Chiral 1,3-Oxathiane from (+)-Pulegone: Hexahydro-4,4,7-trimethyl-4H-1,3-benzoxathiin-Reference-Cited by-同舟云学术

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Chiral 1,3-Oxathiane from (+)-Pulegone: Hexahydro-4,4,7-trimethyl-4H-1,3-benzoxathiin

Published:2003-04-28 Issue: Volume: Page:215-215
ISSN:
Container-title:Organic Syntheses
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Author:

Eliel Ernest L.¹,Lynch Joseph E.¹,Kume Fumitaka¹,Frye Stephen V.¹

Affiliation:

1. University of North Carolina; W. R. Kenan, Jr. Laboratories; Department of Chemistry; Chapel Hill NC 27514

Publisher

John Wiley & Sons, Inc.

Reference7 articles.

1. Convenient synthesis of (S)-(-)-pulegone from (-)-citronellol

2. 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.

3. Whitesell , J. K.

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

5. Asymmetric reactions based on 1,3-oxathianes3̄

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