Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281260 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The stereoselective synthesis of an advanced intermediate of Taxuspine U and X has been accomplished using a ring closing metathesis strategy. The feasibility of ring closing metathesis in synthesizing highly constrained and functionalized macrocycles has been demonstrated provided the appropriate substrate structure and substitution pattern are chosen.
Graphical abstractThe stereoselective synthesis of an advanced intermediate en route to Taxuspine U and X has been accomplished using a ring closing metathesis strategy.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Elena Galletti, Stanislava I. Avramova, Michela L. Renzulli, Federico Corelli, Maurizio Botta,