A Divergent Synthesis of Essentially Enantiopure syn-and anti-Propionate Aldol Adducts Based on the Chiral 1,3,2-Oxazaborolidin-5-one-Promoted Asymmetric Aldol Reaction Followed by Diastereoselective Radical Reduction

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概要

• 論文の詳細を見る
• Chemical Society of Japanの論文
• 2001-08-15

著者

• KIYOOKA Syun-ichi

  Department of Chemistry, Faculty of Science, Kochi University

• Kiyooka Syun-ichi

  Department Of Chemistry Kouchi University

• Kiyooka Syun-ichi

  Department Of Chemistry Faculty Of Science Kochi University

• SHAHID Abuds

  Department of Chemistry, Kouchi University

• Shahid Abuds

  Department Of Chemistry Kouchi University

• Shahid Kazi

  Department of Chemistry, Kouchi University

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• Synthesis of (S)-Ketamine via [1,3]-Chirality Transfer of a Stereocenter Created by Enantioselective Aldol Reaction
• Synthesis of Chiral Crown Ethers Having Bromoarylene Moieties on Their Rim. Anomalous Behavior of Racemic Substrates in Cyclization to Crown Ethers
• A Divergent Synthesis of Essentially Enantiopure syn-and anti-Propionate Aldol Adducts Based on the Chiral 1,3,2-Oxazaborolidin-5-one-Promoted Asymmetric Aldol Reaction Followed by Diastereoselective Radical Reduction
• Photochemical decarbonylation of (.ALPHA.-arylacyl)triphenylgermane.

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