4.8 Article

Atroposelective Heck Macrocyclization: Enantioselective Synthesis of Bis(bibenzylic) Natural Products

Journal

ORGANIC LETTERS
Volume 14, Issue 17, Pages 4548-4551

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol302132s

Keywords

-

Funding

  1. Deutsche Forschungsgemeinschaft [DFG Sp 498/2-1]

Ask authors/readers for more resources

The Heck protocol was applied for the first time to the atroposelective synthesis of macrocyclic natural products. As ring closure to bis(bibenzyls) of the isoplagiochin type leads to a configurationally stable biaryl axis in the molecule, cyclization could be conducted atroposelectively in the presence of a chiral BINAP ligand.

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