Article ID Journal Published Year Pages File Type
5224502 Tetrahedron 2010 8 Pages PDF
Abstract

A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic 14-membered macrolide neopeltolide has been achieved via two Prins cyclizations.

Graphical abstractDownload full-size image

Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization
Authors
, , ,