4.4 Article

Total synthesis of (S)-(-)-curvularin:: A ring-closing-metathesis-based construction of the macrocyclic framework

Journal

SYNLETT
Volume -, Issue 12, Pages 1801-1804

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2008-1078504

Keywords

curvularin; cytotoxic; ring-closing metathesis; Pinnick oxidation; Wittig reaction

Ask authors/readers for more resources

A convergent, flexible, and efficient approach to the synthesis of curvularin is described. Key step is the high-yielding macrocyclic ring formation by ring-closing metathesis (RCM) using the Grubbs second-generation catalyst.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available