Chemistry

Chemistry of Heterocyclic Compounds: The Purines, Supplement by John H.; Wiley; Lister, John Henry; John Wiley & Sons

By John H.; Wiley; Lister, John Henry; John Wiley & Sons Wiley-Interscience Lister

Advent 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 similar Derivatives (H 367).

Nitro-, Nitroso-, and Arylazopurines (H 401).

Purine-N -Oxides (H 409).

The lowered Purines (H 427).

Enlarged Purine-Containing buildings (New).

The Spectra of Purines (H 507).

Systematic Tables of straightforward Purines.

References.

Index.Content:
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 similar 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 straightforward Purines (pages 385–424):

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Additional info for Chemistry of Heterocyclic Compounds: The Purines, Supplement 1, Volume 54

Example text

N . Cyclization with Thiourea (H60) . . . . . . . . . . . . . . 0. Cyclization with Cyanates. lsocyanates and Derivatives (H61) . . . . . . P. Cyclization with lsothiocyanates (H62) . . . . . . . . . . . . . R . Cyclization with Carbon Disulfide (H64) . . . . . . . . . . . . S. Cyclization with Phosgene(H67) . . . . . . . . . . . . . . U . Cyclization with Chlorocarbonic Ester (H68) . . . . . . . .

M. From Pyrimido [4,5-d][ 1, 4ldiazepines (New) . . . . . . . . . . . 21 22 24 24 26 29 3U 32 32 33 34 34 35 35 36 37 37 37 38 41 41 42 44 44 47 48 51 51 54 54 54 55 55 56 56 57 58 59 59 Synthesis from Pyrimidines 22 1. USING 4,5-DIAMINOPYRIMIDINES (THE TRAUBE SYNTHESIS) B. Cyclization with Formic Acid (H33) Although now largely superseded by trialkyl orthoformates for the preparation of 8-unsubstituted-purines,formic acid still has a useful place in purine syntheses.

C . Cyclization Involving Reaction of a 5-AZO Group ( H 7 3 ) . . . . . . . . Syntheses from 5-Amino-4-oxopyrimidines ( M 6 ) . . . . . . . . . . . Syntheses from 4-Amino-5-unsubstituted-pyrimidines (ff78) . . . . . . . . Purines Derived from Pyrimidine-Containing Heterocycles (H8 I ) . . . . . . . A. 4-d]pyrimidines (H81) . . . . . . . . . . . . B. From Oxazolo [5,4-djpyrimidines (H82) . . . . . . . . . . . . F . From Thiadiazolo [3,4-dlpyrimidines (New) .

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