The readily available tert-pentyl group as a most effective simple directing group for asymmetric synthesis: a case study on Salen–Mn(III)-catalyzed epoxidation-Reference-Cited by-同舟云学术

The readily available tert-pentyl group as a most effective simple directing group for asymmetric synthesis: a case study on Salen–Mn(III)-catalyzed epoxidation

Published:2002-10 Issue:19 Volume:13 Page:2089-2093
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Gaquere Anne,Liang Sidney,Hsu Fu-Lian,Bu Xiu R

Publisher

Elsevier BV

Subject

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

Reference16 articles.

1. Catalytic Asymmetric Oxidation of tert-Butyl Disulfide. Synthesis of tert-Butanesulfinamides, tert-Butyl Sulfoxides, and tert-Butanesulfinimines

2. Asymmetric Sulfide Oxidation with Vanadium Catalysts and H2O2

3. Catalytic, Enantioselective Aldol Additions with Methyl and Ethyl Acetate O-Silyl Enolates: A Chiral Tridentate Chelate as a Ligand for Titanium(IV)

4. Chiral Lewis Acid Catalysis in Radical Reactions: Enantioselective Conjugate Radical Additions

5. Chiral Bis(oxazoline) Copper(II) Complexes: Versatile Catalysts for Enantioselective Cycloaddition, Aldol, Michael, and Carbonyl Ene Reactions

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