Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Liam J. Bromhead"'
Autor:
Maria Chatzopoulou, Katrina S. Madden, Liam J. Bromhead, Christopher Greaves, Thomas J. Cogswell, Solange Da Silva Pinto, Sébastien R. G. Galan, Irene Georgiou, Matthew S. Kennedy, Alice Kennett, Geraint Apps, Angela J. Russell, Graham M. Wynne
Publikováno v:
ACS Medicinal Chemistry Letters. 13:262-270
Palladium-catalyzed reactions are among the most commonly used procedures in organic synthesis. The products have a range of uses, including as intermediates in total synthesis and as screening compounds for drug discovery or agrochemical projects. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0314b69ec7fbe32e5300d6f3aae3078
https://doi.org/10.1021/acsmedchemlett.1c00638
https://doi.org/10.1021/acsmedchemlett.1c00638
Publikováno v:
European Journal of Organic Chemistry. 2017:5712-5723
The generation of molecules that promote plant growth provides opportunities for synthetic chemists to make lasting contributions to the agricultural sector. This Microreview highlights the approaches that have been used to access single enantiomers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bf7cc68756f846339f481fdeae5d6cd
https://doi.org/10.1002/ejoc.201700865
https://doi.org/10.1002/ejoc.201700865
Publikováno v:
Organicbiomolecular chemistry. 16(30)
An enantioselective synthesis of the phenyl ring-containing strioglactone, (-)-solanocol, is described. Application of a Dynamic Kinetic Resolution (DKR) in the stereo-defining step enabled a step-economical synthesis to be achieved, and allowed acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3d95cbc3a81cc06c15a9e1beb9557e0
https://pubmed.ncbi.nlm.nih.gov/30027185
https://pubmed.ncbi.nlm.nih.gov/30027185
Autor:
Einav Mayzlish-Gati, Eduard Belausov, Christopher S. P. McErlean, Liam J. Bromhead, Hinanit Koltai, Yoram Kapulnik, Cristina Prandi, Mohamad Abu-Abied, Hila Haor, Smadar Wininger, Nirali Pandya-Kumar, Anandamoy Dam, Manoj Kumar
Publikováno v:
Journal of Experimental Botany
Highlight This study provides an insight into the cellular events of cytoskeleton rearrangement, vesicle trafficking, and PIN protein localization that are associated with low-Pi response and are dependent on strigolactone-auxin cross-talk.
Stri
Stri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2926d1b251c7284947b2b3d5537ba5bf
https://doi.org/10.1093/jxb/eru513
https://doi.org/10.1093/jxb/eru513
Autor:
Moran Mazuz, Aurel Ion, Puja Kumari, Mohamad Abu-Abied, Smadar Wininger, Cristina Prandi, Christopher S. P. McErlean, Hinanit Koltai, Liam J. Bromhead, Yoram Kapulnik, Einav Mayzlish-Gati, Eduard Belausov, Rafael Perl-Treves, Anandamoy Dam, Ortal Madmon
MAX2/strigolactone signaling in the endodermis and/or quiescent center of the root is partially sufficient to exert changes in F-actin density and cellular trafficking in the root epidermis, and alter gene expression during plant response to low Pi c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cb3dbc502993076048dea051a7305f5
http://hdl.handle.net/2318/1589880
http://hdl.handle.net/2318/1589880
Publikováno v:
ChemInform. 45
A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A–C ring system.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8db6b7b7266b4b38c1e3893951e1315d
https://doi.org/10.1002/chin.201430212
https://doi.org/10.1002/chin.201430212
Publikováno v:
The Journal of organic chemistry. 79(3)
A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A–C ring system.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c80d8a103d8adcd62b27d0798576f765
https://pubmed.ncbi.nlm.nih.gov/24422520
https://pubmed.ncbi.nlm.nih.gov/24422520
Publikováno v:
Australian Journal of Chemistry. 68:1221
This research paper describes a second-generation, enantioselective synthesis of (+)-GR24. This new strategy circumvents the need for ozonolysis, which may not be suitable for reactions performed on scale. This flexible new approach is then used to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1dd2d0f3134b729579f4c581adc8849
https://doi.org/10.1071/ch15298
https://doi.org/10.1071/ch15298