Literature DB >> 20882598

Structural influence of chiral tertiary aminonaphthol ligands on the asymmetric phenyl transfer to aromatic aldehydes.

Hui Wei1, Lu Yin, Haibin Luo, Xingshu Li, Albert S C Chan.   

Abstract

A series of chiral tertiary aminonaphthol ligands were prepared from 2-naphthol, (S)-1-phenylethylamine, and aldehydes with diverse substituted groups. The results of asymmetric phenyl transfer to aromatic aldehydes catalyzed by these chiral ligands indicated that enantioselectivities were greatly influenced by the electronic and steric effects of the ligands.
Copyright © 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20882598     DOI: 10.1002/chir.20903

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  2 in total

Review 1.  Recent advances in the synthesis and synthetic applications of Betti base (aminoalkylnaphthol) and bis-Betti base derivatives.

Authors:  Abolfazl Olyaei; Mahdieh Sadeghpour
Journal:  RSC Adv       Date:  2019-06-11       Impact factor: 4.036

Review 2.  New Advances in the Synthetic Application of Enantiomeric 1-Phenylethylamine (α-PEA): Privileged Chiral Inducer and Auxiliary.

Authors:  Marzena Wosińska-Hrydczuk; Jacek Skarżewski
Journal:  Molecules       Date:  2020-10-23       Impact factor: 4.411

  2 in total

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