Chemistry

Acid Derivatives: Volume 2 (1979)

Content:
Chapter 12 Radiation chemistry of acids, esters, anhydrides, lactones and lactams (pages 755–780): O. I. Micic and O. S. Gal
Chapter thirteen The electrochemistry of carboxylic acids and derivatives: Cathodic savings (pages 781–824): James P. Coleman
Chapter 14 Decarbonylation reactions of acid halides and aldehydes through chlorotris?(triphenylphosphine)rhodium(i) (pages 825–857): M. C. Baird
Chapter 15 Pyrolysis of acids and their derivatives (pages 859–914): R. Taylor
Chapter sixteen Transcarboxylation reactions of salts of fragrant carboxylic acids (pages 915–944): Josef Ratusky
Chapter 17 Micellar results upon deacylation (pages 945–1020): C. A. Bunton and L. S. Romsted
Chapter 18 The chemistry of thio acid derivatives (pages 1021–1062): J. Voss
Chapter 19 The synthesis of lactones and lactams (pages 1063–1330): James F. Wolfe and Michael A. Ogliaruso

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Phys. , 77, 620 (1973). 74. J. Lilie and R. Fessenden, J. Phys. O i e m . , 77,674 (1973). 75. R. S. Alger, T. H. Anderson and L. A. Webb, J. a i e m . , 30,695 (1959). 76. Y. Nakajima, S. Sat0 and S . Shids, Bull. , Japan, 42,2132 (1969). 77. P. B. Ayscough and J. P. Oversby, J. Oiem. , Faraday I, 7,1153 (1972). 78. Y. Noro, M. Ochiai, T. Miyazaki, A. Torikai, K. Fueki and Z. Kuri, J. Phys. 74, 63 (1970). 79. K. J. Mills and J. M. Nosworthy Peto, J. Chem. ,Faraday I,72, 1626 (1972). 80. A. S. Newton and P.

Newton, J. , 26,1764 (1957). 17. 4. Wu and D. R. , 57, 390 (1974). 18. A. R. ,47, 35 (1971). 19. A. R. , 50,41 (1972). 20. A. R. , 48,447 (1971). 21. -S. Wu and D. R. , 61, 374 (1975). 22. J. G. Burr, J. Phys. Chem, 61,1481 (1957). 23. G. E. Adams, J. H. Baxendale and R. D. Segwick. J. Phys. , 63,854 (1959). 24. R. H. Johnsen,J. Phys. , 63,2041 (1959). 25. Lj. Josimovic, J. Tepl? and 0. I. Mikid, J. Chem. 285 (1976). 26. B. Ayscough, K. P. K. Roy, Trans. Farad. ,67, 360 (1971). 27. S. LukaE, J.

They have claimed that a small electrochemical unit with a capacity of 10-1 5 tonslyear would produce salicylaldehyde at 40% of the cost of the chemically produced material. 99 million pounds3 (about 1800 tons), so that both of these units are a long way from commercial production size. Significant changes would have t o be made t o make either process truly commercial. The preparative results o n salicylic acid reduction are summarized in Table 2. The preparative features of this reaction are, thus, well established and more recently attention has been turned t o mechanistic questions.

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