(R)- and (S)-3-hydroxy-4,4-dimethyl-1-phenyl-2-pyrrolidinone by lipase-catalyzed resolution of the racemic mixture: New chiral auxiliaries related to pantolactone-Reference-Cited by-同舟云学术

(R)- and (S)-3-hydroxy-4,4-dimethyl-1-phenyl-2-pyrrolidinone by lipase-catalyzed resolution of the racemic mixture: New chiral auxiliaries related to pantolactone

Published:1995-04 Issue:4 Volume:6 Page:985-990
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Camps Pelayo,Giménez Sílvia,Font-Bardia Mercè,Solans Xavier

Publisher

Elsevier BV

Subject

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

Reference20 articles.

1. .alpha.-Hydroxy esters as chiral reagents: asymmetric synthesis of 2-arylpropionic acids

2. Asymmetric synthesis of ketoprofen : A surprising base catalyst effect during asymmetric addition of pantolactone to methyl (3-benzoylphenyl) ketene

3. Enantioselective Synthesis of 1,3-Dioxygen-substituted Chiral Building Blocks

4. Reaction of (R)-pantolactone esters of alpha-bromoacids with amines a remarkable synthesis of optically active alpha-amino esters

5. Stereoselective SN2 Reactions of the (R)-Pantolactone Ester of Racemic .alpha.-Halo Carboxylic Acids with Aryl Oxides. A Synthesis of (S)-2-Aryloxy and (S)-2-Hydroxy Acids

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