258834-26-3Relevant articles and documents
Lipase-mediated resolution of cis-4-cumyloxy-2-cyclopenten-1-ol and its utilization for enantioconvergent preparation of (-)-oxabicyclo[3.3.0]oct-6- en-3-one
Nakashima, Hiromi,Sato, Masayuki,Taniguchi, Takahiko,Ogasawara, Kunio
, p. 1754 - 1756 (1999)
Convenient preparation of both enantiomers of cis-4-cumyloxy-2- cyclopenten-1-ol from cyclopentadiene employing a lipase-mediated resolution was first established. An efficient enantioconvergent transformation of both enantiomeric products affording (-)-oxabicyclo[3.3.0]oct-6-en-3-one, an important building block of prostaglandin synthesis, was next established.
Letter: A simple total synthesis of prostaglandins from 4-cumyloxy-2-cyclopentenone.
Stork,Isobe
, p. 6260 - 6261 (2007/10/14)
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