Zhang J,
Li Z,
Zhuo J,
Cui Y,
Han T,
Li C.
* National Institute of Biological Sciences, Beijing, Tsinghua University, Beijing, Graduate School of Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, P. R. of China
Tandem Decarboxylative Cyclization/Alkenylation Strategy for Total Syntheses of (+)-Longirabdiol, (–)-Longirabdolactone, and (–)-Effusin.
J. Am. Chem. Soc. 2019;
141: 8372-8380
Key words
(+)-longirabdiol - (–)-longirabdolactone - (–)-effusin - radical cyclization - Giese reaction - Riley oxidation
Significance
Owing to their well-established biological effects and structural complexity, ent-kaurane diterpenoid natural products continue to attract interest from the synthetic community. Li and co-workers present enantioselective total syntheses of three spirolactone ent-kauranoids by relying on a sequence involving an elegant tandem decarboxylative cyclization alkenylation. Two additional free radical-based cyclization events allowed the team to access (+)-longirabdiol. Closely related natural products (–)-longirabdolactone and (–)-effusin were synthesized by implementation of few additional transformations.
Comment
The authors initiated their synthetic route by preparation of enantioenriched acid C followed by its subsequent transformation into the redox-active ester D. Tandem radical cyclization/alkenylation led to the formation of lactone F with good diastereoselectivity. Following functional group interconversions, intermolecular decarboxylative Giese reaction and intramolecular lactonization gave rise to spiro-compound I. This intermediate was transformed into advanced intermediate J, thereby setting the stage for the last radical cyclization, allylic oxidation, and desilylation to afford (+)-longirabdiol.
