By John H.; Wiley; Lister, John Henry; John Wiley & Sons Wiley-Interscience Lister
Creation to the Purines (H1).
Synthesis from Pyrimidines.
Purines Syntheses from Imidazoles and different Precursors (H 91).
Purine and C -Alkyl, C -Aryl and N -Alkyl Derivatives (H 117).
Halogenopurines (H 135).
Oxo-(Hydroxy-) and Alkoxypurines (H 203).
Thioxo- and Selenoxopurines and Derivatives (H 269).
The Amino (and Amino-Oxo) Purines (H 309).
The Purine Carboxylic Acids and comparable Derivatives (H 367).
Nitro-, Nitroso-, and Arylazopurines (H 401).
Purine-N -Oxides (H 409).
The decreased Purines (H 427).
Enlarged Purine-Containing buildings (New).
The Spectra of Purines (H 507).
Systematic Tables of straightforward Purines.
Chapter I advent to the Purines (H1) (pages 1–20):
Chapter II Synthesis from Pyrimidines (pages 21–60):
Chapter III Purines Syntheses from Imidazoles and different Precursors (H91) (pages 61–82):
Chapter IV Purine and C?Alkyl, C?Aryl, and N?Alkyl Derivatives (H117) (pages 83–98):
Chapter V Halogenopurines (H135) (pages 99–132):
Chapter VI Oxo?(Hydroxy?) and Alkoxypurines (H203) (pages 133–178):
Chapter VII Thioxo? and Selenoxopurines and Derivatives (H269) (pages 179–212):
Chapter VIII The Amino (and Amino?Oxo)Purines (H309) (pages 213–282):
Chapter IX The Purine Carboxylic Acids and comparable Derivatives (H367) (pages 283–302):
Chapter X Nitro?, Nitroso?, and Arylazopurines (H401) (pages 303–306):
Chapter XI Purine?N?Oxides (H409) (pages 307–324):
Chapter XII The diminished Purines (H427) (pages 325–336):
Chapter XIII Enlarged Purine?Containing buildings (New) (pages 337–346):
Chapter XIV The Spectra of Purines (H507) (pages 347–384):
Chapter XV Systematic Tables of easy Purines (pages 385–424):
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Extra info for Chemistry of Heterocyclic Compounds: The Purines, Supplement 1, Volume 54
Y. Cyclizationwith Miscellaneous Reagents (New) This section embraces cyclizing reagents reported in the literature which cannot be accommodated comfortably into any of the orthodox categories. All are bifunctional and give rise to 8-substituted purines. Ethyl benzimidate, as Using 4,5-Diaminopyrimidines(The Traube Synthesis) 43 0 EtO-C-Ph 'N I H CH2Ph 97 96 98 100 (R' = p-Tolucoesulfonyl) 99 hydrochloride salt (W), in hot ethanol with 4,5-diamino-3-benzyl-3,6-dihydro-6oxopyrimidine (reflux, 3 h) forms 3-benzyl-8-phenylhypo~anthine~~~ (97).
Cyclization with Dithioformic Acid (H38) . . . . . . . . . . . . Cyclization with Other Carboxylic Acids (H41) . . . . . . . . . . . Cyclization with Acid Anhydrides (H44) . . . . . . . . . . . . Cyclization with Acid Chlorides (H47) . . . . . . . . . . . . . Cyclization with Orthoesters and Diethoxymethyl Acetate (H50) . . . . . H . Cyclization with Formamide (H53) . . . . . . . . . . . . . . I . Cyclization with Other Amides (H56) .
U . Cyclization with Chlorocarbonic Ester (H68) . . . . . . . . . . . V . Cyclizaiion with Aldehydes and Ketones (H69) . . . . . . . . . . W . Cyclization with Cyanogen Derivatives ( M I ) . . . . . . . . . . . X . Cyclimtion with Teiraalkoxymethanes and Thioxo Analogs . . . . . . . Y . Cyclization with Miscellaneous Reagents (New) . . . . . . . . . . Syntheses from 4-Amino-5-nitro- and 4-Amino-5-nitroso-pyrimidines (H72) and from 4-Amino-5-azopyrimidines (New) .