期刊
POLYHEDRON
卷 39, 期 1, 页码 9-13出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.poly.2012.03.003
关键词
Antitumor agents; Boron neutron capture therapy; Carboranes; Carbaboranes; Glycosides; Thiols
资金
- Fonds der Chemischen Industrie (FCI)
- European Union
- Free State of Saxony (EFRE)
- Graduate School of Excellence Leipzig School of Natural Sciences - Building with Molecules and Nano-objects (BuildMoNa)
- Erasmus Mundus ASC
The potential of 1,2-dicarba-closo-dodecaborane(12)-9-thiol, 9-HS-1,2-closo-C2B10H11, for the design of novel building blocks is highlighted by two examples envisioned for incorporation into tumor-selective peptides for boron neutron capture therapy (BNCT). By employing a t-Bu protection strategy the synthesis of a bis-galactosyl-substituted ortho-carbaborane carboxylic acid was elaborated, and the procedure is suggested as a general approach towards carbaboranes with three substituents. Furthermore, a simple route to a tris(ortho-carbaborane) building block starting from pentaerythritol is illustrated. All compounds were synthesized in moderate to high yields and identified by H-1, B-11, and C-13 NMR spectroscopy, IR spectroscopy, mass spectrometry, and in one case by X-ray crystallography. (C) 2012 Elsevier Ltd. All rights reserved.
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