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Merck
CN
  • Improved procedure for the enantiometric synthesis of 1-hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicycl.

Improved procedure for the enantiometric synthesis of 1-hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicycl.

Bioscience, biotechnology, and biochemistry (2001-03-29)
F Ishibashi, M Hayashita, M Okazaki, Y Shuto
摘要

Short enantiomeric syntheses of the 1-hydroxy/acetoxy-3,7-dioxabicyclo[3.3.0]octane lignans, paulownin, and (+)-phrymarin I and II, were accomplished by starting from the chiral synthon, (R)-(+)-3-hydroxybutanolide, and employing photocyclization as the key step.

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Sigma-Aldrich
Paulownin, ≥95% (LC/MS-ELSD)