Metabolites produced by the Scleroderris canker fungus, Gremmeniellaabietina. Part 4. Biosynthetic studies

1987 ◽  
Vol 65 (4) ◽  
pp. 760-764 ◽  
Author(s):  
William A. Ayer ◽  
M. Soledade Pedras ◽  
Dale E. Ward

The biosynthetic origin of the carbon atoms of the most highly oxidized, polyketide derived, ring (carbons 1–3) of the Gremmeniellaabietina metabolites sclerodione (3), scleroderolide (4), sclerodin (5), and Scleroderris green (6) has been studied. It is shown that both C-1 and C-3 of 3 and 4 are derived from C-1 of acetate, and that C-2 of scleroderolide (4) is derived from C-2 of acetate while C-3 is derived from C-1 of acetate. As expected, C-1 and C-3 of Scleroderris green (6) originate from the carboxyl carbon of acetate, while C-2 originates from the methyl carbon of acetate. Complete 13C and 1H nuclear magnetic resonance spectra of these metabolites are reported. It has also been shown that ent-atrovenetin (ent-7a) is a metabolite of G. abietina.

1980 ◽  
Vol 58 (9) ◽  
pp. 928-931 ◽  
Author(s):  
Pierre L. Beaulieu ◽  
Veronique M. Morisset ◽  
Dennis G. Garratt

The observation of the magnetic nonequivalence of isopropyl methyl carbon resonances as a result of axial dissymmetry in 27 appropriately substituted allenes is reported. The magnitude of the nonequivalence Δ is more dependent upon the adjacent substituent group than upon the substituents which are bonded to the remote sp2 carbon of the allene. A mechanism based upon the transmission of substituent effects from the remote substituents to the collinear π orbitals is proposed.


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