Enantiomer-Selective Carbamoylation of Racemic α-Hydroxy γ-Lactones with Chiral CuIICatalysts: An Example of a Highly Active Lewis Acid Catalyzed Reaction-Reference-Cited by-同舟云学术

Enantiomer-Selective Carbamoylation of Racemic α-Hydroxy γ-Lactones with Chiral CuIICatalysts: An Example of a Highly Active Lewis Acid Catalyzed Reaction

Published:2008-09-01 Issue:8-9 Volume:3 Page:1289-1297
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Kurono Nobuhito,Kondo Tadahiro,Wakabayashi Masanori,Ooka Hirohito,Inoue Tsutomu,Tachikawa Hiroto,Ohkuma Takeshi

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Reference61 articles.

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2. For pioneering works on asymmetric reactions with box-metal catalysts, see:

3. Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins

4. Designed catalyst for enantioselective Diels-Alder addition from a C2-symmetric chiral bis(oxazoline)-iron(III) complex

5. For recent reviews, see:

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