Issue 47, 2011
From the journal:

Chemical Communications

A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane†

Saikat Khamarui,a   Deblina Sarkar,a   Palash Pandita  and  Dilip K. Maiti*a  

* Corresponding authors

a Department of Chemistry, University of Calcutta, University College of Science, 92, A. P. C. Road, Kolkata-700009, India
E-mail: dkmchem@caluniv.ac.in
Fax: +91-33-2351-9755
Tel: +91-33-2350-9937

Abstract

A general strategy for fast decarboxylative difunctionalization to gem-dihalohydrin, gem-dihaloether, gem-dibromoester and cyclized bromo-1,4-dioxane synthons with outstanding regio- and stereoselectivity is demonstrated.

Graphical abstract: A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane

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Article information

DOI
https://doi.org/10.1039/C1CC16126A
Article type
Communication
Submitted
01 Oct 2011
Accepted
21 Oct 2011
First published
31 Oct 2011

Chem. Commun., 2011,47, 12667-12669

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A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane

S. Khamarui, D. Sarkar, P. Pandit and D. K. Maiti, Chem. Commun., 2011, 47, 12667 DOI: 10.1039/C1CC16126A

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