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ChemInform Abstract: α‐Chelation Controlled Nucleophilic Addition to Chiral αβ‐Dialkoxy Carbonyl Compounds. Diastereoselective Preparation of L‐xylo and L‐lyxo Triols.

Hideo Iida, Naoki Yamazaki, C. KIBAYASHI

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Abstract

Abstract The Grignard reagents (II) react with the L‐threose derivative (I) to form the xylo alcohols (III) as the main products, together with the lyxo alcohols (IV).

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What this paper is about

Abstract The Grignard reagents (II) react with the L‐threose derivative (I) to form the xylo alcohols (III) as the main products, together with the lyxo alcohols (IV).

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Available abstract

Abstract The Grignard reagents (II) react with the L‐threose derivative (I) to form the xylo alcohols (III) as the main products, together with the lyxo alcohols (IV).

Key concepts: Chemistry, Reagent, Chelation, Nucleophilic addition, Derivative (finance), Nucleophile, Grignard reagent, Organic chemistry

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ChemInform Abstract: α‐Chelation Controlled Nucleophilic Addition to Chiral αβ‐Dialkoxy Carbonyl Compounds. Diastereoselective Preparation of L‐xylo and L‐lyxo Triols. — Research Paper | ScholarLens