4.8 Article

Synthesis of Antimicrobial Natural Products Targeting FtsZ: (+)-Totarol and Related Totarane Diterpenes

Journal

ORGANIC LETTERS
Volume 12, Issue 15, Pages 3324-3327

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol100929z

Keywords

-

Funding

  1. UC Davis Academic Senate Committee
  2. NIH/NIAID [R56AI80931-01]
  3. United States Department of Education

Ask authors/readers for more resources

An efficient, convergent synthesis of totarol by a diastereoselective epoxide/alkene/arene bicyclization is described. The reported synthesis enables the preparation of related diterpenes totaradiol and totarolone as well as previously unavailable derivatives that exhibit comparable Inhibition of the bacterial cell division protein FtsZ.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available