| dc.contributor.author | Chronakis, Nikos | en |
| dc.creator | Chronakis, Nikos | en |
| dc.date.accessioned | 2019-11-21T06:17:45Z | |
| dc.date.available | 2019-11-21T06:17:45Z | |
| dc.date.issued | 2014 | |
| dc.identifier.issn | 1477-0520 | |
| dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/55344 | |
| dc.description.abstract | Inherently chiral multi-adducts of [60]fullerene represent unique chiral molecular tectons featuring fascinating optoelectronic properties. Herein we discuss the most recent progress in the synthesis of enantiomerically pure bis- and trisadducts of C60with the inherently chiral trans-3 and all-trans-3 addition patterns utilizing cyclo-[n]-malonate tethers derived from (-)-dimethyl-2,3-O-isopropylidene-L-tartrate. Some future perspectives regarding the investigation of these chiral building blocks in modern areas of research are discussed. © The Royal Society of Chemistry 2014. | en |
| dc.source | Organic and Biomolecular Chemistry | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84908043085&doi=10.1039%2fc4ob01666a&partnerID=40&md5=66db0d04b6ab9390826990565fe7fc5c | |
| dc.subject | L-tartaric acids | en |
| dc.subject | Tris-adducts | en |
| dc.title | The journey of L-tartaric acid in the world of enantiomerically pure bis- and trisadducts of C60with the inherently chiral trans-3 and all-trans-3 addition patterns | en |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.doi | 10.1039/c4ob01666a | |
| dc.description.volume | 12 | |
| dc.description.issue | 43 | |
| dc.description.startingpage | 8574 | |
| dc.description.endingpage | 8579 | |
| dc.author.faculty | 002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
| dc.author.department | Τμήμα Χημείας / Department of Chemistry | |
| dc.type.uhtype | Article | en |
| dc.source.abbreviation | Org.Biomol.Chem. | en |
| dc.contributor.orcid | Chronakis, Nikos [0000-0002-2726-5290] | |
| dc.gnosis.orcid | 0000-0002-2726-5290 | |
