57702-56-4Relevant 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 (2007/10/03)
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.
A Convenient Synthesis of 2-Cyclopentenone
Takano, Seiichi,Iwabuchi, Yoshiharu,Takahashi, Michiyasu,Ogasawara, Kunio
, p. 3445 - 3446 (2007/10/02)
A convenient and practical synthesis of 2-cyclopentenone has been developed.Keywords - 2-cyclopentenone; 4-tert-butoxy-2-cyclopentenol; 4-cumyloxy-2-cyclopentenol; dehydration