146060-35-7Relevant academic research and scientific papers
Diethylzinc-mediated addition of 2,2-dibromo-2-fluoroacetamides to carbonyl compounds: Synthesis of α-bromo-α-fluoro-β-hydroxy amides and/or (Z)-fluorovinyl amides
Lemonnier, Gerald,Poisson, Thomas,Couve-Bonnaire, Samuel,Jubault, Philippe,Pannecoucke, Xavier
, p. 3278 - 3289 (2013)
We describe straightforward routes either to α-bromo-α-fluoro- β-hydroxy amides or to (Z)-α-fluoroacrylamides starting from aldehydes, ketones or imine and 2,2-dibromo-2-fluoroacetamides. Depending on the nature of the amide, these diethylzinc-mediated additions to aldehydes, ketones or imine afford selective access either to bromofluorohydrins or to (Z)-α-fluoroacrylamides. The corresponding products were obtained in moderate to very good yields and the configurations of both products were confirmed by X-ray analyses. Reactions between aldehydes, ketones or imines and 2,2-dibromo-2-fluoroacetamides, a new class of fluorinated reagent, allow straightforward selective access to α-bromo-α-fluoro-β-hydroxy amides and/or (Z)-α-fluoroacrylamides with moderate to excellent yields. Copyright
Synthesis of 1-Fluoro-2-Phenylvinyl Piperidino Ketones
Shen, Yanchang,Zhou, Yuefen
, p. 3081 - 3084 (2007/10/02)
A new palladium-catalysed synthesis of 1-fluoro-2-phenylvinyl piperidino ketones is described.
