Download Ciba Foundation Symposium - Chemistry and Biology of by MARGARET WOLSTENHOLME' 'G E W ; CAMERON PDF
By MARGARET WOLSTENHOLME' 'G E W ; CAMERON
Chapter 1 Chairman's starting feedback (page 1): A. Albert
Chapter 2 Ring?Opening Reactions of Pteridines (pages 2–34): E. C. Taylor
Chapter three The Alkylation of Pteridines (pages 35–48): H. C. S. Wood
Chapter four The relief and Reoxidation of a few 8?Substituted Pteridines (pages 49–61): Gertrude B. Elion
Chapter five The Monosubstituted Pteridines (pages 62–73): D. J. Brown
Chapter 6 a few features of the Ultraviolet Absorption Spectra of the Pteridines (pages 74–92): S. F. Mason
Chapter 7 using o?Aminonitroso Compounds within the Synthesis of Pteridines and a few Analogous Ring structures (pages 93–103): G. M. Timmis, D. G. I. Felton and T. S. Osdene
Chapter eight fresh advancements in Pteridine Synthesis (pages 104–123): John A. Carbon, Robert B. Garland, Dale R. Hoff, Charles F. Howell, William R. Sherman and E. C. Taylor
Chapter nine Chromatographic and Electrophoretic reviews of Pteridines (pages 124–134): M. Polonovski, H. Jerome and P. Gonnard
Chapter 10 The structure of Urothione (pages 135–142): R. Tschesche
Chapter eleven The Pteridines of Drosophila Melanogaster (pages 143–158): Hugh S. Forrest and Herschel ok. Mitchell
Chapter 12 The structure of Fluorescyanine (pages 159–164): F. Korte
Chapter thirteen New Observations on Fluorescyanine B (pages 165–172): M. Polonovski, R.?G. Busnel, H. Jerome and M. Martinet
Chapter 14 Sulphonamide Derivatives of Pteridines (pages 173–182): Marvin J. Fahrenbach, Kenneth Collins, Martin E. Hultquist, James M. Smith and Donna B. Cosulich
Chapter 15 a few Dipyrimidopyrazines (Pyrimidopteridines) (pages 183–192): Elvira A. Falco and George H. Hitchings
Chapter sixteen Structural stories on Pyrimidopteridines. The constitution of “Bis?Alloxazine” and “Diuracilpyridazine” (pages 193–203): E. C. Taylor, Cornelius ok. Cain and Harvey M. Loux
Chapter 17 a few Unresolved difficulties (pages 204–219): Adrien Albert
Chapter 18 Metabolic kinfolk among P?Aminobenzoic Acid and Folic Acid in Micro?Organisms (pages 220–236): D. D. Woods
Chapter 19 The functionality of Folic Acid within the Biosynthesis of Purine and Pyrimidine Derivatives (pages 237–252): R. H. Nimmo?Smith
Chapter 20 the results of Folic Acid Analogues at the progress and mobilephone department of Micro?Organisms (pages 253–271): M. Webb
Chapter 21 Antimetabolic and Antimicrobial houses of yes 2:4?Diaminopteridines (pages 272–289): H. O. J. Collier
Chapter 22 Derivatives of Condensed Pyrimidine structures as Antimetabolites (pages 290–303): George H. Hitchings, Gertrude B. Elion and Samuel Singer
Chapter 23 The organic task of Folic Acid and likely Substituted Pteridines for Tetrahymena (pages 304–313): George W. Kidder
Chapter 24 The Yellow Pigment of the Argentaffine Cells of the Mammalian Gastro?Intestinal Tract (pages 314–328): W. Jacobson
Chapter 25 The Mode of motion of Folic Acid Antagonists and the functionality of the Leuconostoc Citrovorum issue (pages 329–355): W. Jacobson
Chapter 26 the results of Folic Acid Antagonists on Embryonic improvement (pages 356–365): Ruth Bellairs
Chapter 27 experiences on Pteridine Metabolism (pages 366–384): Dorris J. Hutchison and Joseph H. Burchenal
Chapter 28 a few features of Disordered Folic Acid Metabolism in guy (pages 385–406): Ronald H. Girdwood
Chapter 29 prevalence of Hepatic Fibrosis in youngsters with Acute Leuk?mia taken care of with Folic Acid Antagonists (pages 407–413): Jacob Colsky
Chapter 30 Chairman's final feedback (pages 414–416): W. Jacobson
Read or Download Ciba Foundation Symposium - Chemistry and Biology of Pteridines PDF
Similar chemistry books
The booklet is dedicated to the honor of different techniques occurring in skinny motion pictures and at surfaces. because the most crucial physico-chemical phenomena in such media are followed through the rearrangement of an intra- and intermolecular coordinates and for this reason a surrounding molecular ensemble, the idea of radiationless multi-vibrational transitions is used for its description.
Within the final region century there were purely seminal contributions within the box of natural stereochemistry - either by way of Kurt Mislow and his coworkers - ones that experience clarified the elemental thoughts of stereotopicity and chirotopicity. no longer withstanding a couple of different sporadic contributions by means of others, to this point there were no systematic makes an attempt to unify and improve the conceptual framework and terminology of natural stereochemistry.
The Alkaloids: Chemistry and body structure V19. content material: conceal; The Alkaloids: Chemistry and body structure, quantity XIX; Copyright web page; Contents; checklist of members; Preface; Contents of prior quantity; bankruptcy 1. Sceletium Alkaloids; I. old heritage; II. the hoop structures of Sceletium Alkaloids; III.
- Taschenatlas der Umweltchemie
- Handbook on the Physics and Chemistry of Rare Earths, Volume 37: Optical Spectroscopy (Handbook on the Physics and Chemistry of Rare Earths)
- Advanced Practical Medicinal Chemistry
- Advanced Dairy Chemistry: Volume 1A: Proteins: Basic Aspects (4th Edition)
Extra resources for Ciba Foundation Symposium - Chemistry and Biology of Pteridines
J . Amer. chem. , 75, 1904. , and ERICKSON, A. E. (1945). J. Amer. chem. , 67, 802. , and BULOW,M. (1933). , and PURRMANN, R. (1939). , 539, 179. , and PURRMANN, R. (1940). , 544, 163. , and TARTTER, A. (1940). , 543,287. WITTLE,E. ,VANDENBELT, J. , and PFIFFNER, J. J. ) J . Amer. chem. , 69, 1786. Woon, H. C. S. Personal communication. [Discussion of Dr. Taylor's paper was postponed until after that of Dr. E. W. W. &Margaret P. P. Cameron G. Margaret Cameron Copyright 01954 Ciba Foundation Symposium Copyright © 1954 Ciba Foundation THE ALKYLATION OF PTERIDINES H .
REFERENCES ALBERT, A. Personal communication. ALBERT,A. (1952). Quart. Rev. chem. , 6, 197. , and BROWN, D. J. (1953). J . chem. , 74. , BROWN, D. , and CHEESEMAN, G. (1951). J. chem. , 474. 5. , BROWN, D. , and CHEESEMAN,G. J. chem. , 1620. 6. , BROWN, D. , and CHEESEMAN,G. (19526). J. chem. , 4219. E. , Jr. (1948). 7. CAIN,C . , MALLETTE, M. , and TAYLOR, J . Amer. chem. , 70, 3026. 8. KING,F. , and SPENSLEY, P. C. (1952). J. chem. , 2144. N. , and CURTIN, D. Y. (1946). J . org. , 11, 341. 9.
A similar example has been reported in the purine group by Biltz and Sauer (1931). Methylation of Q-methylxanthine with methyl sulphate gave 8:9-dimethylxanthine. The methylation of 2-hydroxypteridine and of 6-hydroxypteridine has been investigated using similar methods. In neither case did any reaction take place. It is interesting to note that these two pteridine derivatives exist as very stable monohydrates. The failure to react with alkylating agents may, in some way, be connected with this water of crystallization.