Synthesis and Investigation of Linker-Free BODIPY–Gly Conjugates Substituted at the Boron Atom

An efficient synthesis of boron-functionalized cyclic BODIPY–Gly conjugates, using commercially available N-protected glycine amino acids and a BF2–BODIPY moiety as starting materials, is reported. The existence of two conformers (up and down) is revealed through comprehensive DFT calculations and 1...

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Veröffentlicht in:Inorganic chemistry 2019-09, Vol.58 (17), p.11614-11621
Hauptverfasser: Wang, Maodie, Zhang, Guanyu, Bobadova-Parvanova, Petia, Merriweather, Ashley N, Odom, Lilian, Barbosa, David, Fronczek, Frank R, Smith, Kevin M, Vicente, M. Graça H
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Sprache:eng
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