Issue 30, 2012

Enantioselective synthesis of C-linked spiroacetal-triazoles as privileged natural product-like scaffolds

Abstract

The enantioselective synthesis of novel C-linked spiroacetal-triazoles 10 is reported. The key step involves reaction of acetylenic spiroacetal 11 with several azides by the Copper-Catalysed AzideAlkyne Cycloaddition (CuAAC). The biologically privileged spiroacetal scaffold 11 was prepared from silyl-protected Weinreb amide 19 using several reliable Grignard additions and a highly diastereoselective enzymatic kinetic resolution.

Graphical abstract: Enantioselective synthesis of C-linked spiroacetal-triazoles as privileged natural product-like scaffolds

Supplementary files

Article information

Article type
Paper
Submitted
27 Հկտ 2011
Accepted
30 Նյմ 2011
First published
01 Դկտ 2011

Org. Biomol. Chem., 2012,10, 5993-6002

Enantioselective synthesis of C-linked spiroacetal-triazoles as privileged natural product-like scaffolds

J. T. B. Kueh, K. W. Choi and M. A. Brimble, Org. Biomol. Chem., 2012, 10, 5993 DOI: 10.1039/C2OB06802H

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