1,2-Addition of α,α,α-trichlorotoluene to ketones via a Mg Barbier reaction in DMF: New route to cycloalk-1-en-1-yl and alk-1-en-1-yl phenyl ketones
The reductive cyclocondensation of α,α,α-trichlorotoluene to enolisable ketones enables the preparation of (cyclo)alken-1-en-1-yl phenyl ketones via the formation of an intermediate chlorooxirane. Copyright Taylor & Francis Group, LLC.
Aaziz, Akima,Oudeyer, Sylvain,Leonel, Eric,Paugam, Jean Paul,Nedelec, Jean-Yves
p. 1147 - 1154
(2008/02/01)
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