862603-26-7Relevant academic research and scientific papers
Stereoselective synthesis of cis-2,5-disubstituted THFs: Application to adjacent bis-THF cores of annonaceous acetogenins
Fujioka, Hiromichi,Maehata, Ryota,Wakamatsu, Shintaro,Nakahara, Kenji,Hayashi, Tatsuya,Oki, Tomohiro
supporting information; experimental part, p. 1054 - 1057 (2012/04/10)
The iodocyclization of γ,δ-unsaturated alcohols in the presence of a silyl enol ether produced cis-2,5-disubstituted tetrahydrofurans in one pot via siloxy intermediates. N-Iodosuccinimide (NIS) effectively worked as an activator of the double bonds in th
Stereoselective syntheses of rolliniastatin 1, rollimembrin, and membranacin
Keum, Gyochang,Hwang, Cheol Hee,Kang, Soon Bang,Kim, Youseung,Lee, Eun
, p. 10396 - 10399 (2007/10/03)
A radical cyclization of β-alkoxyvinyl sulfoxides-Pummerer rearrangement-allylation protocol was successfully applied to the synthesis of the threol cis/threol cis/erythro bis-oxolane moiety in rolliniastatin 1 (1), rollimembrin (2), and membranacin (3).
Total synthesis of (+)-rolliniastatin 1
Koert
, p. 2517 - 2520 (2007/10/02)
The first total synthesis of the naturally occurring acetogenin (+)-rolliniastatin 1 (1) has been achieved. A high degree of stereochemical control in the construction of the bis-THF system was accomplished by chelation controlled addition of functionalized organo-metallic reagents derived from 5 and 11 to α-alkoxy-aldehydes.
