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Merck

Total synthesis of TAK-kinase inhibitor LL-Z1640-2 via consecutive macrocyclization and transannular aromatization.

Organic letters (2010-11-12)
Hideki Miyatake-Ondozabal, Anthony G M Barrett
ABSTRAKT

The biomimetic total synthesis of LL-Z1640-2 (3) is reported without the use of phenol protection. The aromatic unit was constructed via the transannular aromatization of macrocyclic triketo-ester 2, which in turn was synthesized by macrolactonization using an intramolecular trapping of a triketo-ketene derived from dioxinone 1.

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Sigma-Aldrich
1,3-Dioxolane, anhydrous, contains ~75 ppm BHT as inhibitor, 99.8%
Sigma-Aldrich
1,3-Dioxolane, ReagentPlus®, contains ~75 ppm BHT as inhibitor, 99%