The Chemistry of Synthetic DrugsLongmans, Green and Company, 1911 - 229 páginas |
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Página vii
... and to Mr. H. J. Page and Mr. E. de Barry Barnett for assistance in correcting the proofs . UNIVERSITY OF LONDON , UNIVERSITY COLLEGE , February , 1911 . 1 CONTENTS CHAPTER I INTRODUCTION - THEORIES OF THE ACTION PREFACE vii.
... and to Mr. H. J. Page and Mr. E. de Barry Barnett for assistance in correcting the proofs . UNIVERSITY OF LONDON , UNIVERSITY COLLEGE , February , 1911 . 1 CONTENTS CHAPTER I INTRODUCTION - THEORIES OF THE ACTION PREFACE vii.
Página ix
Percy May. CONTENTS CHAPTER I INTRODUCTION - THEORIES OF THE ACTION OF SYNTHETIC DRUGS CHAPTER II THE EFFECT OF VARIOUS ELEMENTS AND RADICLES Inorganic Elements · Radicles and Elements in Organic Compounds . CHAPTER III THE CHEMICAL ...
Percy May. CONTENTS CHAPTER I INTRODUCTION - THEORIES OF THE ACTION OF SYNTHETIC DRUGS CHAPTER II THE EFFECT OF VARIOUS ELEMENTS AND RADICLES Inorganic Elements · Radicles and Elements in Organic Compounds . CHAPTER III THE CHEMICAL ...
Página x
... CHAPTER XI OTHER ORGANIC ANTISEPTICS , EXCLUDING IODINE COMPOUNDS ( 1 ) Naphthalene , Pyridine , and Quinoline Derivatives ( 2 ) Formaldehyde ( 3 ) Tannic and Gallic Acids CHAPTER XII IODOFORM AND ITS COMPOUNDS • SUBSTITUTES - OTHER ...
... CHAPTER XI OTHER ORGANIC ANTISEPTICS , EXCLUDING IODINE COMPOUNDS ( 1 ) Naphthalene , Pyridine , and Quinoline Derivatives ( 2 ) Formaldehyde ( 3 ) Tannic and Gallic Acids CHAPTER XII IODOFORM AND ITS COMPOUNDS • SUBSTITUTES - OTHER ...
Página xiii
... ,. C , H ,. Groups such as benzyl , C , H ,. CH2- , obtained by removal of a hydrogen atom from the side - chain , must be regarded as mixed alkyl and aryl groups . xiii CHAPTER I INTRODUCTION - THE THEORY OF THE ACTION OF.
... ,. C , H ,. Groups such as benzyl , C , H ,. CH2- , obtained by removal of a hydrogen atom from the side - chain , must be regarded as mixed alkyl and aryl groups . xiii CHAPTER I INTRODUCTION - THE THEORY OF THE ACTION OF.
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Términos y frases comunes
acetyl acid group active adrenaline alcohol aldehyde aliphatic alkaline alkaloids alkyl groups amines amino group ANATOMY anesthetic aniline Annalen antimony antipyretic antiseptic aromatic arsenic atoms atoxyl atropine benzene by-effects carbon carboxyl CH.OH CH₂ CH2 CH2 CH₂O Chem chemical chloral chloride chloroform cocaine codeine compounds containing COOH Crown 8vo D.Sc derivatives drugs ecgonine entrance ester ether example formula guaiacol H₂C hydrogen hydrolyzed hydroxyl group hypnotic action Ibid Illustrations inert insoluble iodide iodine iodoform ketones large number less toxic medicine methyl groups methylamine MICHI molecule morphine mydriatic narcotic action narcotine NH.CO.CH NH₂ obtained OCH3 organism oxidized papaverine phenacetin phenetidine phenol physiol physiological action physiological effect piperidine poisonous potassium prepared Proc produced properties pyridine quinine radicles reduction resembles RSITY UNIV salicylic acid salol similar SITY sodium salt soluble in water solution substance sulphonic sulphuric acid synthesis synthetic therapeutic tissues tropine UNIV RSITY UNIV UNIVE yields он
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