PREPARATION AND REACTION OF NOVEL OXYGEN ESTER ENOLATES, 2,REACTION OF GLYCOLATE WITH ALDEHYDES USING DIALKYLBORYL TRIFLATE
スポンサーリンク
概要
- 論文の詳細を見る
The introduction of an oxygen atom substituent into the α-position of oxygen ester made it possible to generate corresponding boron enolates by the use of dialkylbouyl trifluoromethanesulfonate. These novel boron enolates of oxygen ester proceeded aldol reaction with various aldehydes in high yield and with excellent syn diastereoselectivity to provide glyceric acid derivatives.
- 1989-03-25
著者
関連論文
- Photochemical Synthesis of Azepinoindoles and Azocinoindoles from N-Chloroacetylindolylethylamines, and a Mechanistic Study based on the Correlation between Quantum Yields and Calculated Frontier Electron Densities of Indole Radicals
- Flash Photolysis of Allyl Phenyl Ethers
- Mechanism of Photocyclization of N-Chloroacetyl-m-tyramine A Flash Photolysis Study
- Photo-rearrangements of Methyl Indole-1-acetate, Indole-1-acetamide and Methyl Indoline-1-acetate
- Photo-induced Friedel-Crafts Reactions. IV. Indoleacetic Acids
- Photo-induced Friedel-Crafts Reaction. II
- Optical Resolution of (±)-2-[4-(2-Oxocyclohexylidenemethyl)phenyl]propionic Acid
- Opitical Resolution and Determination of Absolute Configuration of 2-(2-Isopropylindan-5-yl) propionic Acid
- Bischler-Napieralski Reactions of N-(2-Indolylethyl) acetamide
- PREPARATION AND REACTION OF NOVEL OXYGEN ESTER ENOLATES, 2,REACTION OF GLYCOLATE WITH ALDEHYDES USING DIALKYLBORYL TRIFLATE
- PREPARATION AND REACTION OF NOVEL OXYGEN ESTER ENOLATES, 1, : REACTION OF THIOGLYCOLATE WITH ALDEHYDES USING DIALKYLBORYL TRIFLATE