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Volumn 8, Issue 13, 2007, Pages 1504-1508

Metal-free triazole formation as a tool for bioconjugation

Author keywords

Click reaction; Conjugation; Cycloadditions; Retro Diels Alder; Triazoles

Indexed keywords

1,2,3 TRIAZOLE DERIVATIVE; 1,4,5 TRIAZOLE DERIVATIVE; ALKADIENE; METAL; OXANORBORNADIENE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34548715186     PISSN: 14394227     EISSN: 14397633     Source Type: Journal    
DOI: 10.1002/cbic.200700278     Document Type: Article
Times cited : (188)

References (51)
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    • N. J. Agard, J. A. Prescher, C. R. Bertozzi, J. Am. Chem. Soc. 2004, 126, 15046-15047; erratum:
    • a) N. J. Agard, J. A. Prescher, C. R. Bertozzi, J. Am. Chem. Soc. 2004, 126, 15046-15047; erratum:
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    • For a detailed experimental procedure see the Supporting Information
    • For a detailed experimental procedure see the Supporting Information.
  • 51
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    • Initial experiments have shown that Michael addition processes can, to a minor extent, interfere with the reported ligation method. In short, 2 b was incubated with a pool of all 20 naturally occurring amino acids (in excess) in phosphate buffer at room temperature for 72 h. For the basic amino-acid residues (i.e., Lys, Arg, His) traces of addition products with 2 b could be detected. Adducts of Cys could not be detected, but are likely to be formed.
    • Initial experiments have shown that Michael addition processes can, to a minor extent, interfere with the reported ligation method. In short, 2 b was incubated with a pool of all 20 naturally occurring amino acids (in excess) in phosphate buffer at room temperature for 72 h. For the basic amino-acid residues (i.e., Lys, Arg, His) traces of addition products with 2 b could be detected. Adducts of Cys could not be detected, but are likely to be formed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.