Solvent-induced chirality switching in the enantioseparation of regioisomeric hydroxyphenylpropionic acids via diastereomeric salt formation with (1 R ,2 S )-2-amino-1,2-diphenylethanol-Reference-Cited by-同舟云学术

Solvent-induced chirality switching in the enantioseparation of regioisomeric hydroxyphenylpropionic acids via diastereomeric salt formation with (1 R ,2 S )-2-amino-1,2-diphenylethanol

Published:2017-03 Issue:3 Volume:28 Page:460-466
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Kodama Koichi,Nagata Jun,Kurozumi Nobuhiro,Shitara Hiroaki,Hirose Takuji

Funder

JSPS

Publisher

Elsevier BV

Subject

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

Reference32 articles.

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5. Direct enantioseparation of diarylmethylamines with an ortho-hydroxy group via diastereomeric salt formation and their application to the enantioselective addition reaction of diethylzinc

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