Get Acid Derivatives: Volume 2 (1992) PDF

ISBN-10: 0470772506

ISBN-13: 9780470772508

ISBN-10: 047193111X

ISBN-13: 9780471931119

Best multinational researchers of their revered fields offer overall assurance of the entire theoretical, actual, artificial and analytical elements of acid derivatives in addition to their mechanistic and organic homes.

Content:
Chapter 1 basic and theoretical (pages 1–50): Harold Basch and Tova Hoz
Chapter 2 Thermochemistry of carboxylic acids and derivatives (pages 51–94): G. Pilcher
Chapter three Chiroptical houses of acid derivatives (pages 95–131): Jan Sandstrom
Chapter four Mass spectrometry of carboxylic acid derivatives (pages 133–151): Helge Egsgaard and Lars Carlsen
Chapter five Nuclear magnetic resonance of acids and acid derivatives (pages 153–226): Poul Erik Hansen
Chapter 6 ESR reports of natural loose radicals from carboxylic acids and their derivatives (pages 227–266): Michael J. Davies, Bruce C. Gilbert and Adrian C. Whitwood
Chapter 7 Vibrational research of acid derivatives (pages 271–303): Herman O. Desseyn
Chapter eight Acid–base houses of carboxylic acids, esters and amides (pages 305–369): Romuald I Zalewski
Chapter nine Syntheses and makes use of of isotopically labelled acid derivatives (pages 371–546): Mieczyslaw Zielinski and Marianna Kanska
Chapter 10 The chemistry of lactones and lactams (pages 547–614): G. V. Boyd
Chapter eleven the artificial makes use of of carboxylic acids and their derivatives (pages 615–701): Jeffrey Hoyle
Chapter 12 Vapour and gas?phase reactions of carboxylic acids and their derivatives (pages 703–746): Kenneth A. Holbrook
Chapter thirteen Mechanistic points. contemporary advancements bearing on mechanisms of acylation through carboxylic acid derivatives (pages 747–802): D. P. N. Satchell and R. S. Satchell
Chapter 14 Thio derivatives (pages 803–847): S. Kato and T. Murai
Chapter 15 Hydroxamic acids (pages 849–873): James W. Munson
Chapter sixteen The chemistry of amidoximes (pages 875–966): Demetrios N. Nicolaides and Evangelia A. Varella
Chapter 17 education and chemistry of ortho acids, ortho esters and ortho amides (pages 967–1030): Ulf Pindur
Chapter 18 fresh advancements relating carboxyl teams in biochemistry (pages 1031–1061): Alan H. Mehler
Chapter 19 Pharmacology of acid derivatives (pages 1063–1105): Abraham Danon and Zvi Ben?Zvi
Chapter 20 Photochemistry of esters, lactones and their thio analogues (pages 1107–1198): Hiroshi Suginome
Chapter 21 Radiation chemistry of fatty and amino acids (pages 1199–1248): S. V. Jovanovic and Lj. R. Josimovic
Chapter 22 Electrochemistry of carboxylic acids: mechanistic facets of Kolbe?type reactions (pages 1249–1270): Elisabet Ahlberg
Chapter 23 Rearrangements (pages 1271–1394): Miguel A. Miranda and Hermenegildo Garcia
Chapter 24 the applying of lipases in natural synthesis (pages 1395–1473): Gudmundur G. Haraldsson
Chapter 25 Diazoacetic acids and derivatives (pages 1475–1637): Oleg M. Nefedov, Evgenii A. Shapiro and Alexey B. Dyatkin
Chapter 26 Anion radicals of fragrant carboxylic acids and their derivatives: constitution and reactivity (pages 1639–1682): Isaak I. Bilkis

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Additional resources for Acid Derivatives: Volume 2 (1992)

Sample text

24. W. J. Stevens, H. Basch and M. Krauss, J. Chem. , 81, 6026 (1984). 25. W. Schneider and W. Thiel, J. Chem. , 86, 923 (1987). 26. H. Basch, W. J. Stevens and M. Krauss, Chem. Phys. , 109, 212 (1984). 27. H. Basch, Chem. Phys. , 136, 289 (1987); 2. Fu, G . W. Lemire, Y. M. Hamrick, S. Taylor, J. C. Shui and M. D. Morse, J. Chem. , 88, 3524 (1988). 28. S. F.

J. Defrees, D. J. Fox, R. A. Whiteside, R. Seeger, C. F. Melius, J. Baker, R. Martin, L. R. Kahn, J. J. P. Stewart, E. M. Fluder, S. Topiol and J. A. , Pittsburgh, PA, 1988. 5. H. Basch, in The Chemistry of Sulphinic Acids, Esters and Their Derivatives, (Ed. S . Patai), Chap. 2, Wiley, Chichester, 1990, p. 9. 6. H. Basch and T. Hoz, in The Chemistry of Sulphonic Acids, Esters and Their Derivatives, (Eds. S . Patai and Z. Rappoport), Chap. 1, Wiley, Chichester, 1991, p. 1. 7. M. B. Robin, F. A. Bovey and H.

FIGURE 24. Metal ion-glycine (I-C),metal = Pt (top number) and Au. Bond lengths in angles in degrees A, bond (9--- FIGURE 25. Metal ion-glycine (11-D),metal = Ni (top number) and Cu. Bond lengths in A, bond angles in degrees 1. General and theoretical FIGURE 26. Metal ion-glycine (11-D),metal = Pt (top number) and Au. Bond lengths in angles in degrees 31 A, bond I r'lGURE 27. 0-Protonated glycine I with inverted amine group. Same as 0-protonated glycine A, bond angles in degrees 11. Bond lengths in 38 Harold Basch and Tova Hoz structures, it must be that local, and not overall molecular, dipole-moment forces dominate the interactions and determine the complex adduct geometries.

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Acid Derivatives: Volume 2 (1992)


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