Issue 0, 1979

Structural investigation of lac resin. Part 14. Model esters related to lac resin

Abstract

Model esters formed from the 12- and 15-carboxy-functions of shellolic acid and its 2-epimer with the C-16-position of methyl threo-aleuritate are reported. While stearate esters involving the hydroxy-groups of the above two terpenes were readily obtained through the acid chloride or the mixed anhydride procedure, the corresponding mixed threo-aleuritic–carbonic anhydride failed to react. The results indicated the greater stability and preferential ester formation with mixed stearic–carbonic anhydride at C-13 rather than at C-10.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 2167-2170

Structural investigation of lac resin. Part 14. Model esters related to lac resin

G. B. V. Subramanian, U. Mejumdar, R. Nuzhat, V. K. Mahajan and K. N. Ganesh, J. Chem. Soc., Perkin Trans. 1, 1979, 2167 DOI: 10.1039/P19790002167

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