1.

Record Nr.

UNISALENTO991004146359707536

Autore

García Márquez, Gabriel

Titolo

Relato de un naufrago ... / Gabriel García Márquez

Pubbl/distr/stampa

Barcelona : Tusquets, 1970

Descrizione fisica

88 p. : ill. ; 18 cm.

Collana

Cuadernos marginales ; 8

Disciplina

863

Lingua di pubblicazione

Spagnolo

Formato

Materiale a stampa

Livello bibliografico

Monografia

2.

Record Nr.

UNINA9910148953103321

Autore

Fraser George MacDonald

Titolo

Flashman in the Great Game (The Flashman Papers, Book 8)

Pubbl/distr/stampa

HarperCollins UK

ISBN

0-00-759350-3

Lingua di pubblicazione

Inglese

Formato

Musica

Livello bibliografico

Monografia

Sommario/riassunto

Harry Flashman: the unrepentant bully of Tom Brown's schooldays, now with a Victoria Cross, has three main talents - horsemanship, facility with foreign languages and fornication. A reluctant military hero, Flashman plays a key part in most of the defining military campaigns of the 19th century, despite trying his utmost to escape them all.What caused the Indian Mutiny? The greased cartridge, religious fanaticism, political blundering, yes - but one hitherto unsuspected factor is now



revealed to be the furtive figure who fled across India in 1857 with such frantic haste: Flashman.Plumbing new depths of anxious knavery in his role as secret agent extraordinaire, Flashman saw far more of the Great Mutiny than he wanted. How he survived Thugs and Tsarist agents, Eastern beauties and cabinet ministers and kept his skin intact is a mystery revealed here in this volume of The Flashman Papers.

3.

Record Nr.

UNINA9911018937503321

Autore

Smolin Edwin M

Titolo

s-Triazines and derivatives / / Edwin M. Smolin and Lorence Rapoport

Pubbl/distr/stampa

New York, : Interscience Publishers, 1959

ISBN

9786612301476

9781282301474

1282301470

9780470186626

0470186623

9780470188125

047018812X

Descrizione fisica

1 online resource (670 p.)

Collana

The chemistry of heterocyclic compounds ; ; 13

Altri autori (Persone)

RapoportLorence <1919-1999.>

Disciplina

547

547/.59/05

Soggetti

Triazines

Heterocyclic compounds

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Description based upon print version of record.

Nota di bibliografia

Includes bibliography.

Nota di contenuto

s-Triazines and Derivatives; Contents; Introduction; I. General; II. s-Triazine; 1. General; 2. Synthesis; 3. Reactions; A. Salt Formation; B. Hydrolysis; C. Reaction with Hydrogen Chloride; D. Reaction with Amines; E. Reaction with Halogens; F. Reaction with Sodamide; G. Hydrogenation; H. Friedel-Crafts Reaction of s-Triazine and Its Hydrochloride Derivatives; I. Grignard Reaction; I. Cyanuric Acid and Derivatives; I. Introduction; II. Cyanuric Acid; 1. Historical; 2. Physical Properties; A. General; B. Density; C. Thermal Properties; D. Heat of



Neutralization; E. Dissociation Constant

F. Percentage Dissociated at 35°G. Conductivity; H. Viscosity and Density of Solutions; I. Specific Heat; J. Magnetic Susceptibility; K. Raman, Infrared, and Ultraviolet Spectra; L. Polarographic Behavior; M. Crystallography and Miscellaneous Properties; 3. Synthesis and Occurrence; A. Natural Occurrence; B. From Cyanuric Halides; C. Polymerization of Cyanic Acid; D. From Urea and Urea Derivatives; E. From Uric Acid; F. From Allophanates and Carbamyl Chlorides; G. From Carbonyl Diurethane and Carbethoxybiuret; H. From Formamide Electrolytically; I. From Acetoxamide

J. From Carbaminothioglycolic Acid AnilideK. Miscellaneous Preparations; 4. Structure; 5. Salts of Cyanuric Acid; 6. Reactions of Cyanuric Acid; A. Hydrolysis; B. Reaction with Active Halogen Compounds; C. Thermal Action; D. Reaction with Ammonia; E. Esterification; F. Acetylation; G. Reaction with Fatty Acids; H. Reaction with α-Haloacids; I. Rearrangement .; 7. Applications of Cyanuric Acid; A. Physiological and Technical Significance; B. Melamine Formation; C. Rubber Manufacture; D. Resins; III. Cyanuric Halides; 1. Cyanuric Chloride; A. History; B. Physical Properties

C. Synthetic Methods(1) From Cyanogen Chloride; (2) From Hydrocyanic Acid; (3) From Cyanuric Acid; (4) Miscellaneous Methods; D. Structure; E. Reactions; (1) Hydrolysis and Alcoholysis; (2) Reaction with Hydroxy Compounds; (3) Reaction with Amino Compounds; (4) Reaction with Sulfhydryl Compounds; (5) Reaction with Salts of Hydrazoic Acid; (6) Reaction with Silver Nitrate; (7) Grignard Reaction; (8) Wurtz-Fittig Reaction; (9) Friedel-Crafts Reaction; (10) Reaction with Carboxylic Acids and Salts; (11) Reaction with Malonic Ester; (12) Reaction with Hydriodic Acid; (13) Reduction

(14) Reaction with BenzamideF. Physiological Properties; 2. Cyanuric Bromide; A. Synthesis; (1) Polymerization of Cyanogen Bromide; (2) From Bromine and Potassium Ferrocyanide; B. Reactions and Structure; (1) Hydrolysis; (2) Reaction with Amines; (3) With Acetic Acid; (4) Reaction with Urea; 3. Cyanuric Iodide; 4. Cyanuric Fluoride; 5. 2-Bromo-4,6-dichloro-s-triazine; 6. 2-Chloro-4,6-diiodo-s-triazine; IV. Cyanuric Acid Esters; 1. Alkyl Esters; A. Methyl Esters; (1) Trimethyl Ester; (2) Diethyl Ester; (3) Halomethoxy-s-triazines; (4) Mixed Methyl Esters; B. Ethyl Esters; (1) Triethyl Ester

(2) Dimethyl Ester

Sommario/riassunto

Chemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus.