Highly diastereoselective reduction and alkylation of (1R,2S)-trans-2-phenylcyclohexanol phenylglyoxylate and pyruvate using hindered hydrides and alkyl aluminates-Reference-Cited by-同舟云学术

Highly diastereoselective reduction and alkylation of (1R,2S)-trans-2-phenylcyclohexanol phenylglyoxylate and pyruvate using hindered hydrides and alkyl aluminates

Published:1999-09 Issue:38 Volume:40 Page:6919-6922
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Boireau Gérard,Deberly Alain,Loupy André,Monteux Daphné

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. (R)-(+)- and (S)-(-)-5-Ethyl-5-methyl-1,3-dioxolane-2,4-dione reagents for the direct preparation of .alpha.-hydroxy-.alpha.-methylbutyrate esters: assignment of the absolute configuration of the .alpha.-acetoxy-.alpha.-methylbutyrate ester side chain of quassimarin via total synthesis

2. Proline Benzyl Ester as Chiral Auxiliary in Barbier-Type Reactions in Aqueous Solution

3. Highly diastereoselective reduction of (−) menthylphenylglyoxalate and (−) menthylpyruvate using new hindered lithiumtrialkoxyaluminohydrides

4. Hauts rendements optiques obtenus dans la synthese d′α-alkylα-hydroxyesters par reaction d'alkoxytrialkylaluminates encombres avec le phenylglyoxalate de menthyle.

5. Synthese D'α-hydroxy acides optiquement actifs

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