From: will jones (willjones46$##$hotmail.com)
Date: Fri Oct 13 2006 - 10:01:15 EDT
You could get some hydrazine-terminated beads. That will form a hydrazone
bond with your product. Then you could probably elute off at low pH (2-3) as
the hydrazone is hydrolysed.
However, I don't know how strong aromatic hydrazone systems are. I reckon it
would definately work for an aliphatic.
If the bond won't hydrolyse, then use amine-terminated beads. There are
loads of different types around.
Will
>From: yogi anji <yogi_kasetti$##$yahoo.co.in>
>To: everybody$##$orglist.net
>Subject: ORGLIST: AROMATIC ETHER FORMATION
>Date: Thu, 12 Oct 2006 19:43:26 +0100 (BST)
>
>i have problem in getting product from starting material an alcohol as
>shown in the scheme given in the attachment.I kindly appreciate any
>suggestions for using appropriate reagents.
> Thank you.
>
> K.Yoganjaneyulu
> Department of medicinal chemistry
> National institue of pharmaceutical education and research
> punjab
> india
>
>
>---------------------------------
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