Development of a temporary marker for peptides

M. Sameiro; T. Gonçalves; Hernâni L.S. Maia

doi:10.1039/b212470j

Development of a temporary marker for peptides

M. Sameiro, T. Gonçalves, Hernâni L.S. Maia^*

^*Corresponding author for this work

Catalysis Research Center

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

3-[(N,N-Dimethylaminophenyl)-4′-diazenyl]benzoic acid was coupled with several amino acid esters and the product acylated further with Boc. The material thus obtained was then submitted to cleavage by electrolysis and nucleophilic attack in order to evaluate the possibility of using this chromophore as a temporary marker.

Original language	English (US)
Pages (from-to)	1480-1485
Number of pages	6
Journal	Organic and Biomolecular Chemistry
Volume	1
Issue number	9
DOIs	https://doi.org/10.1039/b212470j
State	Published - May 7 2003

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1039/b212470j

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title = "Development of a temporary marker for peptides",

abstract = "3-[(N,N-Dimethylaminophenyl)-4′-diazenyl]benzoic acid was coupled with several amino acid esters and the product acylated further with Boc. The material thus obtained was then submitted to cleavage by electrolysis and nucleophilic attack in order to evaluate the possibility of using this chromophore as a temporary marker.",

author = "M. Sameiro and T. Gon{\c c}alves and Maia, {Hern{\^a}ni L.S.}",

year = "2003",

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language = "English (US)",

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T1 - Development of a temporary marker for peptides

AU - Sameiro, M.

AU - Gonçalves, T.

AU - Maia, Hernâni L.S.

PY - 2003/5/7

Y1 - 2003/5/7

N2 - 3-[(N,N-Dimethylaminophenyl)-4′-diazenyl]benzoic acid was coupled with several amino acid esters and the product acylated further with Boc. The material thus obtained was then submitted to cleavage by electrolysis and nucleophilic attack in order to evaluate the possibility of using this chromophore as a temporary marker.

AB - 3-[(N,N-Dimethylaminophenyl)-4′-diazenyl]benzoic acid was coupled with several amino acid esters and the product acylated further with Boc. The material thus obtained was then submitted to cleavage by electrolysis and nucleophilic attack in order to evaluate the possibility of using this chromophore as a temporary marker.

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U2 - 10.1039/b212470j

DO - 10.1039/b212470j

M3 - Article

AN - SCOPUS:0141905840

SN - 1477-0520

VL - 1

SP - 1480

EP - 1485

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 9

ER -

Development of a temporary marker for peptides

Abstract

ASJC Scopus subject areas

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