4.4 Article

Recent Developments in the Synthesis of Bioactive 2,4,6-Trisubstituted 1,3,5-Triazines

期刊

SYNLETT
卷 24, 期 13, 页码 1599-1605

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0033-1339284

关键词

cyanuric chloride; nucleophilic substitution; solid-phase; solution-phase; library synthesis

资金

  1. Damon Runyon Cancer Research Foundation [DRR-18-12]
  2. Smith Family Foundation
  3. Boston College

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1,3,5-Triazine derivatives have widespread applications in the pharmaceutical, material, and agrochemical industries. In the biological arena, small-molecule libraries of 2,4,6-trisubstituted 1,3,5-triazines have yielded selective and potent chemical probes for diverse protein families. The structural symmetry and ease of functionalization of the 1,3,5-triazine core renders it a powerful scaffold for the rapid generation of diverse molecular libraries. Numerous synthetic routes, both solid-phase and solution-phase, have been developed to arrive at alkyl/aryl amino-and oxy-substituted triazine libraries. Here, we feature a subset of the recent synthetic advances towards generating 2,4,6-trisubstituted 1,3,5-triazines and highlight biologically active compounds that have resulted from these endeavors.

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