256662-98-3Relevant articles and documents
Preparation of a synthetic equivalent of chiral methyl 2,5- dihydroxycyclohexane-1,4-dienecarboxylate
Yoshida, Naoyuki,Konno, Hiroyuki,Kamikubo, Takashi,Takahashi, Michiyasu,Ogasawara, Kunio
, p. 3849 - 3857 (1999)
A chiral tricyclic diol, serving as a synthetic equivalent of chiral methyl 2,5-dihydroxycyclohexane-1,4-dienecarboxylate, has been prepared in both enantiomeric forms by employing a lipase-mediated kinetic resolution in vinyl acetate.
Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative '(+)-parasitenone'. Identity of parasitenone with (+)-epoxydon
Mehta, Goverdhan,Pujar, Shashikant R.,Ramesh, Senaiar S.,Islam, Kabirul
, p. 3373 - 3376 (2007/10/03)
Short, simple and enantioselective syntheses of the natural product (+)-streptol, the non-peptide apoptosis inhibitor ent-RKTS-33 and the putative structure of 'parasitenone' have been accomplished from the readily available chiral building block. 'Parasi