114298-66-7Relevant articles and documents
AN APPROACH TO FORSKOLIN AN EFFICIENT SYNTHESIS OF A TRICYCLIC LACTONE INTERMEDIATE
Li, Tsung-Tee,Wu, Yu-Lin
, p. 4039 - 4040 (1988)
Tricyclic lactone l0, a potential intermediate for the synthesis of forskolin, was prepared from (+/-)-3-hydroxycyclocitral employing an intramolecular Michael addition as the key step.
Enantioselective synthesis of 1(R)-hydroxypolygodial
Della Monica, Carmela,Della Sala, Giorgio,D'Urso, Deborah,Izzo, Irene,Spinella, Aldo
, p. 4061 - 4063 (2005)
Enantioselective preparation of 1(R)-hydroxypolygodial (5) has been achieved starting from α-ionone through a synthetic strategy involving a Corey-Bakshi-Shibata oxazaborolidine-mediated reduction and a stereoselective Diels-Alder reaction as key steps.
Total Synthesis of (+/-)-Forskolin
Corey, E. J.,Jardina, Paul Da Silva,Rohloff, John C.
, p. 3672 - 3673 (2007/10/02)
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