Issue 37, 2014

Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

Abstract

A novel Lewis acid catalyzed Prins/pinacol cascade process has been developed for the synthesis of 7-substituted-8-oxaspiro[4.5]decan-1-ones in good yields with excellent selectivity. This is the first example of the synthesis of oxaspirocycles from aldehydes and 1-(4-hydroxybut-1-en-2-yl)cyclobutanol through a cascade of Prins/pinacol rearrangement. This method is applicable to a wide range of aldehydes such as aromatic, aliphatic, heteroaromatic, and α,β-unsaturated aldehydes.

Graphical abstract: Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

Supplementary files

Article information

Article type
Paper
Submitted
09 Jun 2014
Accepted
28 Jul 2014
First published
28 Jul 2014

Org. Biomol. Chem., 2014,12, 7257-7260

Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

B. V. Subba Reddy, S. Gopal Reddy, M. Ramana Reddy, M. Pal Bhadra and A. V. S. Sarma, Org. Biomol. Chem., 2014, 12, 7257 DOI: 10.1039/C4OB01188K

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