The configurations of (−)-2,3,3-trimethyl-2-hydroxybutanoic acid, Me3CC(Me)(OH)CO2H, (−)-3,3,4-trimethyl-3-hydroxy-1-pentyne and (−)-3--butyl-3-methyl-1-chloroallene-Reference-Cited by-同舟云学术

The configurations of (−)-2,3,3-trimethyl-2-hydroxybutanoic acid, Me3CC(Me)(OH)CO2H, (−)-3,3,4-trimethyl-3-hydroxy-1-pentyne and (−)-3--butyl-3-methyl-1-chloroallene

Published:1987-01 Issue:41 Volume:28 Page:4813-4816
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Eliel Ernest L.,Lynch Joseph E.,Kenan William R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

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2. Asymmetric synthesis of nearly optically pure atrolactic acid methyl ether

3. CHIRAL 1,3-OXATHIANE FROM (+)-PULEGONE: HEXAHYDRO-4,4,7-TRIMETHYL-4H-1,3-BENZOXATHIIN

4. Asymmetric synthesis of ()-(+)-ethylmethyl--propylcarbinol in high enantiomeric purity. A 1,3-oxathiane derived from (+)-pulegone as chiral adjuvant

5. Asymmetric syntheses based on 1,3-oxathianes. 2. Synthesis of chiral tertiary .alpha.-hydroxy aldehydes, .alpha.-hydroxy acids, glycols [R1R2C(OH)CH2OH], and carbinols [R1R2C(OH)Me] in high enantiomeric purity.

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