Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Paula K. Kuroishi"'
Autor:
Haritz Sardon, Paula K. Kuroishi, Didier Gigmes, Andrew P. Dove, Frédéric Dumur, Nicolas Zivic
Publikováno v:
Angewandte Chemie. 131:10518-10531
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b006555571edf1329d2d4185db84eb62
https://doi.org/10.1002/ange.201810118
https://doi.org/10.1002/ange.201810118
Autor:
Andrew P. Dove, Paula K. Kuroishi
Publikováno v:
Chemical Communications. 54:6264-6267
The phototriggered ring-opening polymerisation of l-lactide is demonstrated for the first time using a photocaged tetramethylguanidine. The catalytic activity of the free guanidine was also investigated, showing it to be active for the polymerisation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24390c5be3f1444d17dda666807571ca
https://doi.org/10.1039/c8cc01913d
https://doi.org/10.1039/c8cc01913d
Publikováno v:
Polymer Chemistry. 7:7108-7115
The synthesis of an epoxide-functional polycarbonate via the selective carbonate ring-opening polymerisation (ROP) of trimethylenepropane oxirane ether carbonate (TMOC) monomer was investigated using a range of organocatalysts. The catalyst 1,5,7-tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b9e72cde13c467bd6aa1752811bce0
https://doi.org/10.1039/c6py01636g
https://doi.org/10.1039/c6py01636g
Autor:
Paula K. Kuroishi, Andrew P. Dove
Publikováno v:
Nature Catalysis. 1:486-487
Control over the length and composition of polymers is key to controlling their properties. Now, a photoswitchable catalyst is shown to allow external control over reaction rates, chain lengths and even polymer composition in ring-opening polymerizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bec3c7ddedfc761aeda8c05762114579
https://doi.org/10.1038/s41929-018-0112-7
https://doi.org/10.1038/s41929-018-0112-7
Publikováno v:
European Polymer Journal. 120:109192
Features such as the renewability and biodegradability of polylactide (PLA) have resulted in numerous applications in biomedical and commodity polymers. However, the brittle nature of PLA hinders its wider implementation; consequently, investigations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31565269b49eb820762e4497912565b2
https://doi.org/10.1016/j.eurpolymj.2019.08.019
https://doi.org/10.1016/j.eurpolymj.2019.08.019
Autor:
Andrew K. Whittaker, Maria M. Pérez-Madrigal, Andrew P. Dove, Paula K. Kuroishi, Anthony W. Thomas
Publikováno v:
Polymer Chemistry
Thermally-responsive polymers have been widely studied, however access to materials in which both the thermal response can be tuned and in which the backbone is ultimately biodegradable is limited. To this end, a range of well-defined homopolymers of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc471b210782903d7c8f509388eb128
https://hdl.handle.net/2117/380178
https://hdl.handle.net/2117/380178
Publikováno v:
ChemInform. 46
A stereoselective total synthesis of (−)-cryptocaryol A (1) is described. Key features of the 17-step route include the use of three boron-mediated aldol reaction–reduction sequences to control all stereocenters and an Ando modification of the Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1daac0fd00e18ced4d5a4e90743ffaeb
https://doi.org/10.1002/chin.201529253
https://doi.org/10.1002/chin.201529253
Publikováno v:
Organicbiomolecular chemistry. 13(12)
A stereoselective total synthesis of (−)-cryptocaryol A (1) is described. Key features of the 17-step route include the use of three boron-mediated aldol reaction–reduction sequences to control all stereocenters and an Ando modification of the Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d78bc25a18f116de149c2ebfccb12e61
https://pubmed.ncbi.nlm.nih.gov/25695350
https://pubmed.ncbi.nlm.nih.gov/25695350
Publikováno v:
Tetrahedron Letters. (8):980-982
The first total synthesis of (−)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3690bd22792d38d89a91153d56cd4153