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The first stereoselective total synthesis of neosemburin and isoneosemburin†
Gadi Madhusudhan Reddy,Perali Ramu Sridhar
Organic & Biomolecular Chemistry Pub Date : 07/15/2014 00:00:00 , DOI:10.1039/C4OB01239A
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
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