259198-96-4Relevant articles and documents
A novel approach to the CDE ring system of pectenotoxin-4 triggered by VO(acac)2-induced epoxy-acetalization
Carley, Sarah,Brimble, Margaret A.
supporting information; experimental part, p. 563 - 566 (2009/08/19)
(Chemical Equation Presented) A novel approach to the CDE fragment of pectenotoxin-4 is described wherein the bicyclic acetal is constructed via a cascade cyclization induced by VO(acac)2 epoxidation of a homoallylic 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.