Synthesis of a New (1R)-(−)-Myrtenal-Derived Dioxadithiadodecacycle and Its Use as an Efficient Chiral Auxiliary-Reference-Cited by-同舟云学术

Synthesis of a New (1R)-(−)-Myrtenal-Derived Dioxadithiadodecacycle and Its Use as an Efficient Chiral Auxiliary

Published:2006-12-09 Issue:1 Volume:9 Page:13-16
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Vargas-Díaz M. Elena¹,Joseph-Nathan Pedro¹,Tamariz Joaquín¹,Zepeda L. Gerardo¹

Affiliation:

1. Departamento de Química Orgánica, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prol. de Carpio y Plan de Ayala, México, D.F., 11340 Mexico, and Departamento de Química, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Apartado 14-740, México, D.F., 07000 Mexico

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol062319f

Reference17 articles.

1. A virtually completely asymmetric synthesis

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

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

4. Highly stereoselective asymmetric synthesis of ()-(−)-mevalolactone

5. Asymmetric syntheses based on 1,3-oxathianes. 1. Scope of the reaction

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