethylsilyl Enolate in Anhydrous or Water-Containing N, N-Dimethylformamide
• Lithium Acetate-catalyzed Michael Reaction between Trimethylsilyl Enolate and α, β-Unsaturated Carbonyl Compound
• Diastereoselective Trifluoromethylation of Chiral N-(Tolylsulfinyl)imines in the Presence of Lewis Bases
• Enantioselective Trifluoromethylation of Ketones with (Trifluoromethyl)trimethylsilane Catalyzed by Chiral Quaternary Ammonium Phenoxides
• A Versatile, Practical, and Inexpensive Reagent, Pyridine-3-carboxylic Anhydride (3-PCA), for Condensation Reactions
• Alkyl Phosphinites : Versatile Synthetic Intermediates for Dehydration Condensation Reactions
• 6-Nitro-2-benzothiazolyl α-Mannoside : A Highly Efficient Mannosyl Donor in Constructing β-Man(1→4)GlcN Linkage and Its Application to the Synthesis of the Pentasaccharide Core of N-Glycans
• Synthesis of N-Aryl Pyridin-2-ones via Ligand Coupling Reactions Using Pentavalent Organobismuth Reagents
• An Efficient Method for Alkylation of Alcohols with Alkyl P, P-diphenyl-N-(methanesulfonyl)phosphinimidates
• Efficient Method for the Preparation of Primary, Inverted Secondary and Tertiary Alkyl Carboxylates from Alcohols and Carboxylic Acids by a New Type of Oxidation-Reduction Condensation Using Simple 1,4-Benzoquinone
• Efficient Method for the Preparation of Carboxylic Acid Alkyl Esters or Alkyl Phenyl Ethers by a New-Type of Oxidation-Reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Alkoxydiphenylphosphines
• New One-pot Cross-coupling Reaction between Grignard Reagents and Alkoxymethyldiphenylphosphonium Iodides in situ-Formed from Alcohols, Chlorodiphenylphosphine and Iodomethane
• Efficient Method for the Preparation of Inverted Alkyl Carboxylates and Phenyl Carboxylates via Oxidation-Reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone or Simple 1, 4-Benzoquinone
• Efficient and Concise Synthesis of βMan1-4GlcN Linkage of Pentasaccharide Core by Using 6-Nitro-2-benzothiazolyl α-Mannoside
• Glycosyl Phosphonium Halide as a Reactive Intermediate in Highly α-Selective Glycosylation
• Highly α-Selective Synthesis of Disaccharide Using Glycosyl Bromide by the Promotion of Phosphine Oxide
• A Convenient Method for the Synthesis of α-Imidostyrenes from Styrenes and Imides via Diphenylstyrylsulfonium Salts
• Stereoselective Crossed Aldol Reaction via Boron Enolates Generated from α-Iodo Ketones and 9-Borabicyclo[3. 3. 1]nonane
• Self-promoted Aldol Reaction between Aldehyde Having Lewis Base Moiety and Trimethylsilyl Enolate
• Lithium Acetate Catalyzed Aldol Reaction between Aldehyde and Trimethylsilyl Enolate in a Dimethylformamide-H_2O Solvent
• N-Alkylation of Phthalimide, Carboxamide, and Sulfonamides By Oxdation-Reduction Condensation Using Di-tert-butyl-1, 4-benzoquinone and Alkyl Diphenylphosphinite

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