Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Valentin Soulard"'
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
The Wnt-pathway has a critical role in development and tissue homeostasis and has attracted increased attention to develop anticancer drugs due to its aberrant activation in many cancers. In this study, we identified a novel small molecule series wit
Externí odkaz:
https://doaj.org/article/1e0f46bf8217440aaeb16566fa049e38
Autor:
Emy André‐Joyaux, Lars Gnägi, Manuel Gnägi‐Lux, Camilo Andrés Melendez Becerra, Valentin Soulard, Nicholas D. C. Tappin, Philippe Renaud
Publikováno v:
PATAI'S Chemistry of Functional Groups. :1-102
Publikováno v:
Journal of the American Chemical Society. 140:155-158
Selective incorporation of deuterium atoms into molecules is of high interest for labeling purposes and for optimizing properties of drug candidates. A mild and environmentally benign method for the deuteration of alkyl iodides via radical pathway us
Autor:
Valentin Soulard, Dirk Trauner
Publikováno v:
Synfacts. 17:0096
Autor:
Valentin Soulard, Dirk Trauner
Publikováno v:
Synfacts. 16:1481
Autor:
Valentin Soulard, Dirk Trauner
Publikováno v:
Synfacts. 16:1225
Autor:
Dirk Trauner, Valentin Soulard
Publikováno v:
Synfacts. 16:1227
Autor:
Valentin Soulard, Dirk Trauner
Publikováno v:
Synfacts. 16:1105
Publikováno v:
Journal of the American Chemical Society. 140(1)
Selective incorporation of deuterium atoms into molecules is of high interest for labeling purposes and for optimizing properties of drug candidates. A mild and environmentally benign method for the deuteration of alkyl iodides via radical pathway us
Publikováno v:
Soulard, Valentin; Dénès, Fabrice; Renaud, Philippe (2016). Effect of Brønsted acids on the thiophenol-mediated radical addition–translocation–cyclization process for the preparation of pyrrolidine derivatives. Free radical research, 50(S1), S2-S5. Taylor & Francis 10.1080/10715762.2016.1223294
Free Radical Research
Free Radical Research, 2016, 50 (1), pp.S2-S5. ⟨10.1080/10715762.2016.1223294⟩
Free Radical Research
Free Radical Research, 2016, 50 (1), pp.S2-S5. ⟨10.1080/10715762.2016.1223294⟩
A thiophenol-mediated method for the conversion of propargylamines to pyrrolidines under acidic conditions is described. This cascade reaction involves addition of a thiyl radical to the terminal alkyne followed by a 1,5-hydrogen transfer (radical tr