Major 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 houses.
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 stories 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 homes 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 substitute 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 facets. contemporary advancements pertaining to mechanisms of acylation by way of 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 instruction and chemistry of ortho acids, ortho esters and ortho amides (pages 967–1030): Ulf Pindur
Chapter 18 contemporary advancements bearing on 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 features 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 info for Acid Derivatives: Volume 2 (1992)
070 for 11. However, local dipole-moment forces are expected to be dominant and these should be probed with metal ions. Such calculations are currently underway. The formate anion is shown in Figure 32 and the geometric structures of the Ni+and Pt+-formate complexes are given in Figure 33. Both formate and formamidate anion ligands and their metal complexes were calculated in the TZV + basis set. The corresponding syn formic acid and formamide were also re-optimized in this basis set for comparison purposes.
TZV + basis = Ni (top number) and Pt. Bond lengths in A, bond 42 Harold Basch and Tova Hoz FIGURE 34. Formamidate anion. Bond lengths in A. bond angles in degrees. 098 FIGURE 35. Metal ion-formamidate anion; metal = Ni (top number) and Pt. Bond lengths in bond angles in degrees. TZV + basis A. 1. General and theoretical 43 FIGURE 36. Metal ion--glycine zwitterion, metal-Ni (top number) and Cu. Bond lengths i n A, bond angles in degrees and influence (see later) of the amino acid and protein structures are probably the dominant factors here.
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. Basch, in The Chemistry of the Amides, (Ed. J. Zabicky), Chap. 1, Wiley, London, 1970, p. 1. 8. M. Krauss, H. Basch and K. J. Miller, J. Am. Chem. , 110, 4517 (1988); Chem.