Iwama T | Gifu Pharmaceutical University
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概要
関連著者
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Iwama Tetsuo
Gifu Pharmaceutical University
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Iwama T
Gifu Pharmaceutical University
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Iwamura T
Gifu Pharmaceutical Univ. Gifu Jpn
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Kataoka T
Gifu Pharmaceutical Univ. Gifu Jpn
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渡辺 真一
岐阜薬科大学
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清水 博
東大
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清水 博
東大・薬
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KATAOKA Tadashi
Gifu Pharmaceutical University
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Tanabe Genzoh
School Of Pharmacy Kinki University
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Muraoka Osamu
Department Of Pharmacology Osaka University School Of Medicine
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Muraoka Osamu
School Of Pharmacy Kinki Univ.
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Muraoka Osamu
School Of Pharmacy Kinki University
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Tanabe G
Faculty Of Pharmaceutical Sciences Kinki University
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Matsumoto H
Yamanouchi Pharmaceutical Co. Ltd. Ibaraki Jpn
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清水 博
東京大学・薬学部
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清水 博
東大薬
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Iwamura Tatsunori
Gifu Pharmaceutical University
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TSUJIYAMA Shin-ichiro
Gifu Pharmaceutical University
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KANEMATSU Kiyoko
Gifu Pharmaceutical University
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WATANABE Shin-ichi
Gifu Pharmaceutical University
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Iwamura Tatsunori
Gifu Pharmaceutical Univ. Gifu Jpn
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MATSUMOTO Harutoshi
Gifu Pharmaceutical University
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SHIMIZU Hiroshi
Gifu Pharmaceutical University
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KINOSHITA Hironori
Gifu Pharmaceutical University
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TSURUKAMI Yasuo
Gifu Pharmaceutical University
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ITO Taizo
Gifu Pharmaceutical University
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Tsujiyama Shinichiro
Gifu Pharmaceutical University
著作論文
- Dimethyl Sulfide-Boron Trihalide-Mediated Reactions of α, β-Unsaturated Ketones with Aldehydes : One-pot Synthesis of Baylis Hillman Adducts and α-Halomethyl Enones
- Self-assisted Tandem Michael-aldol Reactions of α, β-Unsaturated Ketones with Aldehydesl.
- The First Aryne Evolution from the Reactions of Selenonium Salts with Aryllithiums.
- A Novel Stereoselective Preparation of Various Vinyl Sulfide Derivatives Using β-Alkylthioalkenylselenonium Salts.
- A Convenient Synthesis of α-Halomethylene Adols or β-Halo-α-(hydroxyalkyl)acrylates Using the Chalcogeno-Baylis-Hillman Reaction. Α
- First Isolation of Selenabenzenes Stabilized by Two Electron-withdrawing Groups at the 2- and 6-Positions.
- Reactions of 1,2-Thiazetidine 1,1-Dioxides with Organometallics : β-Elimination and N-S Bond Cleavage.
- A New Synthesis of α-Amino Acid Thioesters by Pummerer Reaction of 3-Substituted-4-sulfinyl-β-sultams.
- Reactions of a β-Sultam Ring with Lewis Acids via the C-S Bond Cleavage.
- The Enantioselective Chalcogeno-Baylis-Hillman Reaction Using a Chiral Hydroxy Chalcogenide-TiCl_4 Complex.
- The Chalcogeno-Baylis-Hillman Reaction of α, β-Unsaturated Thioester : A New Approach to α-Methylene-β-hydroxy Carboxylic Acid Derivatives.
- A New Entry to Enantioselective Synthesis of α-Methylene-β-hydroxy Ketones by the Chalcogeno-Baylis-Hillman Reaction.
- A New Entry to Enantioselective Synthesis of α-Nethylene-β-hydroxy Ketones by the Chalcogeno-Baylis-Hillman Reaciton
- The Chalcogeno-Baylis-Hillman Reaction : The First Examples Catalyzed by Chalcogenides in the Presence of Lewis Acids.
- The Enantioselective Chalcogeno - Baylis - Hillman Reaction Using a Chiral Hydroxy Chalcogenide - TiCl_4 Complex
- Photochemical[3+2]Cycloaddition of 2'-Vinyl-2H-1,4-benzothiazine-3(4H)-one-2-spirocyclopropanes Catalyzed by Diphenyl Dichalcogenides.
- Photochemical [3+2] Cycloaddition of 2'-Vinyl-2H-1,4-benzothiazin-3(4H)-one-2-spirocyclopropanes Catalyzed by Diphenyl Dichalcogenides
- Generation and Reactions of Butadienylthionium Ions from 2-Vinylcyclopropyl Sulfoxides under Pummerer Conditions
- The Chalcogeno-Baylis-Hillman Reaction : A New Preparation of Allylic Alcohols from Aldehydes and Electron-deficient Alkenes.