Issue 18, 1998
From the journal:

Chemical Communications

Stereoselective and N-terminal selective α-alkylation of peptides using a pyridoxal model compound as a chiral N-terminal activator

Kazuyuki Miyashita,   Hiroshi Iwaki,   Kuninori Tai,   Hidenobu Murafuji  and  Takeshi Imanishi  

Abstract

Stereoselective and N-terminal selective α-alkylation of peptides is achieved using a pyridoxal model compound as an N-terminal activator which also functions as a chiral auxiliary.

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Article information

DOI
https://doi.org/10.1039/A805596C
Article type
Paper

Chem. Commun., 1998, 1987-1988

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Stereoselective and N-terminal selective α-alkylation of peptides using a pyridoxal model compound as a chiral N-terminal activator

K. Miyashita, H. Iwaki, K. Tai, H. Murafuji and T. Imanishi, Chem. Commun., 1998, 1987 DOI: 10.1039/A805596C

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