EventsThe 18th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 18th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2014
Citation
Francisco Meijide, Juan V. Trillo, Cristina Gancedo, Victor Hugo Soto, Luciano Galantini, Aida Jover, José Vázquez Tato, Santiago de Frutos, Crystal Structure of a Head-to-Head Bis(cholic)-Urea Dimer, in Proceedings of The 18th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2014, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-18-a006
Share
Email
Facebook
Twitter
LinkedIn

Crystal Structure of a Head-to-Head Bis(cholic)-Urea Dimer

Juan V. Trillo 1
Cristina Gancedo 1
Victor Hugo Soto 2
image
1. Universidad de Santiago de Compostela
2. Escuela de Química, Centro de Investigación en Electroquímica y Energía Química (CELEQ), Universidad de Costa Rica, San José, Costa Rica
3. Dipartimento di Chimica, Università di Roma "Sapienza", P. le A. Moro 5, 00185 Roma, Italy
Abstract
A head-to-head dimer of cholic acid linked at C3 carbon atoms by a urea bridge was synthesized and the crystal structure was studied. The crystal belongs to the monoclinic crystal system, space group I2. The packing shows a bilayer structure with alternating hydrophobic and hydrophilic layers. The horizontal and vertical planes of the two cholic residues are almost parallel to each other, the vertical ones being perpendicular to the bilayers. The hydrogen bond network is two-dimensional as it does not propagate in the direction perpendicular to the bilayers. It is noteworthy that the nitrogen atoms of the urea bridge do not participate in that network. The carbonyl urea group and only one of the ester of the two side chains form hydrogen bonds with two other dimers through the steroid hydroxy O7-H and O12-H groups. This means that each dimer forms eight hydrogen bonds but only four are different.
Keywords
Cholic
bile acid
crystal structure
Manuscript
Syntheses and Reactions of 5-Alkyl- and 5-Aryl-11b-Methyl-1,2,3,11b-Tetrahydro-Pyrido[3,2,1-jk]carbazoles Having a Strychnos Alkaloids Partial Structure
Highly Efficient and Chemoselective Synthetic Route to de Thiazolidinones via a Microwave Assisted, Three Component Reaction