Issue 38, 2013
From the journal:

Chemical Communications

Conformationally restricted functionalized heteroaromatics: a direct access to novel indoloindoles via Pd-mediated reaction†

Bagineni Prasad,a   B. Yogi Sreenivas,a   D. Rambabu,a   G. Rama Krishna,b   C. Malla Reddy,b   K. Lalith Kumara  and  Manojit Pal*a  

* Corresponding authors

a Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India
E-mail: manojitpal@rediffmail.com
Tel: +91 40 6657 1500

b Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, West Bengal 741252, India

Abstract

A new, versatile and direct Pd-mediated method involving intramolecular cyclization of N-(2-iodoaryl)-N-(1-alkyl-1H-indol-2-yl)alkane/arene/heteroarene sulfonamide has been developed leading to a diverse and unique class of indolo[2,3-b]indoles for the potential inhibition of sirtuins.

Graphical abstract: Conformationally restricted functionalized heteroaromatics: a direct access to novel indoloindoles via Pd-mediated reaction

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Article information

DOI
https://doi.org/10.1039/C2CC38342J
Article type
Communication
Submitted
20 Nov 2012
Accepted
03 Jan 2013
First published
03 Jan 2013

Chem. Commun., 2013,49, 3970-3972

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Conformationally restricted functionalized heteroaromatics: a direct access to novel indoloindoles via Pd-mediated reaction

B. Prasad, B. Y. Sreenivas, D. Rambabu, G. R. Krishna, C. Malla Reddy, K. L. Kumar and M. Pal, Chem. Commun., 2013, 49, 3970 DOI: 10.1039/C2CC38342J

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