1219981-72-2Relevant academic research and scientific papers
A unified total synthesis of aspergillides A and B
Fuwa, Haruhiko,Yamaguchi, Hiroshi,Sasaki, Makoto
supporting information; experimental part, p. 1848 - 1851 (2010/09/16)
An enantioselective total synthesis of aspergillides A and B has been accomplished based on a unified strategy, wherein a hydroxy-directed, highly chemoselective olefin cross-metathesis and a diastereoselective intramolecular oxa-conjugate cyclization were employed to forge the 2,6-substituted tetrahydropyran substructure.
An enantioselective total synthesis of aspergillides A and B
Fuwa, Haruhiko,Yamaguchi, Hiroshi,Sasaki, Makoto
experimental part, p. 7492 - 7503 (2010/12/19)
An enantioselective total synthesis of aspergillides A and B has been accomplished on the basis of a unified synthetic strategy that exploits stereodivergent intramolecular oxa-conjugate cyclization and Yamaguchi macrolactonization.
