Tetrahedron letters

Preparation and alkylation of cyclic β-trimethylstannyl α, β-unsaturated esters. A new, general annulation sequence

E Piers, LAT Hoi

Index: Piers, Edward; Tse, Hoi Lun Allan Tetrahedron Letters, 1984 , vol. 25, # 30 p. 3155 - 3158

Full Text: HTML

Citation Number: 44

Abstract

Abstract The key steps of a newly developed annulation method involve (a) reaction of cyclic β-trifluoromethanesulfonyloxy α, β-unsaturated esters (eg 14–16) with lithium (phenylthio)( trimethylstannyl) cuprate,(b) alkylation of the resultant products (eg 17–19) with 1, ω-

Ring opening of cyclopropylketones induced by photochemical electron transfer

[Cossy, Janine; Furet, Nathalie; BouzBouz, Samir Tetrahedron, 1995 , vol. 51, # 43 p. 11751 - 11764]

Total synthesis of amphilectane-type diterpenoids:(±)-8, 15-diisocyano-11 (20)-amphilectene

[Piers; Llinas-Brunet; Oballa Canadian Journal of Chemistry, 1993 , vol. 71, # 9 p. 1484 - 1494]

Preparation and alkylation of cyclic β-trimethylstannyl α, β-unsaturated esters. A new, general annulation sequence

Abstract

Related Articles:

More Articles...