Affiliations 

  • 1 Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung, Taiwan
  • 2 Department of Pharmacy, National Yang Ming Chiao Tung University, Taipei, Taiwan
  • 3 Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan
  • 4 Department of Chemistry, University of Malaya, Kuala Lumpur, Malaysia
  • 5 Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung, Taiwan. clkao@kmu.edu.tw
Methods Mol Biol, 2025;2931:177-186.
PMID: 40531457 DOI: 10.1007/978-1-0716-4562-8_14

Abstract

In conventional dendrimer synthesis, producing defective dendrimers is unavoidable. However, no synthetic method exists to prepare these defect dendrimers with a well-defined structure. A novel and efficient solid-phase method has been developed to synthesize well-defined lysine defect dendrimers using orthogonally protected lysine residues. This chapter details the synthesis of two defect lysine dendrimers. Additionally, the synthesis of a boronic acid-decorated defect lysine dendrimer is presented to demonstrate the feasibility of this method for preparing functional defect dendrimers.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.