Of perezone

While the chirality of perezone (552) has been known for some time that of the a- (555) and p-pipitzols (554) which are derivable from 552 by thermolysis was rigorously proven only recently by chemical transformation to cedrene and x-ray diffraction The cycliration of 552 has been shown to involve a ncerted [4+2] cycloaddition which lacks stereochemical induction by the chiral center already present, since 555 and 554 are obtained in equimolar amounts However, a stepwise mechanism having higher stereoselectivity is followed by 552 in the presence... 

On thermolysis, perezone (192) undergoes a [4+2] cycloaddition to produce equal amounts of the two pipitzols (193) and (194) i.e. there is no stereochemical induction by the chiral centre in (192). If, however, the reaction is carried at 0 °C in the presence of boron trifluoride etherate the cyclization becomes highly stereoselective producing largely a-pipitzol (193) and it has been shown that a stepwise mechanism (195)—K196)->(193) is operative in this case.108... 

New bisabolane sesquiterpenoids include (59), (60)/ and the perezone derivatives (61)—(63). Based on mass spectral evidence structures (64) and (65) have been assigned to two minor constituents of Chinese cinnamon oil both ketones have been synthesized from a-curcumene. Dihydroxydeodactol (66), a derivative of deodactol, has been isolated from the mollusc Aplysia dactylomela. A... 

Walls F, Padilla J, Joseph-Nathan P, Giral F, Escobar M, Romo J 1966 Studies in perezone derivatives, structures of the pipitzols and perezinone. Tetrahedron 22 2387-2399... 

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