Peptide analogues of DNA consisting of L-α-amino-γ-thymine butyric acid and L-valine subunits

Article abstract of DOI:10.1080/15257779508012478

Reaction of N-Boc-L-homoserine benzylester with N³-benzoylthymine under Mitsunobu conditions afforded N-Boc-L-α-amino-γ-N³-benzoylthymine butyric acid benzylester. After removal of the N-benzoyl and O-benzyl protecting group, this compound was used in solution phase peptide synthesis.

Full text of DOI:10.1080/15257779508012478

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Peptide Analogues of DNA Consisting of
l-α-Amino-γ-thymine Butyric Acid and l-
Valine Subunits
G. Ceulemans a , K. Khan a , A. Van Schepdael a & P. Herdewijn a
a Rega Institute for Medical Research, Laboratory of Medicinal
Chemistry , Faculty of Pharmacy Katholieke Universiteit Leuven ,
B-3000, Leuven, Belgium
Published online: 16 Feb 2007.
To cite this article: G. Ceulemans , K. Khan , A. Van Schepdael & P. Herdewijn (1995) Peptide
Analogues of DNA Consisting of l-α-Amino-γ-thymine Butyric Acid and l-Valine Subunits, Nucleosides
and Nucleotides, 14:3-5, 813-816
To link to this article: http://dx.doi.org/10.1080/15257779508012478
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