The vinylogation of aldehydes: An improved method for the preparation of alpha formylethylidenetriphenylphosphorane, and an improved alpha silyl imine reagent of propionaldehyde
Schlessinger, R. H.; Poss, M. A.; Richardson, S.; Lin, P. The vinylogation of aldehydes: an improved method for the preparation of alpha formylethylidenetriphenylphosphorane, and an improved alpha silyl imine reagent of propionaldehyde. Tetrahedron Lett. 1985, 26, 2391-2394.
A highly selective method for the synthesis of (E)-α-methyl-α,β- unsaturated aldehydes
Desmond, R.; Mills, S. G.; Volante, R. P.; Shimkai, I. A highly selective method for the synthesis of (E)-α-methyl-α,β- unsaturated aldehydes. Tetrahedron Lett. 1988, 29, 3895-3898.
Facile biphasic deprotection of aldehyde dimethylhydrazones with aqueous hydrochloric acid
submitted for publication
Petroski, R. J. Facile biphasic deprotection of aldehyde dimethylhydrazones with aqueous hydrochloric acid. Lett. Org. Chem. 2007 (submitted for publication).
Hardie, J, Minks, A. K, Eds, CABI Publishing; New York
Bartelt, R. J. Sap beetles. In Pheromones of Non-Lepidopteran Insects Associated with Agricultural Plants; Hardie, J., Minks, A. K., Eds.; CABI Publishing; New York, 1999; pp 69-89.
Aggregation pheromone of Carpophilus lugubris new pest management tools for the nitidulid beetles
Naturally Occurring Pest Bioregulators; Hedin, P. A, Ed, American Chemical Society: Washington, DC
Bartelt, R. J.; Dowd, P. F.; Plattner, R. D. Aggregation pheromone of Carpophilus lugubris new pest management tools for the nitidulid beetles. In Naturally Occurring Pest Bioregulators; Hedin, P. A., Ed.; ACS Symposium Series 449; American Chemical Society: Washington, DC, 1991; pp 27-40.
Synthesis of nitidulid beetle pheromones: Alkyl-branched tetraene hydrocarbons
Bartelt, R. J.; Weisleder, D.; Plattner, R. D. Synthesis of nitidulid beetle pheromones: alkyl-branched tetraene hydrocarbons. J. Agric. Food Chem. 1990, 2192-2196.
Dramatic concentration dependence of stereochemistry in the Wittig reaction. Examination of the lithium salt effect
Reitz, A. B.; Norty, S. O.; Jordon, A. J.; Mutter, M. S.; Maryanoff, B. E. Dramatic concentration dependence of stereochemistry in the Wittig reaction. Examination of the lithium salt effect. J. Org. Chem. 1986, 51, 3302-3308.
13C-Predictive software, version 6.0, is available from Advanced Chemistry Development, Toronto, Ontario, Canada
13C-Predictive software, version 6.0, is available from Advanced Chemistry Development, Toronto, Ontario, Canada.
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Ford-Moore, A. H.; Perry, B. J. Diisopropyl methylphosphonate. Org. Synth. 31, 1951, 33-35.
Ford-Moore, A. H.; Perry, B. J. Diisopropyl methylphosphonate. Org. Synth. 31, 1951, 33-35.
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Diethyl ethylformyl-2-phosphonate can also be named (1-methyl-2-oxoethyl) phosphonic acid diethyl ester, and diethyl 1-propylformyl-2-phosphonate can also be named (1-formylpropyl)-phosphonic acid diethyl ester. Diethyl ethylformyl-2-phosphonate dimethylhydrazone 2 can also be named [2-(dimethylhydrazino)-1-methylethyl]phosphonic acid diethyl ester, and diethyl 1-propylformyl-2-phosphonate dimethylhydrazone 3 can also be named [1-(dimethylhydrazinomethyl)propyl]phosphonic acid diethyl ester.
Diethyl ethylformyl-2-phosphonate can also be named (1-methyl-2-oxoethyl) phosphonic acid diethyl ester, and diethyl 1-propylformyl-2-phosphonate can also be named (1-formylpropyl)-phosphonic acid diethyl ester. Diethyl ethylformyl-2-phosphonate dimethylhydrazone 2 can also be named [2-(dimethylhydrazino)-1-methylethyl]phosphonic acid diethyl ester, and diethyl 1-propylformyl-2-phosphonate dimethylhydrazone 3 can also be named [1-(dimethylhydrazinomethyl)propyl]phosphonic acid diethyl ester.
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Direct conversion of phosphates to alpha-lithio phosphonates with alkyllithiums
Teulade, M.-P.; Savignac, P. Direct conversion of phosphates to alpha-lithio phosphonates with alkyllithiums. Tetrahedron Lett. 1987, 28, 405-408.