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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/1951/volume_16
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_7/m/print http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_7/m/web
issue	7
is Is Part Of of	The Synthesis and Properties of some Alkyliodophenols Synthesis of Disecondary Amines; N,N'-Diphenyl-α, ω-Diaminoalkanes The Preparation of Diamino Acids via the Schmidt Reaction Attempted Syntheses of Pelletierine Exchange Reactions of α-Halogenated Pyridines Studies in the Juglone Series. III. Addition Reactions Steric Effects in Complex Compound formation Reaction of Acetyl Bromide and Acetyl Chloride with Urethans Isobenzopyrylium Salts. II. 1,3-Diphenyl-2-Benzopyrylium Salts Stearamidomethyl Ethers Dimeric Propenyl Phenol Ethers. XIII. on Metanethole and its Teralin Isomers Δ5, 7-Steroids. VII. The Conversion of Δ5, 7- to Δ5, 7, 9-Steroidal Hormones 7-Aminosteroids Structure Studies in the Morphine Series. Degradation of Dihydrothebaine to a Dimethoxytrialkyltetrahydronaphthalene Investigations on Steroids. XIV. Studies in the Series of the Adrenal Cortical Hormones: Dehydration of 6β,21-Diacetoxyallopregnane-5-OL-3, 20-Dione Branched-Chain Fatty Acids. XVII. Synthesis of two Trimethylalkanoic Acids. Certain Relationships of Boiling Point and Index of Refraction to Structure Branched-Chain Fatty Acids. XVIII. Ultraviolet Absorption Sepctra of Saturated Branched-Chain Acids Sulfonal Analogs Derived from Tetrahydrothiapyran Studies in Silico-Organic Compounds: XVI. Reactions of Alkyl Thioethers of Silicon with Acetic Anhydride and with Benzoyl Chloride The Synthesis of Compounds for the Chemotherapy of Tuberculosis. I. Heterocyclic Thiosemicarbazide Derivatives Reinvestigation of Alloxantin and Dialuric Acid Studies in Silico-Organic Compounds: XVII. The Action of Bromine on Alkyl Thioethers of Silicon Studies on Condensed Pyrimidine Systems. VIII (1). The 5,6-Dihydrofuro[2,3-d]Pyrimidine Ring System Δ5, 7-Steroids. VI. The Preparation of Δ5, 7-Steroidal Hormones

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