Issue 8, 2006
From the journal:

Chemical Communications

Fluorous-tagged indolylboron for the diversity-oriented synthesis of biologically-attractive bisindole derivatives†

Takahiro Kasaharaa  and  Yoshinori Kondo*b  

* Corresponding authors

a Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki Aza Aoba 6-3, Aoba-ku, Sendai, Japan
E-mail: kasahara@mail2.pharm.tohoku.ac.jp
Fax: (+81) 22-795-5917
Tel: (+81) 22-795-5917

b Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki Aza Aoba 6-3, Aoba-ku, Sendai, Japan
E-mail: ykondo@mail.pharm.tohoku.ac.jp
Fax: (+81) 22-795-6804
Tel: (+81) 22-795-6804

Abstract

The diversity-oriented synthesis of bisindole derivatives to construct concise libraries using consecutive cross-coupling reactions and prepare new sulfonamide type fluorous protecting groups is presented.

Graphical abstract: Fluorous-tagged indolylboron for the diversity-oriented synthesis of biologically-attractive bisindole derivatives

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Article information

DOI
https://doi.org/10.1039/B516487G
Article type
Communication
Submitted
21 Nov 2005
Accepted
05 Jan 2006
First published
19 Jan 2006

Chem. Commun., 2006, 891-893

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Fluorous-tagged indolylboron for the diversity-oriented synthesis of biologically-attractive bisindole derivatives

T. Kasahara and Y. Kondo, Chem. Commun., 2006, 891 DOI: 10.1039/B516487G

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