Synthesis of N-quinonyltaurines.

Abstract:

:Both 1,4-benzoquinones and 1,4-naphthoquinones were attached to the non-proteinogenic amino acid taurine to form N-quinonyl taurine derivatives. The products were formed via the direct Michael-like addition or by substitution of a good leaving group. An attempt to bridge the two moieties via an ureido spacer resulted in the formation of a bis-quinonylamino isocyanurate derivative. Preliminary MO calculations provided internal ground-state geometries and orbital coefficients of the HOMO levels in two representing taurine conjugates.

journal_name

Amino Acids

journal_title

Amino acids

authors

Gorohovsky S,Temtsin-Krayz G,Bittner S

doi

10.1007/s00726-002-0407-4

subject

Has Abstract

pub_date

2003-04-01 00:00:00

pages

281-7

issue

3

eissn

0939-4451

issn

1438-2199

journal_volume

24

pub_type

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