Issue 2, 2012
From the journal:

Organic & Biomolecular Chemistry

Microwave-assisted benzyl-transfer reactions of commercially available 2-benzyloxy-1-methylpyridinium triflate†

Teng-wei Wang,‡a   Tanit Intaranukulkit,‡a   Michael R. Rosana,a   Rimantas Slegeris,a   Janet Simona  and  Gregory B. Dudley*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida, USA
E-mail: gdudley@chem.fsu.edu
Fax: +1-850-644-8281
Tel: +1-850-644-2333

Abstract

Benzylation of alcohols and other substrates under thermal conditions translates smoothly from conventional heating into MW-assisted organic synthesis (MAOS). Reactions times are decreased from hours to minutes while good to excellent yields are maintained. MW heating should be considered for benzylation of high-value substrates using the title reagent.

Graphical abstract: Microwave-assisted benzyl-transfer reactions of commercially available 2-benzyloxy-1-methylpyridinium triflate

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Article information

DOI
https://doi.org/10.1039/C1OB06504A
Article type
Communication
Submitted
02 Sep 2011
Accepted
10 Oct 2011
First published
13 Oct 2011

Org. Biomol. Chem., 2012,10, 248-250

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Microwave-assisted benzyl-transfer reactions of commercially available 2-benzyloxy-1-methylpyridinium triflate

T. Wang, T. Intaranukulkit, M. R. Rosana, R. Slegeris, J. Simon and G. B. Dudley, Org. Biomol. Chem., 2012, 10, 248 DOI: 10.1039/C1OB06504A

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