137046-97-0Relevant academic research and scientific papers
SYNTHETIC STUDIES ON PODOPHYLLUM LIGNANS: TRIBUTYLTIN HYDRIDE-INDUCED RADICAL CYCLIZATION AND INTRAMOLECULAR HECK REACTION OF α-BENZYLIDENE-β-(o-BROMOBENZYL)-γ-LACTONES
Ishibashi, Hiroyuki,Ito, Katsuhiro,Tabuchi, Masayo,Ikeda, Masazumi
, p. 1279 - 1282 (2007/10/02)
Tributyltin hydride-induced radical cyclization of the (Z)-α-benzylidene-β-(o-bromobenzyl)-γ-lactone (16) gave the 6-endo cyclization product, (+/-)-deoxyisopicropodophyllin (18), and the 5-exo cyclization product (19).On the other hand, the intramolecular Heck reaction of 16 provided (+/-)-γ-apopicropodophyllin (20) as a sole cyclization product.
