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Hardwickia pinnata

Misra R, Pandey R C, Sukh Dev 1978 Higher isoprenoids. X. Diterpenoids from the oleoresin of Hardwickia pinnata. Part 3 Kolavenol, kolavelool and a nor diterpene hydrocarbon. Tetrahedron 35 985-987... [Pg.802]

Structural correlation of solidagonic acid with 495 and 475 was made feasible by the recent assignment by Misra and coworkers 391) of absolute stereochemistry to the chiral centers of the Hardwickia pinnata clerodanes, (-)-hardwickiic acid (511), kolavenic acid, and kolavenol (Figure 34 [p. 515]). Their pivotal work on clerodane stereochemistry proceeded as described below ... [Pg.493]

See other pages where Hardwickia pinnata is mentioned: [Pg.490]    [Pg.739]    [Pg.740]    [Pg.490]    [Pg.739]    [Pg.740]   
See also in sourсe #XX -- [ Pg.740 , Pg.752 ]

See also in sourсe #XX -- [ Pg.483 ]

See also in sourсe #XX -- [ Pg.493 ]



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