Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ellen M. G. Jamieson"'
Autor:
Noel Pairault, Federica Rizzi, David Lozano, Ellen M. G. Jamieson, Graham J. Tizzard, Stephen M. Goldup
Catenanes—molecules comprising two interlocking rings held together like links in a chain—are topologically non-trivial: a catenane is a topological isomer of its separated rings, but the rings cannot be disconnected without bond scission. Catena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206549d788d483ce4ba493c474965266
https://eprints.soton.ac.uk/477475/
https://eprints.soton.ac.uk/477475/
Autor:
David B. Cordes, Ellen M. G. Jamieson, Alexandra M. Z. Slawin, Douglas Philp, Leonardo Maugeri
Publikováno v:
Chemical Science. 8:938-945
We thank the Marie Curie Initial Training Network on Replication and Adaption in Networks (ReAd) for financial support (early stage researcher funding to L. M.). Phenols and their corresponding phenoxide anions can form halogen bonds with neutral iod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6479e83a25b5842dab25943ad831e24c
https://doi.org/10.1039/c6sc03696a
https://doi.org/10.1039/c6sc03696a
Publikováno v:
Nature Chemistry
Interlocked molecules can exhibit chiral stereogenic elements that are not found in covalently bound systems. Now, the shuttling of the ring in a [2]rotaxane has been shown to result in enantiomeric co-conformations that selectively bind chiral guest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2543100395a7fe1af4d5cb27c73ecac
https://pubmed.ncbi.nlm.nih.gov/31444487
https://pubmed.ncbi.nlm.nih.gov/31444487
Autor:
Florian Modicom, Catherine J. Fletcher, Mathieu Denis, Stephen M. Goldup, Ellen M. G. Jamieson, Marzia Galli, Michael A. Jinks, Zhihui Zhang, Alberto de Juan
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
Chiral interlocked molecules in which the mechanical bond provides the sole stereogenic unit are typically produced with no control over the mechanical stereochemistry. Here we report a stereoselective approach to mechanically planar chiral rotaxanes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02032080eb9b793cae5ad9b49f7530a2
https://eprints.soton.ac.uk/423566/
https://eprints.soton.ac.uk/423566/
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
We report the unexpected discovery of a tandem active template CuAAC‐rearrangement process, in which N2 is extruded on the way to the 1,2,3‐triazole product to give instead acrylamide rotaxanes. Mechanistic investigations suggest this process is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5507cb319b6a084c2284bfd811574d0