Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Steven H. Bennett"'
Autor:
Changcheng Jing, Shahida Mallah, Ella Kriemen, Steven H. Bennett, Valerio Fasano, Alastair J. J. Lennox, Ingeborg Hers, Varinder K. Aggarwal
Publikováno v:
ACS Central Science, Vol 6, Iss 6, Pp 995-1000 (2020)
Externí odkaz:
https://doaj.org/article/2b3908695373437cbc6460d721595eea
Autor:
Steven H. Bennett, Jacob S. Bestwick, Vera P. Demertzidou, David J. Jones, Helen E. Jones, François Richard, Joshua A. Homer, Rosie Street-Jeakings, Andrew F. Tiberia, Andrew L. Lawrence
The stereoselective synthesis of chiral molecules in enantioenriched form – i.e., asymmetric synthesis – underpins many fields of pure and applied science. Enantioconvergent reactions are preeminent in contemporary asymmetric synthesis as they co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb0411d7f3ebb39cda496794d9c90e9
https://doi.org/10.26434/chemrxiv-2023-07jvx
https://doi.org/10.26434/chemrxiv-2023-07jvx
Autor:
Steven H. Bennett
Publikováno v:
Organic Syntheses. 99:139-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0ab096c3e03d12e05c10197ae4dd0be
https://doi.org/10.15227/orgsyn.099.0139
https://doi.org/10.15227/orgsyn.099.0139
Autor:
Varinder K. Aggarwal, Shahida Mallah, Valerio Fasano, Ella Kriemen, Ingeborg Hers, Steven H. Bennett, Changcheng Jing, Alastair J. J. Lennox
Publikováno v:
ACS Central Science, Vol 6, Iss 6, Pp 995-1000 (2020)
Jing, C, Mallah, S, Kriemen, E, Bennett, S H, Fasano, V, Lennox, A J J, Hers, I & Aggarwal, V K 2020, ' Synthesis, Stability, and Biological Studies of Fluorinated Analogues of Thromboxane A2 ', ACS Central Science, vol. 6, no. 6, pp. 995–1000 . https://doi.org/10.1021/acscentsci.0c00310
Jing, C, Mallah, S, Kriemen, E, Bennett, S H, Fasano, V, Lennox, A J J, Hers, I & Aggarwal, V K 2020, ' Synthesis, Stability, and Biological Studies of Fluorinated Analogues of Thromboxane A2 ', ACS Central Science, vol. 6, no. 6, pp. 995–1000 . https://doi.org/10.1021/acscentsci.0c00310
Platelet activation results in the generation of thromboxane A2 (TxA2), which promotes thrombus formation by further amplifying platelet function, as well as causing vasoconstriction. Due to its role in thrombus formation and cardiovascular disease,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9a9d1fa6c95aaea7a62181f963fdf6
https://doaj.org/article/2b3908695373437cbc6460d721595eea
https://doaj.org/article/2b3908695373437cbc6460d721595eea
Autor:
Alexander Fawcett, Elliott H Denton, Tobias Biberger, Varinder K. Aggarwal, Valerio Fasano, Steven H. Bennett, Nils Winter
Publikováno v:
Bennett, S, Fawcett, A, Denton, E, Biberger, T, Fasano, V, Winter, N & Aggarwal, V K 2020, ' Difunctionalization of C–C σ Bonds Enabled by the Reaction of Bicyclo[1.1.0]butyl Boronate Complexes with Electrophiles : Reaction Development, Scope, and Stereochemical Origins ', Journal of the American Chemical Society, vol. 142, no. 39, pp. 16766–16775 . https://doi.org/10.1021/jacs.0c07357
Journal of the American Chemical Society
Journal of the American Chemical Society
Difunctionalization reactions of C-C σ bonds have the potential to streamline access to molecules that would otherwise be difficult to prepare. However, the development of such reactions is challenging because C-C σ bonds are typically unreactive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a167d9e821c4dfd1da568c1b50f8ae7
https://pubmed.ncbi.nlm.nih.gov/32885974
https://pubmed.ncbi.nlm.nih.gov/32885974
Publikováno v:
Bennett, S H, Coulthard, G & Aggarwal, V K 2020, ' Prostaglandin Total Synthesis Enabled by the Organocatalytic Dimerization of Succinaldehyde ', Chemical Record . https://doi.org/10.1002/tcr.202000054
Prostaglandins have been attractive targets in total synthesis for over 50 years, resulting in the development of new synthetic strategies and methodologies that have served the broader chemical community. However, these molecules are not just of aca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd5618c5f1b90c3aec47cf204afb9dbb
https://hdl.handle.net/1983/227d0a3b-8544-458c-9791-a6a59a63e6cf
https://hdl.handle.net/1983/227d0a3b-8544-458c-9791-a6a59a63e6cf
A chemoselective tandem reaction of a multi-reactive, two electrophile + two nucleophile, system is reported. An allylation/cross-coupling process of a haloaryl aldehyde, an aryl BPin, and an allyl BPin can be controlled using a temperature gradient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2331a182264630eb938215cc13b6c4e3
https://strathprints.strath.ac.uk/61783/1/Xu_etal_CC_2017_A_one_pot_tandem_chemoselective_allylation_cross_coupling.pdf
https://strathprints.strath.ac.uk/61783/1/Xu_etal_CC_2017_A_one_pot_tandem_chemoselective_allylation_cross_coupling.pdf