128372-48-5Relevant articles and documents
Formal [4 + 1]- and [5 + 1]-annulation by an SN2-conjugate addition sequence: Stereoselective synthesis of highly substituted carbocycles
Tong, Benny Meng Kiat,Chen, Hui,Chong, Sin Yee,Heng, Yi Li,Chiba, Shunsuke
supporting information; experimental part, p. 2826 - 2829 (2012/08/07)
K2CO3-mediated reactions of 6-bromo-2-hexenoates and 7-bromo-2-heptenoate with active methylene compounds deliver highly substituted cyclopentane and cyclohexane derivatives, respectively via a sequence of S N2-conjugate a
A FACILE SYNTHESIS OF 4-ARYLBUTYROLACTONES VIA THE PALLADIUM-CATALYZED ARYLATION OF 1,3-DIOXEP-5-ENE
Sakamoto, Takao,Kondo, Yoshinori,Yamanaka, Hiroshi
, p. 2437 - 2440 (2007/10/02)
1,3-Dioxep-5-ene was arylated by using Heck reaction, and the arylated 1,3-dioxep-5-ene derivatives were easily converted into 4-arylbutyrolactones, intermediates for the synthesis of natural products and biological active compounds.