89-89-4Relevant articles and documents
Enantioselective synthesis of (+)-α-vetivone through the Michael reaction of chiral imines
Revial, Gilbert,Jabin, Ivan,Pfau, Michel
, p. 4975 - 4983 (2007/10/03)
(+)-α-Vetivone has been synthesised in nine steps. The absolute stereochemistry of the two stereogenic centres is controlled in the same key step involving the stereoselective Michael addition of a chiral imine of 4-isopropylidene-2-methylcyclohexanone to phenyl crotonate.
Structure and absolute configuration of kusunol.
Hikino,Suzuki,Takemoto
, p. 832 - 838 (2007/10/05)
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