Diastereoselective Michael reaction of chiral nickel(II) glycinate with nitroalkenes for asymmetric synthesis of β-substituted α,γ-diaminobutyric acid derivatives in water.

Abstract:

:We have developed the first operationally simple and environmentally benign protocol for the aqueous asymmetric Michael addition reaction of chiral nickel(II) glycinate with nitroalkenes. The reactions proceeded smoothly in the presence of TBAB (tetrabutyl ammonium bromide) in neat water at room temperature and provided good yields of β-substituted α,γ-diaminobutyric acid derivatives with excellent diastereoselectivities.

journal_name

Amino Acids

journal_title

Amino acids

authors

Wang J,Ji X,Shi J,Sun H,Jiang H,Liu H

doi

10.1007/s00726-011-0870-x

subject

Has Abstract

pub_date

2012-05-01 00:00:00

pages

1685-94

issue

5

eissn

0939-4451

issn

1438-2199

journal_volume

42

pub_type

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