Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Simon, T. R."'
Autor:
Santi, Micol1, Müller, Simon T. R.1, Folgueiras‐Amador, Ana A.1, Uttry, Alexander1, Hellier, Paul2, Wirth, Thomas1 wirth@cf.ac.uk
Publikováno v:
European Journal of Organic Chemistry. 4/10/2017, Vol. 2017 Issue 14, p1889-1893. 5p. 1 Color Photograph, 5 Diagrams, 3 Charts.
Autor:
Alexander Uttry, Paul Hellier, Thomas Wirth, Micol Santi, Ana A. Folgueiras-Amador, Simon T. R. Müller
Publikováno v:
European Journal of Organic Chemistry. 2017:1889-1893
A stereoselective synthesis of 2,3-dihydro-1H-indoles with a RhII-catalyzed C–H insertion is reported. The α-diazo carbonyl intermediates can be obtained by a diazo-transfer reaction of 2-aminophenylacetic acids. Optimization and kinetic studies w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad9e52f204b329d47aeb4506a21b8654
https://doi.org/10.1002/ejoc.201700412
https://doi.org/10.1002/ejoc.201700412
Publikováno v:
Monatshefte Fur Chemie
Four new metal complexes [Cu(ISO)2], [Cu(BUT)2] and [Zn(ISO)2], [Zn(BUT)2] of the polyhydroxychalcones (isoliquiritigenin and butein) are synthesized, structurally characterized and their antioxidant activity is investigated. The formation of the com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bca04d265639ea3af809db5eb008d7a7
https://doi.org/10.1007/s00706-016-1822-7
https://doi.org/10.1007/s00706-016-1822-7
Autor:
Müller, Simon T. R.1, Murat, Aurélien2, Maillos, Delphine2, Lesimple, Patrick2, Hellier, Paul2, Wirth, Thomas1 wirth@cf.ac.uk
Publikováno v:
Chemistry - A European Journal. May2015, Vol. 21 Issue 19, p7016-7020. 5p.
Publikováno v:
Organic Process Research & Development. 20:495-502
The safe use of diazo reagents for the preparation of a key structure in the synthesis of milnacipran analogues is described herein. Using continuous flow technology, the diazo reagent is synthesized, purified, dried, and subsequently used in semi-ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2937c836d2efb01c52453435f08c6889
https://doi.org/10.1021/acs.oprd.5b00308
https://doi.org/10.1021/acs.oprd.5b00308
Autor:
Santi, Micol, Müller, Simon T. R., Folgueiras-Amador, Ana, Uttry, Alexander, Hellier, Paul, Wirth, Thomas
A stereoselective synthesis of 2,3-dihydro-1H-indoles with a RhII-catalyzed C–H insertion is reported. The α-diazo carbonyl intermediates can be obtained by a diazo-transfer reaction of 2-aminophenylacetic acids. Optimization and kinetic studies w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::a0079710b8762c827213abe7b1080347
https://orca.cardiff.ac.uk/id/eprint/99482/1/accepted_article.pdf
https://orca.cardiff.ac.uk/id/eprint/99482/1/accepted_article.pdf
Autor:
Simon T. R. Müller, Thomas Wirth
Publikováno v:
ChemSusChem. 8:245-250
Diazo compounds are very versatile reagents in organic chemistry and meet the challenge of selective assembly of structurally complex molecules. Their leaving group is dinitrogen; therefore, they are very clean and atom-efficient reagents. However, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1154258d710afa06c6fc3c4274b71f1
https://doi.org/10.1002/cssc.201402874
https://doi.org/10.1002/cssc.201402874
Publikováno v:
Synlett. 25:871-875
A safe and fast method for the production of β-hydroxy-α-diazoesters in continuous flow technology is described. The synthesis involves the formation of ethyl diazoacetate in situ and the addition to several aldehydes in a two-step continuous flow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d6017822145d929500abcd46bd2872e
https://doi.org/10.1055/s-0033-1340835
https://doi.org/10.1055/s-0033-1340835
Autor:
Müller, Simon T. R.1, Hokamp, Tobias1, Ehrmann, Svenja1, Hellier, Paul2, Wirth, Thomas1 wirth@cf.ac.uk
Publikováno v:
Chemistry - A European Journal. 8/16/2016, Vol. 22 Issue 34, p11940-11942. 3p.
Publikováno v:
Scientific American, 1978 Mar 01. 238(3), 10-17.
Externí odkaz:
https://www.jstor.org/stable/24955649