Literature DB >> 20461274

Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt.

Masanori Yoshida1, Atsushi Sato, Shoji Hara.   

Abstract

Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by asymmetric catalysis with L-phenylalanine lithium salt, giving gamma-nitroaldehydes in good yields with high enantioselectivity.

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Year:  2010        PMID: 20461274     DOI: 10.1039/c003940c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Asymmetric Michael Addition Organocatalyzed by α,β-Dipeptides under Solvent-Free Reaction Conditions.

Authors:  C Gabriela Avila-Ortiz; Lenin Díaz-Corona; Erika Jiménez-González; Eusebio Juaristi
Journal:  Molecules       Date:  2017-08-10       Impact factor: 4.411

  1 in total

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