Regioselective Synthesis of V‑Shaped Bistriazinyl-phenanthrolines

Dataset UNKNOWN
Coogan, Niall T.; Chimes, Michael A.; Raftery, James; Mocilac, Pavle; Denecke, Melissa A.;
(2015)
  • Publisher: Figshare
  • Related identifiers: doi: 10.1021/acs.joc.5b01380.s001, doi: 10.1021/acs.joc.5b01380.s002, doi: 10.1021/acs.joc.5b01380.s003, doi: 10.1021/acs.joc.5b01380.s004
  • Subject: isomer | Biotechnology | access | bi | intramolecular | derivative | crystal structures | ligand | Ecology | XPhBTPhen | reagent | Pharmacology | yield | precursor | hydrazono | Molecular | bromo | Described | synthesis | BTPhen | isomers | method | Developmental Biology | oxime | regioselective | Computational Biology | Cell Biology | phenyl | future supramolecular actinide complexing systems | PhBTPhen | Biochemistry | solubility | chloro | PhBTP | Synthesi
    • FOR: 39999 Chemical Sciences not elsewhere classified

A new, regioselective synthesis of V-shaped 2,9-bis­(6-(4-halophenyl)-1,2,4-triazin-3-yl)-1,10-phenanthrolines (4XPhBTPhen) ligands was developed, creating access to a simple and reliable synthesis of precursors for future supramolecular actinide complexing ... View more
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