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Presents complete assurance of the kinds of discounts passed through by way of many of the sessions of natural chemistry. Discusses mark downs in keeping with what bond or useful staff is diminished by means of assorted reagents. offers distinctive awareness to selective discounts which are compatible for the relief of 1 specific kind of bond or functionality with no affecting different bonds or capabilities found in an identical molecule.
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3. Cyclization of 6C-Substituted Hexopyranoses . . . . . . 4. Action of Acids on Hexoses and Their Derivatives . . . . . . . . . . 5. Thermal Degradation of Polysaccharides, Oligosaccharides, and ..................... Hexoses . . . . . . . . . 6. Miscellaneous Methods . . . . . . . 7. Total Synthesis from Acrolein ....................................... 111. General Properties of 1,6-Anhydrohexopyranoses ........................ IV. Reactions of 1,6-Anhydrohexopyranoses.
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Worth, Phytochemisiry, 6 , 4 2 3 4 3 1 (1967). “Professor T. S. Moore-Obituary,” E. J. Bourne, Nature, 214, 1063 (1967). “Ring Scission of Cyclic Acetals. Part 111, Reaction of Acetyl Trifluoroacetate with 1,3:2,5 :4,6Tri-O-methylene-~-mannitol,” T. G. Bonner, E. J. Bourne, and D. Lewis, J . Chem. , C , 2321-2336 (1967). “The Formation, under Kinetic Control, of a New Monoacetal (2,3-O-Butylidene-~Glucitol) from D-Glucitol and n-Butyraldehyde,” T. G. Bonner, E. J. Bourne, P. J. V. Cleare, and D.