4.4 Article

Total synthesis of atorvastatin via a late-stage, regioselective 1,3-dipolar munchnone cycloaddition

Journal

TETRAHEDRON LETTERS
Volume 56, Issue 23, Pages 3208-3211

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2014.12.104

Keywords

Munchnone; 1,3-Dipolar cycloaddition; Atorvastatin; Pyrrole; Mesoionic

Ask authors/readers for more resources

Atorvastatin was prepared in seven steps from commercially available 4-fluorophenylacetic acid. The key 1,3-dipolar cycloaddition was conducted regioselectively using a complex munchnone which was prepared in five steps on decagram scale. (C) 2015 Elsevier Ltd. All rights reserved.

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