Issue 13, 2011
From the journal:

Chemical Communications

Facile synthesis of diiodinated dihydronaphthalenes and naphthalenesviaiodine mediated electrophilic cyclization†

Fan Yang,a   Tienan Jin,*ab   Ming Baoc  and  Yoshinori Yamamoto*ab  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8548, Japan
E-mail: tjin@m.tohoku.ac.jp, yoshi@m.tohoku.ac.jp
Fax: +81 22-795-6784
Tel: +81 22-795-6581

b WPI-AIMR (WPI-Advanced Institute for Materials Research), Tohoku University, Sendai 980-8577, Japan

c State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012, China

Abstract

A facile, efficient, and general synthetic method for a wide range of 2,3-diiodinated 1,4-dihydrothiophenes and naphthalenes has been developed via the electrophilic iodocyclization of various aryl propargyl alcohols. The resulting product 2p can be used for the synthesis of a rubrene intermediate.

Graphical abstract: Facile synthesis of diiodinated dihydronaphthalenes and naphthalenesviaiodine mediated electrophilic cyclization

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC05442A
Article type
Communication
Submitted
08 Dec 2010
Accepted
07 Feb 2011
First published
21 Feb 2011

Chem. Commun., 2011,47, 4013-4015

Permissions

Request permissions

Facile synthesis of diiodinated dihydronaphthalenes and naphthalenesviaiodine mediated electrophilic cyclization

F. Yang, T. Jin, M. Bao and Y. Yamamoto, Chem. Commun., 2011, 47, 4013 DOI: 10.1039/C0CC05442A

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