Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles-Reference-Cited by-同舟云学术

Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles

Published:2015 Issue:48 Volume:5 Page:38075-38084
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Sarath Chand S.¹²³⁴⁵,Sasidhar B. S.¹²³⁴⁵,Prakash Praveen⁴⁵⁶³,Sasikumar P.⁴⁵⁶³,Preethanuj P.⁴⁵⁶³,Jaroschik Florian⁷⁸⁹,Harakat Dominique⁷⁸⁹,Vasse Jean-Luc⁷⁸⁹,Radhakrishnan K. V.¹²³⁴⁵

Affiliation:

1. Academy of Scientific and Innovative Research (AcSIR)

2. New Delhi 110001

3. India

4. Organic Chemistry Section

5. National Institute for Interdisciplinary Science and Technology (CSIR)

6. Trivandrum 695019

7. Université de Reims

8. 51687 Reims Cedex 2

9. France

Abstract

A Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles through the ring opening of pentafulvene derived diazabicyclic olefins has been developed toward the synthesis of indole and bisindole derivatives.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA01107H

Reference50 articles.

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