Issue 6, 2006
From the journal:

Chemical Communications

Novel cyclization reaction of 1,ω-diiodo-1-alkynes without the loss of iodine atoms†

Toshiro Harada,*a   Kenta Mizunashia  and  Keiko Muramatsua  

* Corresponding authors

a Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, Japan
E-mail: harada@chem.kit.ac.jp
Fax: (+81) 75 724 7580
Tel: (+81) 75 724 7514

Abstract

In the presence of 1-hexynyllithium (0.2–0.6 equiv.), 1,ω-diiodo-1-alkynes undergo a new type of cyclization reaction without the loss of two iodine atoms to afford (diiodomethylene)cycloalkanes.

Graphical abstract: Novel cyclization reaction of 1,ω-diiodo-1-alkynes without the loss of iodine atoms

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B516515F
Article type
Communication
Submitted
22 Nov 2005
Accepted
08 Dec 2005
First published
06 Jan 2006

Chem. Commun., 2006, 638-639

Permissions

Request permissions

Novel cyclization reaction of 1,ω-diiodo-1-alkynes without the loss of iodine atoms

T. Harada, K. Mizunashi and K. Muramatsu, Chem. Commun., 2006, 638 DOI: 10.1039/B516515F

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