RT Book,_Section
T1 Synthesis and characterization of new tail-to-tail dimers of bile acids with different spacers
A1 Antelo Queijo, Álvaro
A1 Álvarez Alcalde, María de las Mercedes
A1 Jover Ramos, Aida
A1 Meijide del Río, Francisco Ángel
A1 Vázquez Tato, José
AB New dimeric steroid-based surfactants derived from 3α,7α,12α-trihydroxy-5β- cholan-24-amine (steroid residue) and isophthalic acid, 5,5'-biisobenzofuran-1,1',3,3'- carboxylic acid and succinic acid (spacers) were synthesized and structurally characterized by NMR techniques. The first spacer was also employed to synthesize the dimer corresponding to the 3α,12α-dihydroxy-5β-cholan-24-amine residue. In all cases the steroid residues are tail-to-tail linked through amide bonds with the spacers
PB MDPI
SN 3-906980-23-5
YR 2009
FD 2009
LK http://hdl.handle.net/10347/26860
UL http://hdl.handle.net/10347/26860
LA eng
NO Vázquez Tato, J.; Meijide, F.; Jover, A.; Álvarez Alcalde, M.; Antelo, Á. Synthesis and characterization of new tail-to-tail dimers of bile acids with different spacers, in Proceedings of the 13th International Electronic Conference on Synthetic Organic Chemistry, 1–30 November 2009, MDPI: Basel, Switzerland, doi:10.3390/ecsoc-13-00256
NO The 13th International Electronic Conference on Synthetic Organic Chemistry session Polymer and Supramolecular Chemistry
NO Authors thank the Ministerio de Ciencia y Tecnología (Project MAT2004-04606) and the Xunta de Galicia (PGIDIT05PXIC26201PN) for financial support
DS Minerva
RD 24 abr 2026