Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Estela Espinos Ferri"'
Autor:
James S. Sharley, Guido Gambacorta, Ana María Collado Pérez, Estela Espinos Ferri, Amadeo Fernandez Miranda, Jorge Sanchez Quesada, Ian R. Baxendale
Publikováno v:
Data in Brief, Vol 46, Iss , Pp 108801- (2023)
The dataset of spectroscopic analysis performed on starting materials, intermediates, and products relating to the synthesis of Hedione are hereby presented. The data were acquired in Durham university during the period between October 2020 and Septe
Externí odkaz:
https://doaj.org/article/5fac70a1c969488285f4faa8560f31e2
Autor:
James S. Sharley, Guido Gambacorta, Ana María Collado Pérez, Estela Espinos Ferri, Amadeo Fernandez Miranda, Jorge Sanchez Quesada, Ian R. Baxendale
Publikováno v:
Tetrahedron, 2022, Vol.126, pp.133058 [Peer Reviewed Journal]
Nitro alkanes are valuable starting materials for functionalisation via their corresponding anions as well as their transformation into other important groups such as ketones via the Nef reaction. Herein, we report a process development study for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c33cc4aed313f9859c4b14104d7e53a6
http://dro.dur.ac.uk/37497/
http://dro.dur.ac.uk/37497/
Autor:
James S. Sharley, Guido Gambacorta, Ana María Collado Pérez, Estela Espinos Ferri, Amadeo Fernandez Miranda, Isabelle Fernández Fernández, Jorge Sanchez Quesada, Ian R. Baxendale
Publikováno v:
Tetrahedron, 2022, Vol.126, pp.133068 [Peer Reviewed Journal]
A new method for the oxidation of Hedione 1 to dehydrohedione 2, a high value intermediate in the flavour and fragrance industry, has developed based upon one pot α-chlorination-elimination sequence which can be readily scaled. The spontaneous elimi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e251295518a0c23c0ab254fc9275d22e
https://doi.org/10.2139/ssrn.4187023
https://doi.org/10.2139/ssrn.4187023
Autor:
James S. Sharley, Ian R. Baxendale, Ana Maria Collado Perez, Amadeo Fernandez Miranda, Estela Espinos Ferri
Publikováno v:
ChemInform. 47
A protocol for effecting a rapid Saegusa-type oxidation of enol acetates is reported. This new method relies on the in situ elimination of an α-bromo intermediate to generate α,β-unsaturated ketones using copper(II) bromide. The methodology develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e9d1794d401d057859d37e14e80581
https://doi.org/10.1002/chin.201638042
https://doi.org/10.1002/chin.201638042