RE: ORGLIST: Deprotection of the indole N

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From: Peng Gao (pgao00$##$st.lzu.edu.cn)
Date: Wed May 17 2006 - 13:45:10 EDT

It's a good idea for constructing the indole ring last. In fact, deprotection is
the last step for the total synthesis of the target molecular. Constructing the
indole at the last step may cause a big modulate of my synthetic route. Maybe
there are other methods retaining my original route to solve this problem.
Thank you very much!

>From: "will jones" <willjones46$##$hotmail.com>
>Reply-To:
>To: everybody$##$orglist.net
>Subject: RE: ORGLIST: Deprotection of the indole N
>Date:Wed, 17 May 2006 14:53:34 +0000
>
>Could you not get around the whole problem by constructing the indole ring
> last? There are loads of ways to make an indol ring, or have you already
> gone down that synthetic pathway as well?
>

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