The use of co-crystals for the determination of absolute stereochemistry: an alternative to salt formation
dc.contributor.author | Eccles, Kevin S. | |
dc.contributor.author | Deasy, Rebecca E. | |
dc.contributor.author | Fábián, László | |
dc.contributor.author | Maguire, Anita R. | |
dc.contributor.author | Lawrence, Simon E. | |
dc.contributor.funder | Science Foundation Ireland | en |
dc.contributor.funder | Irish Research Council for Science Engineering and Technology | en |
dc.contributor.funder | Eli Lilly and Company, United States | en |
dc.date.accessioned | 2013-01-30T11:12:12Z | |
dc.date.available | 2013-01-30T11:12:12Z | |
dc.date.copyright | 2011-01 | |
dc.date.issued | 2011-01 | |
dc.date.updated | 2012-12-21T09:27:35Z | |
dc.description.abstract | Absolute stereochemistry of oils and viscous liquids can be difficult to determine. Co-crystallization involves generating a crystalline material consisting of more than one neutral compound. The combination of cocrystallization with both X-ray diffraction and chiral HPLC was particularly powerful in overcoming these difficulties for a series of chiral 3-arylbutanoic acids. Cocrystallization offers advantages over salt formation because co-crystals dissociate in solution, meaning identical HPLC conditions can be used for both the materials of interest and their co-crystals. | en |
dc.description.sponsorship | Science Foundation Ireland (08/RFP/MTR1664); Science Foundation Ireland (07/SRC/B1158); Science Foundation Ireland (05/PICA/B802); Science Foundation Ireland (TIDA 09); Science Foundation Ireland (05/PICA/B802/EC07) | en |
dc.description.status | Peer reviewed | en |
dc.description.version | Accepted Version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | Eccles, Kevin S., Deasy,Rebecca E., Fabian, Laszlo, Maguire, Anita R., Lawrence, Simon E. (2011) 'The Use of Co-crystals for the Determination of Absolute Stereochemistry: An Alternative to Salt Formation'. Journal of Organic Chemistry, 76 (4):1159-1162. http://pubs.acs.org/doi/abs/10.1021/jo102148p | en |
dc.identifier.doi | 10.1021/jo102148p | |
dc.identifier.endpage | 1162 | en |
dc.identifier.issn | 0022-3263 | |
dc.identifier.issued | 4 | en |
dc.identifier.journaltitle | Journal of Organic Chemistry | en |
dc.identifier.startpage | 1159 | en |
dc.identifier.uri | https://hdl.handle.net/10468/944 | |
dc.identifier.volume | 76 | en |
dc.language.iso | en | en |
dc.publisher | American Chemical Society | en |
dc.relation.uri | http://pubs.acs.org/doi/abs/10.1021/jo102148p | |
dc.rights | © 2011, American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Crystal Growth & Design, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/jo102148p | en |
dc.subject | Stereochemistry | en |
dc.subject | Co-crystallization | en |
dc.subject | X-ray diffraction | en |
dc.subject | Chiral HPLC | en |
dc.subject.lcsh | Crystallization | en |
dc.title | The use of co-crystals for the determination of absolute stereochemistry: an alternative to salt formation | en |
dc.type | Article (peer-reviewed) | en |