Regio- and diastereoselectivity in TiCl4-promoted reduction of 2-aryl-substituted cis-4-methyl-5-trifluoromethyl-1,3-dioxolanes-Reference-Cited by-同舟云学术

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Regio- and diastereoselectivity in TiCl4-promoted reduction of 2-aryl-substituted cis-4-methyl-5-trifluoromethyl-1,3-dioxolanes

Published:2002-11 Issue:23 Volume:13 Page:2609-2618
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Morelli Carlo F.,Fornili Arianna,Sironi Maurizio,Durı̀ Lavinia,Speranza Giovanna,Manitto Paolo

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference24 articles.

1. (a) Seebach, D.; Imwinkeheid, R.; Weber, T. In Modern Synthetic Methods; Scheffold, R., Ed.; Springer-Verlag: Berlin, 1986; Vol. 4, pp. 125–259;

2. (b) Alexakis, A.; Mangeney, P. Tetrahedron: Asymmetry 1990, 1, 477–511;

3. (c) Ishihara, K.; Mori, A.; Yamamoto, H. Tetrahedron 1990, 46, 4595–4612.

4. Studies on the mechanism and origin of stereoselective opening of chiral dioxane acetals

5. Mechanism of Chiral Lewis Acid Mediated Enantiotopic Group-Selective Ring Cleavage of Cyclic Acetals Derived from meso-1,2-Diols

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3. Enantioselective Synthesis of Dideoxy-tetrafluorinated Hexoses;The Journal of Organic Chemistry;2016-04-06

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