Amino Acids, Peptides and Proteins in Organic Chemistry 2011
DOI: 10.1002/9783527631827.ch15
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Amino Acid‐Based Dendrimers

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Cited by 2 publications
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“…The presence of bifunctional N α -and N ε -amino groups in each lysine served as reactive ends for the conjugation. 49 In amino groups of N ε -terminal of lysine residues, 4-pentynoic acids were coupled to introduce the alkyne functionalities whereas, amino acids of PADRE sequence and acyl group were sequentially coupled to N α -terminal sites of lysine residues. Azido-functionalized J8 peptide (QAEDKVKQSREAKKQ-VEKALKQLEDKVQ) was also synthesized using the same technique.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…The presence of bifunctional N α -and N ε -amino groups in each lysine served as reactive ends for the conjugation. 49 In amino groups of N ε -terminal of lysine residues, 4-pentynoic acids were coupled to introduce the alkyne functionalities whereas, amino acids of PADRE sequence and acyl group were sequentially coupled to N α -terminal sites of lysine residues. Azido-functionalized J8 peptide (QAEDKVKQSREAKKQ-VEKALKQLEDKVQ) was also synthesized using the same technique.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…This process was continued to conjugate immunosilent two-branched lysine dendrimer. The presence of bifunctional N α - and N ε -amino groups in each lysine served as reactive ends for the conjugation . In amino groups of N ε -terminal of lysine residues, 4-pentynoic acids were coupled to introduce the alkyne functionalities whereas, amino acids of PADRE sequence and acyl group were sequentially coupled to N α -terminal sites of lysine residues.…”
Section: Results and Discussionmentioning
confidence: 99%