Issue 18, 2012
From the journal:

Organic & Biomolecular Chemistry

4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2]pyrrole†

K. C. Gowri Sreedevi,a   Ajesh P. Thomas,b   S. Ramakrishnan,a   P. S. Salini,a   M. G. Derry Holaday,a   M. L. P. Reddyc  and  A. Srinivasan*b  

* Corresponding authors

a Photosciences and Photonics Section, National Institute for Interdisciplinary Science and Technology (NIIST-CSIR), Trivandrum-695019, Kerala, India

b National Institute of Science Education and Research (NISER), Bhubaneswar-751005, Odisha, India
E-mail: srini@niser.ac.in

c Inorganic Chemistry Section, Chemical Sciences and Technology Division, National Institute for Interdisciplinary Science and Technology (NIIST-CSIR), Trivandrum-695019, Kerala, India

Abstract

Synthesis, spectral and structural characterization of a pyrroloindolizine derivative having structural similarity with calix[2]pyrrole is described. Here, two pyrrole rings are connected with two meso-carbon atoms having an N,α-linkage and an α,β-linkage to afford the smallest analogue in the calixpyrrole family. Detailed NMR spectroscopic studies along with single crystal X-ray analysis confirm the assigned structure of the molecule.

Graphical abstract: 4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2]pyrrole

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2OB25228G
Article type
Communication
Submitted
31 Jan 2012
Accepted
13 Mar 2012
First published
15 Mar 2012

Org. Biomol. Chem., 2012,10, 3600-3605

Permissions

Request permissions

4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2]pyrrole

K. C. G. Sreedevi, A. P. Thomas, S. Ramakrishnan, P. S. Salini, M. G. D. Holaday, M. L. P. Reddy and A. Srinivasan, Org. Biomol. Chem., 2012, 10, 3600 DOI: 10.1039/C2OB25228G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements