259199-01-4Relevant articles and documents
Total synthesis of (-)-laulimalide: Pd-catalyzed stereospecific ring construction of the substituted 3,6-dihydro[2H]pyran units
Uenishi, Jun'Ichi,Ohmi, Masashi
, p. 2756 - 2760 (2007/10/03)
(Chemical Equation Presented) The potent anticancer agent (-)-laulimalide (1) was prepared through a versatile method that should allow access to other marine natural products. Key steps included a Pd-catalyzed 1,3 chirality transfer of an allylic alcohol
Synthesis of the C1-C12-dihydropyran segment of the antitumor agent laulimalide by ring closing metathesis
Mulzer, Johann,Hanbauer, Martin
, p. 33 - 36 (2007/10/03)
A stereocontrolled synthesis of the C1-C12 fragment 3 of laulimalide utilizing a ring closing metathesis with Grubbs' catalyst as the key step is described.