Issue 42, 2014

The first stereoselective total synthesis of neosemburin and isoneosemburin

Abstract

The Claisen rearrangement of sugar derived allyl vinyl ether, Wittig olefination and intramolecular acetalization reactions were used as key steps in the first stereoselective total synthesis of neosemburin and isoneosemburin through the formation of a 3-C-branched sugar precursor as a key intermediate.

Graphical abstract: The first stereoselective total synthesis of neosemburin and isoneosemburin

Supplementary files

Article information

Article type
Paper
Submitted
14 Jun 2014
Accepted
15 Jul 2014
First published
15 Jul 2014

Org. Biomol. Chem., 2014,12, 8408-8414

Author version available

The first stereoselective total synthesis of neosemburin and isoneosemburin

G. M. Reddy and P. R. Sridhar, Org. Biomol. Chem., 2014, 12, 8408 DOI: 10.1039/C4OB01239A

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