Issue 31, 2014

Total synthesis of (+)-monocerin via tandem dihydroxylation-SN2 cyclization and a copper mediated tandem cyanation–lactonization approach

Abstract

A simple and novel synthesis of (+)-monocerin was achieved in 15 steps and 15.5% overall yield from 3-buten-1-ol employing hydrolytic kinetic resolution, Julia olefination, intramolecular tandem Sharpless asymmetric dihydroxylation-SN2 cyclization and a novel copper mediated tandem cyanation–cyclization as the key steps.

Graphical abstract: Total synthesis of (+)-monocerin via tandem dihydroxylation-SN2 cyclization and a copper mediated tandem cyanation–lactonization approach

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2014
Accepted
29 May 2014
First published
29 May 2014

Org. Biomol. Chem., 2014,12, 5973-5980

Author version available

Total synthesis of (+)-monocerin via tandem dihydroxylation-SN2 cyclization and a copper mediated tandem cyanation–lactonization approach

U. Nookaraju, E. Begari and P. Kumar, Org. Biomol. Chem., 2014, 12, 5973 DOI: 10.1039/C4OB00965G

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