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Edmundo Alfredo Ruveda

Edmundo Alfredo Ruveda, Argentine organic chemist (Corrientes 18 March 1934 – Rosario 14 December 2018)



With M.D. Preite, J, Zinczuk, M.I. Colombo, J.A. Bacigalupo & M. Gonzalez Sierra. Resolution and absolute configuration of a tricyclic lactone. A potentially useful precursor of highly functionalized terpenoids. Tetrahedron Asymmetry 4:17, 1993

With M. Gonzalez Sierra, A.C.Olivieri & M.I. Colombo. The absolute stereochemistry of the novel dioxiaspiroditerpenoids strictanonic and grindelistrictiacid . Stereoselective synthesis of strictanonic acid methyl esther and its C6 epimer. J. Chem. Soc. Perkin Trans. I 1:1393, 1989

With T.S. Kaufman & M. Gonzalez Sierra. Synthesis of an Alberta oil sand bitumen CJ10 tricyclic carboxylic acid bering a novel diterpenoid skeleton (1988)

With A.C. Olivieri & M. Gonzalez Sierra. Stereoselective synthesis of the novel bisnorditerpene grindelistrictic acid, isolated from Grindelia strictis. J.Org. Chem. 51:2824, 1986

With M.P. Mischne & M. Gonzalez Sierra. Synthesis of the novel marine diterpenes isocopal-12-en-15,16-dial, 14-epi-Isocopal-12-en-15,16 dial and 15-acetoxy-Isocopal-12-en-16-al from methyl isocopalate. J. Org. Chem. 49:2035, 1984

With M. Gonzalez Sierra & R.A. Spanevello. Simple and efficient synthesis of 3-oxo-2,6,6-trimethylcyclohex-1-ene-1-carboxylic acid, a key synthon for rac-strigol. J. Org. Chem. 48:5111, 1983

With D.S. de Miranda, G. Brendolan, P.M. Imamura, M. Gonzalez Sierra & A.J. Marsaioli. Stereoselective synthesis of the enantiomer of the novel marine diterpene isoagatholactone, it-13,16: sporgiadien-12-aol, and the parent hydocarbon isocopalane from methyl isocopalate. J. Org. Chem. 46(24), 1981

With P.M. Imamura & M. Gonzalez Sierra. Stereoselective synthesis of the novel marine diterpene (+) isoagatholactone. Chem. Soc. Chem. Comm. 734 (1981)

With H.A. Priestap & J.D. Bonafede. Argentilactone, a novel 5-hydroxyacid lactone from Aristolochia argentina. Phytochem. 16(10):1579-82, 1977