Journal
POLYHEDRON
Volume 30, Issue 9, Pages 1494-1501Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.poly.2011.02.055
Keywords
closo-Decaborate; Oxonium derivatives; Carboxylic acids; Protonation
Categories
Funding
- Russian Foundation for Basic Research [08-03-00463]
- Russian Academy of Sciences
Ask authors/readers for more resources
A series of new boron-containing carboxylic acids was prepared by the ring-opening reaction of cyclic oxonium derivatives of the c/oso-decaborate anion [B10H10](2-) with methyl esters of hydroxybenzoic acids or the cyanide anion followed by hydrolysis of the obtained nitrile and esters. Acid hydrolysis of the esters results in protonation of the oxygen atom connected to the boron cage, with the formation of the corresponding P-protonated acids, isolated in the solid state. The compounds synthesized can be used in radionuclide diagnostics and boron neutron capture therapy of cancer. (C) 2011 Elsevier Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available