Regio-and Stereo-defined Synthesis of Organosilicon Compounds via Rearrangement of Silyl Group
スポンサーリンク
概要
- 論文の詳細を見る
- 1992-08-05
著者
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Kuwajima Isao
Department Of Chemistry Tokyo Institute Of Technology
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MARUMOTO Shinji
Department of Chemistry, Tokyo Institute of Technology
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Marumoto Shinji
Department Of Chemistry Tokyo Institute Of Technology
関連論文
- Preparation and Properties of Highly Electron-accepting Poly(pyrimidine-2,5-diyl)
- Construction of N-Acylated 4-Piperidones via Selective Carbon-Nitrogen and Carbon-Carbon Bond Formation
- Remarkable Stereochemical Features of Ene Reaction of 2-(Alkylthio)crotyl Silyl Ethers. Proposal of a Six-Membered Chair-like Transition State
- New Aspects of Vinylsulfide Chemistry
- Diastereoselective Conjugate Addition for Construction of Taxane Precursors
- Synthesis of C-Aromatic Taxinine Derivatives
- Regio-and Stereo-defined Synthesis of Organosilicon Compounds via Rearrangement of Silyl Group
- New Aspects of Vinylsulfide Chemistry
- Reactions of 2,3,5-tri-O-benzoyl-D-ribofuranosyl acetate with enol silyl ethers catalyzed by tin(IV) chloride. Regiochemical features.
- Specific generation of lithiated 3-trimethylsiloxy-1,2-propadiene derivatives from 1-(trimethylsilyl)propargyl alcohols.
- Reactions of 2-chloroacyltrimethylsilanes with Grignard reagents. Preparation of 3-(trimethylsilyl)-2-alkanones and 2-(trimethylsilyl)-1-alkanols.
- Oxidation of olefins into .ALPHA.-phenylseleno carbonyl compounds. Highly regioselective anti-Markownikoff type oxidation of allylic alcohol derivatives.
- One-step oxidation of olefins into .ALPHA.-phenylseleno carbonyl compounds.
- Silylation of relatively acidic compounds with alkyl trimethylsilylacetates.
- Conversion of carbon-sulfur linkages into carbon-silicon ones via reductive silylation. Preparation of silyl enol ethers of acyltrimethylsilanes.
- A remarkable solvent effect on the reductive silylation of carboxylic esters. Preparation of 1,1-bis(trimethylsilyl)-1-alkanols.