Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Organic Chemistry Forum for Graduate Students and Professionals => Topic started by: 408 on September 17, 2013, 09:03:47 PM
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I have a rather electron poor heterocycle that I am building up. The easy synthetic route will leave it phenyl-substitued. The difficult route, benzyl substituted. Obviously benzyl is easy to remove. But what about phenyl? I have seen a couple hardcore dephenylations using stuff like sodium in liquid ammonia, but is there anything easier?
thanks,
408.
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p-methoxysubstituted phenyl can be removed with CAN :)