436153-70-7Relevant academic research and scientific papers
Divergent synthesis of trans-fused polycyclic ethers by a convergent oxiranyl anion strategy
Sakai, Takeo,Sugimoto, Ai,Tatematsu, Hiroki,Mori, Yuji
, p. 11177 - 11191 (2013/02/23)
Octacyclic polyethers that correspond to the CDEFGHIJ-ring system of yessotoxin as well as G-and/or I-ring-modified analogues were synthesized in a divergent manner, starting from a common intermediate, using an [X + 2 + Y]-type convergent method. Reaction of a triflate with the oxiranyl anion generated from an epoxy sulfone, followed by ring expansion, allowed for the incorporation of medium-sized ring ethers into the key intermediate. Subsequent acetal formation and reductive etherification afforded various octacycles containing seven-and eight-membered ether rings.
Studies toward the total synthesis of gymnocin A, a cytotoxic polyether: A highly convergent entry to the F-N ring fragment
Sasaki, Makoto,Tsukano, Chihiro,Tachibana, Kazuo
, p. 1747 - 1750 (2007/10/03)
Matrix presented An efficient and highly convergent synthesis of the FGHIJKLMN ring fragment of gymnocin A, a cyctotoxic polycyclic ether isolated from the notorious red-tide forming dinoflagellate Gymnodinium mikimotoi, has been achieved. The present syn
