4.8 Article

A Macrocyclic Approach to Tetracycline Natural Products. Investigation of Transannular Alkylations and Michael Additions

Journal

ORGANIC LETTERS
Volume 14, Issue 23, Pages 5840-5843

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol302691j

Keywords

-

Funding

  1. National Institutes of Health [GM-33328-21, GM-081546-04]
  2. Swiss National Science Foundation
  3. Novartis Foundation
  4. DAAD

Ask authors/readers for more resources

A new approach to the tetracycline core structure is presented. The pivotal intermediate is identified as macrocycle III. The two interior bonds (C4a-C12a and C5a-C11a) are to be constructed through sequential transannular Michael additions (III-II) and compression-promoted transannular isoxazole alkylations from intermediate II.

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