Total Synthesis of Crotophorbolone

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  • Published: 06 July 2020
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
  • Source / Publisher: Chemical Science/Royal Society of Chemistry
  • Associated Societies: Royal Society of Chemistry (RSC), UK
thumbnail image: Total Synthesis of Crotophorbolone

Crotophorbolone (pictured) is a diterpenoid natural product. It belongs to a family of diterpenoids that includes, for example, phorbol and prostratin. These compounds have interesting biological activities and tricyclic frameworks with multiple stereogenic centers. Crotophorbolone has a trans,trans-5/7/6 tricyclic ring system with six contiguous stereogenic centers, which is challenging to synthesize. The first total synthesis of crotophorbolone was achieved in 2015 [1] and required thirty-four linear steps.

Bo Liu and colleagues, Sichuan University, China, have performed an eighteen-step total synthesis of crotophorbolone using a convergent strategy. The team started from (−)-carvone and [+]dimethyl-2,3-O-isopropylidene-L-tartrate. Carvone was used as the basis for the six-membered ring and subjected to a diastereoselective hydroxylation and a vinylation. The tartrate was converted to the five-membered-ring fragment via a methallylation and an intramolecular aldol condensation.

The five-ring fragment was converted to an alkenyl lithium intermediate and coupled with the six-ring fragment in the presence of CeCl3. Ring-closing metathesis (RCM) was used to close the central seven-membered ring and give the desired 5/7/6 tricyclic skeleton. The synthesis was concluded by the selective introduction of hydroxyl groups to obtain crotophorbolone.






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