MUKAIYAMA Teruaki | Center for Basic Research, The Kitasato Institute
スポンサーリンク
概要
関連著者
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MUKAIYAMA Teruaki
Center for Basic Research, The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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Minowa Tomofumi
Kitasato Institute For Life Sciences Kitasato University
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Mukaiyama T
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
The Kitasato Institute Center For Basic Research
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Minowa Tomofumi
Center For Basic Research The Kitasato Institute
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FUJISAWA Hidehiko
Center for Basic Research, The Kitasato Institute
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Fujisawa Hidehiko
Center For Basic Research The Kitasato Institute
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Tozawa Takashi
Center For Basic Research The Kitasato Institute
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KURODA Kiichi
Center for Basic Research, The Kitasato Institute
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Kuroda Kiichi
Center For Basic Research The Kitasato Institute
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Sato Yoshinori
Center For Basic Research The Kitasato Institute
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HAYASHI Yujiro
Department of Human and Mechanical Systems Engineering, Kanazawa Univ.
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Hayashi Yujiro
Department Of Chemistry School Of Science The University Of Tokyo
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Ogawa Yozo
Department Of Applied Chemistry Faculty Of Engineering Okayama University Of Science
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Ogawa Yasuyuki
Center For Basic Research The Kitasato Institute
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YAMANE Yoshinobu
Center for Basic Research, The Kitasato Institute
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FUNASAKA Setsuo
Center for Basic Research, The Kitasato Institute
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Funasaka Setsuo
Center For Basic Research Kitasato Institute
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KURODA Kiichi
Department of Industrial Chemistry, Faculty of Engineering, Tokyo University of Science
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Yamane Yoshinobu
Center For Basic Research The Kitasato Institute
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Hayashi Yujiro
Department Of Chemistry Faculty Of Science The University Of Tokyo
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Funasaka Setsuo
Center For Basic Res. The Kitasato Inst.
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Funasaka Setsuo
Center For Basic Research The Kitasato Institute
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MINOWA Tomofumi
Center for Basic Research, The Kitasato Institute
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MARUYAMA Yuji
Department of Thoracic and Cardiovascular Surgery, Chiba-Hokusoh Hospital, Nippon Medical School
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YANAI Tomoko
Shinnikka Environmental Engineering Co. Ltd.
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Takahashi Eiki
Kitasato Institute For Life Sciences Kitasato University
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IKEGAI Kazuhiro
Center for Basic Research, The Kitasato Institute
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Ikegai Kazuhiro
Center For Basic Research The Kitasato Institute
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SAKURAI Naoto
Center for Basic Research, The Kitasato Institute
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Sakurai Naoto
Center For Basic Research The Kitasato Institute
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KAWANO Yoshikazu
Center for Basic Research, The Kitasato Institute
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TAKAHASHI Eiki
Center for Basic Research, The Kitasato Institute (TCI)
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YANAI Toshiharu
Center for Basic Research, The Kitasato Institute (TCI)
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Kawano Yoshikazu
Center For Basic Research The Kitasato Institute
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Maruyama Yuji
Department Of Neuropsychopharmacology (tsumura) Gunma University School Of Medicine
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Hagiwara Yoshiaki
福島県立医科大学 医学部基礎病理学講座
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Hagiwara Y
Center For Basic Research The Kitasato Institute
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Hagiwara Yoshiaki
Center For Basic Research The Kitasato Institute
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MASUTANI Kouta
Center for Basic Research, The Kitasato Institute
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Masutani Kouta
Center For Basic Research The Kitasato Institute
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Masutani K
Kitasato Inst. Tokyo
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NAGATA Yuzo
Center for Basic Research, The Kitasato Institute (TCI)
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Mukaiyama Teruaki
Center For Basic Research The Kitasato Institute
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TOZAWA Takashi
Department of Applied Chemistry, Faculty of Science, Science University of Tokyo
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Tozawa Takashi
Center For Basic Research The Kitasato Institute (tci)
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Hagiwara Yoshiaki
Ibl
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Nagata Yuzo
Center For Basic Research The Kitasato Institute
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IKEGAI Kazuhiro
The Kitasato Institute, Center for Basic Research
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Mukaiyama Teruaki
Center For Basic Research Kitasato University
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Takuwa Tomofumi
Center For Basic Research The Kitasato Institute
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MICHIDA Makoto
Process Technology Research Laboratories, Daiichi Sankyo Co., Ltd.
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Matsuo Jun-ichi
Center For Basic Research The Kitasato Institute
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Michida Makoto
Process Technology Research Laboratories Daiichi Sankyo Co. Ltd.
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Michida Makoto
Center For Basic Research The Kitasato Institute
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KATO Koji
Center for Basic Research, The Kitasato Institute
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Fujisawa H
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Kato Koji
Center For Basic Research The Kitasato Institute
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Michida Makoto
Center For Basic Res. The Kitasato Inst.
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AOKI Hidenori
Center for Basic Research, The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Research The Kitasato Institute (tci)
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Aoki Hidenori
Center For Basic Research The Kitasato Institute
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PLUEMPANUPAT Wanchai
The Kitasato Institute, Center for Basic Research
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PLUEMPANUPAT Wanchai
Center for Basic Research, The Kitasato Institute
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Matsuo J
Kitasato Inst. Tokyo
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KOBASHI Yohei
Center for Basic Research, The Kitasato Institute (TCI)
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Kobashi Yohei
Center For Basic Research The Kitasato Institute
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CHIBA Hiroyuki
Center for Basic Research, Kitasato Institute
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Chiba H
Center For Basic Research Kitasato Institute
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OOHASHI Yoshiaki
Center for Basic Research, The Kitasato Institute
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FUKUMOTO Kentarou
Center for Basic Research, The Kitasato Institute
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KANEKO Nobuya
Center for Basic Research, The Kitasato Institute
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ONISHI Jim
Center for Basic Research, The kitasato Institute
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Onishi Jim
Center For Basic Research The Kitasato Institute
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HASHIHAYATA Takashi
Center for Basic Research, The Kitasato Institute (TCI)
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MANDAI Hiroki
Center for Basic Research, The Kitasato Institute (TCI)
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Kaneko Nobuya
Center For Basic Research The Kitasato Institute
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Mandai Hiroki
Center For Basic Research The Kitasato Institute (tci)
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Oohashi Yoshiaki
The Kitasato Institute Center For Basic Research
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Fukumoto K
The Kitasato Institute Center For Basic Research
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Fukumoto Kentarou
Center For Basic Research The Kitasato Institute
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Hashihayata T
Center For Basic Research The Kitasato Institute (tci)
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Pluempanupat Wanchai
Center For Basic Research The Kitasato Institute
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
- 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
- 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
- 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
- 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
- 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