New 1,3-Oxathianes Derived from Myrtenal: Synthesis and Reactivity-Reference-Cited by-同舟云学术

New 1,3-Oxathianes Derived from Myrtenal: Synthesis and Reactivity

Published:2003-07-19 Issue:17 Volume:68 Page:6619-6626
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Solladié-Cavallo Arlette¹,Balaz Milan¹,Salisova Marta¹,Welter Richard¹

Affiliation:

1. Département de Chimie Organique Fine, ECPM/Université Louis Pasteur, 67087-Strasbourg, France, Department of Organic Chemistry, Comenius University, 842 15-Bratislava, Slovakia, and Laboratoire DECMET, UMR 7513, Université Louis Pasteur, 67000 Strasbourg

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034404w

Reference23 articles.

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

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

3. 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.

4. Martinez-Ramos, F.; Vargas-Diaz, M. E.; Chacon-Garcia, L.; Tamariz, J.; Joseph-Nathan, P.; Zepeda, L. G.Tetrahedron: Asymmetry2001,12, 3095.

5. (a) Solladié-Cavallo, A.; Balaz, M.; Salisova, M.; Suteu, C.; Nafie, L. A.; Cao, X.; Freedman T. B.Tetrahedron: Asymmetry2001,12,2605.

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