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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Sunspots-Congresses. ; Electronic books.
    Description / Table of Contents: Proceedings of the NATO Advanced Research Workshop on The Theory of Sunspots, Cambridge, U.K., September 22-27, 1991.
    Type of Medium: Online Resource
    Pages: 1 online resource (422 pages)
    Edition: 1st ed.
    ISBN: 9789401127691
    Series Statement: Nato Science Series C: Series ; v.375
    Language: English
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  • 2
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Pyrimidines. ; Heterocyclic compounds. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (338 pages)
    Edition: 1st ed.
    ISBN: 9780470188385
    Series Statement: Chemistry of Heterocyclic Compounds: a Series of Monographs ; v.80
    Language: English
    Note: Intro -- FUSED PYRIMIDINES: Miscellaneous Fused Pyrimidines -- Contents -- CHAPTER I. PYRIDOPYRIMIDINES -- 1. Introduction -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrido[3,2-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyridines -- B. Synthesis of Pyrido[4,3-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyridines -- C. Synthesis of Pyrido[3,4-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyridines -- D. Synthesis of Pyrido[2,3-d]pyrimidines -- (1) From Pyrimidines -- (a) Formation of Bond 4a-5 -- (b) Formation of Bond 5-6 -- (c) Formation of Bond 7-8 -- (d) Formation of Bond 8-8a -- (2) From Pyridines -- (a) Formation of Bond 8a-l -- (b) Formation of Bond 1-2 -- (c) Formation of Bond 2-3 -- (d) Formation of Bond 3-4 -- (e) Formation of Bond 4-4a -- 3. Reactions -- A. Of Pyrido[3,2-d]pyrimidines -- B. Of Pyrido[4,3-d]pyrimidines -- C. Of Pyrido[3,4-d]pyrimidines -- D. Of Pyrido[2,3-d]pyrimidines -- (1) With Nucleophiles -- (2) With Electrophiles -- (3) Reductions -- (4) Oxidations -- 4. Patent Literature -- 5. Tables -- Table 1. Derivatives of Pyrido[3,2-d]pyrimidine -- Table 2. Derivatives of Pyrido[4,3-d]pyrimidines -- Table 3. Derivatives of Pyrido[3,4-d]pyrimidines -- Table 4. Derivatives of 2,4-Diaminopyrido[2,3-d]pyrimidines -- Table 5. Derivatives of 2-Amino-4-hydroxypyrido[2,3-d]pyrimidines -- Table 6. Derivatives of 2-Aminopyrido[2,3-d]pyrimidines -- Table 7. Derivatives of 4-Aminopyrido[2,3-d]pyrimidines -- Table 8. Derivatives of 2,4-Dihydroxypyrido[2,3-d]pyrimidines -- Table 9. Derivatives of 2-Hydroxypyrido[2,3-d]pyrimidines -- Table 10. Derivatives of 4-Hydroxypyrido[2,3-d]pyrimidines -- Table 11. Derivatives of 4-Amino-2-mercaptopyrido[2,3-d]pyrimidines -- Table 12. Derivatives of 4-Hydroxy-2-mercaptopyrido[2,3-d]pyrimidines. , Table 13. Derivatives of 2-Mercapto- and 4-Mercaptopyrido[2,3-d]pyrimidines -- Table 14. Derivatives of Pyrido[2,3-d]pyrimidines -- 6. References -- CHAPTER II. PYRANO- AND THIOPYRANOPYRIMIDINES -- 1. Nomenclature -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrano[2,3-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyrans -- (3) From Nonheteroaromatic Precursors -- B. Synthesis of Pyrano[4,3-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyrans -- C. Synthesis of Pyrano[3,2-d]pyrimidines -- (1) From Pyrimidines -- (2) From Pyrans -- D. Synthesis of Thiopyrano[2,3-d]pyrimidines -- (1) From Pyrimidines -- (2) From Thiopyrans -- E. Synthesis of Thiopyrano[3,4-d]pyrimidines -- F. Synthesis of Thiopyrano[4,3-d]pyrimidines -- 3. Reactions -- A. With Nucleophilic Reagents -- B. Other Reactions -- 4. Patent Literature -- 5. Tables -- Table 1. The Pyrano[2,3-d]pyrimidines -- Table 2. The Pyrano[4,3-d]pyrimidines -- Table 3. Miscellaneous Pyranopyrimidines -- Table 4. The Thiopyrano[2,3-d]pyrimidines -- Table 5. The Thiopyrano[3,4-d]pyrimidines -- 6. References -- CHAPTER III. PYRIMIDOPYRIMIDINES -- 1. Nomenclature -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrimido[4,5-d]pyrimidines -- (1) From Pyrimidines with Amino Groups Adjacent to Hydrogen -- (2) From Pyrimidines with Amino Groups Adjacent to Nitriles -- (3) From Pyrimidines with Amino Groups Adjacent to Amides -- (4) From Pyrimidines with Amino Groups Adjacent to Esters -- (5) From Pyrimidines with Amino Groups Adjacent to Aldehyde or Ketone Groups (or Their Derivatives) -- (6) From Pyrimidines with Amino Groups Adjacent to Substituted Methyl Groups -- (7) From Pyrimidines with Miscellaneous Groups Adjacent to Each Other -- (8) From Pyrimidines Fused to Other Rings -- (9) From Nonheteroaromatic Precursors -- B. Synthesis of Pyrimido[5,4-d]pyrimidines. , (1) From Pyrimidines with Amino Groups Adjacent to Carboxylic Acids -- (2) From Pyrimidines with Amino Groups Adjacent to Carboxylic Acid Derivatives -- (3) From Pyrimidines with Miscellaneous Groups Adjacent to Each Other -- (4) By Rearrangement of Other Heterocyclic Systems -- (5) From Nonheteroaromatic Precursors -- 3. Reactions -- A. Of Pyrimido[4,5-d]pyrimidines with Nucleophiles -- B. Other Reactions of Pyrimido[4,5-d]pyrimidines -- C. Of Pyrimido[5,4-d]pyrimidines with Nucleophiles -- D. Other Reactions of Pyrimido[5,4-d]pyrimidines -- 4. Patent Literature -- 5. Tables -- Table 1. The Pyrimido[4,5-d]pyrimidines That Have No Oxo or Thioxo Groups -- Table 2. The Pyrimido[4,5-d]pyrimidines with One Oxo or Thioxo Group -- Table 3. The Pyrimido[4,5-d]pyrimidines with Two Oxo and/or Thioxo Groups -- Table 4. The Pyrimido[4,5-d]pyrimidines waith Three or Four Oxo and/or Thioxo Groups -- Table 5. Miscellaneous Pyrimido[4,5-d]pyrimidines -- Table 6. The Pyrimido[5,4-d]pyrimidines with No Oxo, Thioxo, or Halogen Groups -- Table 7. The Pyrimido[5,4-d]pyrimidines with No Oxo or Thioxo Groups But with Halogen Groups -- Table 8. The Pyrimido[5,4-d]pyrimidines with Oxo and/or Thioxo Groups -- Table 9. Miscellaneous Pyrimido[5,4-d]pyrimidines -- 6. References -- CHAPTER IV. PYRIMIDOPYRIDAZINES -- 1. Nomenclature -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrimido[4,5-c]pyridazines -- (1) From Pyrimidines -- (2) From Pyridazines -- B. Synthesis of Pyrimido[4,5-d]pyridazines -- (1) From Pyrimidines -- (2) From Pyridazines -- C. Synthesis of Pyrimido[5,4-c]pyridazines -- (1) From Pyrimidines -- (2) From Pyridazines -- 3. Reactions -- A. Of Pyrimido[4,5-c]pyridazines -- B. Of Pyrimido[4,5-d]pyridazines -- C. Of Pyrimido[5,4-c]pyridazines -- 4. Patent Literature -- 5. Tables -- Table 1. The Pyrimido[4,5-c]pyridazines. , Table 2. The Pyrimido[4,5-d]pyridazines -- Table 3. The Pyrimido[5,4-c]pyridazines -- Table 4. Miscellaneous Pyrimidopyridazines -- 6. References -- CHAPTER V. PYRIMIDOOXAZINES AND PYRIMIDOTHIAZINES -- 1. Nomenclature -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrimido[4,5-b][l,4]oxazines -- (1) From Pyrimidines -- B. Synthesis of Pyrimido[5,4-b][l,4]oxazines -- (1) From Pyrimidines -- C. Synthesis of Pyrimido[4,5-e] [l,3]oxazines -- (1) From Pyrimidines -- D. Synthesis of Pyrimido[4,5-d][l,3]oxazines -- (1) From Pyrimidines -- (2) From Other Rings -- E. Synthesis of Pyrimido[5,4-d][l,3]oxazines -- (1) From Pyrimidines -- F. Synthesis of Pyrimido[4,5-d][1,4]thiazines -- (1) From Pyrimidines -- (2) From Other Rings -- G. Synthesis of Pyrimido[5,4-b][l,4]thiazines -- (1) From Pyrimidines -- (2) From Thiazines -- H. Synthesis of Pyrimido[4,5-d][l,4]thiazines -- (1) From Pyrimidines -- I. Synthesis of Pyrimido[5,4-e] [l,3]thiazines -- (1) From Pyrimidines -- 3. Reactions -- A. With Nucleophilic Reagents -- B. Ring-Opening Reactions -- C. Other Reactions -- 4. Patent Literature -- 5. Tables -- Table 1. The Pyrimido[4,5-b] [ 1,4]oxazines -- Table 2. The Pyrimido[5,4-b] [l,4]oxazines -- Table 3. The 2//-Pyrimido[4,5-e][l,3]oxazines -- Table 4. The Pyrimido[4,5-d][l,3]oxazines -- Table 5. The 4W-Pyrimido[5,4-d][l,3]oxazines -- Table 6. Miscellaneous Pyrimidooxazines -- Table 7. The Pyrimido[4,5-b][1,4]thiazines -- Table 8. The Pyrimido[5,4-b][l,4]thiazines -- Table 9. Miscellaneous Pyrimidothiazines -- 6. References -- CHAPTER VI. PYRIMIDOTRIAZINES -- 1. Nomenclature -- 2. Methods of Synthesis of the Ring System -- A. Synthesis of Pyrimido[5,4-e]-l,2,4-triazines -- (1) From Pyrimidines with Adjacent Amino and Hydrazino Groups -- (2) From Pyrimidines with Adjacent Amino and Chloro Groups. , (3) From Pyrimidines with 5-Nitroso or 5-Nitro Groups -- (4) From Pyrimidines with Adjacent Hydrazino Groups -- (5) From Pyrimidines with a 6-Azido Group -- (6) From Pyrimidines with Adjacent Amino Groups -- (7) From Triazines -- (8) From Other Heterocyclic Rings -- B. Synthesis of Pyrimido[4,5-e]-l,2,4-triazines -- (1) From Pyrimidines -- (2) From Triazines -- (3) From Purines -- C. Synthesis of Pyrimido[5,4-d]-l,2,3-triazines -- D. Synthesis of Pyrimido[4,5-d]-l,2,3-triazines -- 3. Reactions -- A. Of Pyrimido[5,4-e]-l,2,4-triazines -- (1) Simple Group Transformations -- (a) Oxidation Reactions -- (b) Functional Group Interconversions -- (c) Covalent Addition -- (2) Ring-Opening Reactions -- (a) With Retention of One of The Heteroaromatic Rings -- (b) With Formation of New Heteroaromatic Rings -- B. Of Pyrimido[4,5-e]-1,2,4-triazines -- (1) Simple Group Transformations -- (2) Ring-Opening Reactions -- C. Of Pyrimido[5,4-d]-1,2,3-triazines -- 4. Patent Literature -- 5. Tables -- Table 1. The Pyrimido[5,4-e]-1,2,4-triazines That Have No Oxo or Thioxo Groups -- Table 2. The Pyrimido[5,4-e]-1,2,4-triazines with One Oxo or Thioxo Group -- Table 3. The Pyrimido[5,4-e]-1,2,4-triazines with Two Oxo or Thioxo Groups -- Table 4. The Pyrimido[5,4-e]-1,2,4-triazines with Three Oxo Groups -- Table 5. Miscellaneous Pyrimido[5,4-e]-1,2,4-triazines -- Table 6. The Pyrimido[4,5-e]-1,2,4-triazines with No Oxo or Thioxo Groups -- Table 7. The Pyrimido[4,5-e]-1,2,4-triazines with One Oxo Group -- Table 8. The Pyrimido[4,5-e]-1,2,4-triazines with Two Oxo or Thioxo Groups -- Table 9. The Pyrimido[4,5-e]-1,2,4-triazines with Three Oxo or Thioxo Groups -- Table 10. Miscellaneous Pyrimido[4,5-e]-1,2,4-triazines -- Table 11. The Pyrimido[5,4-d]-1,2,3-triazines -- Table 12. Miscellaneous Pyrimido[5,4-d]-1,2,3-triazines -- 6. References -- INDEX.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Skeletal radiology 21 (1992), S. 407-409 
    ISSN: 1432-2161
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 57 (1992), S. 433-434 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 7
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 1961-1967 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 2328-2334 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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