橋本 俊一 | Faculty Of Pharmaceutical Sciences University Of Tokyo
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概要
関連著者
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橋本 俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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橋本 俊一
Faculty Of Pharmaceutical Sciences Hokkaido University
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古賀 憲司
Faculty of Pharmaceutical Sciences, University of Tokyo
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Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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山田 俊一
Faculty of Pharmaceutical Sciences, University of Tokyo
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池上 四郎
帝京大学薬学部
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橋本 俊一
北大院薬
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山田 俊一
東京大学
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山田 俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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池上 四郎
Faculty of Pharmaceutical Sciences, Teikyo University
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池上 四郎
Faculty Of Pharmaceutical Sciences Teikyo University
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池上 四郎
帝京大 薬
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中島 誠
Faculty Of Pharmaceutical Sciences University Of Tokyo
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中島 誠
北海道大学大学院薬学研究科
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佐野 愛
Faculty of Pharmaceutical Sciences, Hokkaido University
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梅尾 和寛
Faculty of Pharmaceutical Sciences, Hokkaido University
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本田 雄
帝京大学薬学部
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本田 雄
Faculty of Pharmaceutical Sciences, Teikyo University
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中島 正晴
県立食品総合研究所
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梅尾 和寛
Faculty Of Pharmaceutical Sciences Hokkaido University
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米島 伸泰
Faculty of Pharmaceutical Sciences, University of Tokyo
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米島 伸泰
Pharmaceutical Research Laboratory Kirin Brewery Co. Ltd.
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Umeo Kazuhiro
Faculty Of Pharmaceutical Sciences Hokkaido University
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Nakajima Mitsuhiro
Minahealth Co. Ltd.
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池上 四郎
帝京大学
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佐野 愛
Faculty Of Pharmaceutical Sciences Hokkaido University
著作論文
- AN EXTREMELY MILD AND GENERAL METHOD FOR THE CONSTRUCTION OF 1,2-TRANS-β-GLYCOSIDIC LINKAGES VIA GLYCOPYRANOSYL DIETHYL PHOSPHITES WITH PARTICIPATING GROUPS AT C-2
- AN EFFICIENT CONSTRUCTION OF 1,2-TRANS-β-GLYCOSIDIC LINKAGES VIA BENZYL-PROTECTED GLYCOPYRANOSYL P, P-DIPHENYL-N-(p-TOLUENESULFONYL)-PHOSPHINIMIDATES
- Stereoselective Reactions. II. Asymmetric Synthesis of β-Substituted Aldehydes by Michael Reaction using Chiral α, β-Unsaturated Aldimines
- Stereoselective Reactions. I. A highly Efficient Asymmetric Synthesis of β-Substituted Aldehydes via 1,4-Addition of Grignard Reagents to optically Active α, β-Unsaturated Aldimines
- Stereoselective Reactions. III. A highly Efficient Method for the Asymmetric Synthesis of 2-Alkylcycloalkanones via Chiral Chelated Lithioenamines