Download Elsevier’s Encyclopædia of Organic Chemistry: Series III: by F. Radt (auth.), F. Radt (eds.) PDF

By F. Radt (auth.), F. Radt (eds.)

When, many years in the past, the book of Elsevier's Encyclo­ pa:dia of natural Chemistry used to be suspended, it appeared fascinating to complete-on account of its monographic character-the steroid part based on the unique perception. One conside­ ration in favour thereof, between others, was once that the steroid component of Beilstein's Handbuch should not to be had for a few years yet to come, in order that additionally to these utilizing Beilstein the current booklet is a worthwhile assist in bridging the space. In view of the undiminished task during this specified box- both vital to chemists, bio­ chemists, and the clinical global - the wish that the of completion of this part will meet the desires of a large circle of readers ap­ pears tobe justified. Altogether 3 extra volumes are deliberate for the complement, the 1st of which, now offered, covers the steroid Oxo-com­ kilos, the Iiterature having been consulted as much as the tip of 1946 in conformity with the former volumes of the steroid complement. the place, although, very important additions and correc­ tions are involved, Iiterature as much as the latest date has been taken into consideration. In treating the subject material a similar prin­ ciples were as within the past volumes of this part. Editorship is still within the useful fingers of Dr. F. RADT, who has contributed a substantial share of the problem handled during this quantity. he's assisted by way of Dr. A. GEORG and Dr. DoRA STERN.

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02 mm. pressure (small yield); analogously, along with the acetate of L1 11 -pregnen-31X-ol-2o-one, from the 3-acetate 12-(anthraquinone-2-carboxylate) of the same diolone (small yicld) (1944 v. Euw). CO · CH 3 CiJ-J (III} -Pregnadien-20-one (III), C21 H 30 0. Properties and mode of formation have not been described. - Rns. May be converted into L1 4 -androsten-17-one and L1 5 -androsten-17-one, resp. (pp. ) by treatment of their oximes with p-toluenesulphonyl chloride in cold pyridine, followed by hydrolysis with dil.

1946 Shoppee, '}. Ch. Soc. 1946 1147, 1149. * Societe pour l'industrie chimique a Bale; Gesellschaft für chemische Industrie in Basel. DIAZOPREGNANONE 2224 s VoL. 14 s (14 p. II4) 3. DIAZO-MONOOXOSTEROIDS (CO IN SIDE CHAIN) 21-Diazo-LI 2-allopregnen-20-one C21 H 30 0N 2 . Crystals (ether-methanol), m. 140° cor. ; [cx]o + 178° (chloroform). - Fmn. From MIe -CO·CHN 2 ~ M ("I ~H~ Ll 2-

Nederland Nitrocellulose Norw. Pat. Nova Acta Regiae Soc. Sei. Upsaliensis Nuovo cimento Nutrition Abstr. & Revs. Nachrichten von der Gesellschaft der Wissenschaften zu Göttingen, mathematisch-physikalische Klasse Nachrichtenblatt für den deutschen Pflanzenschutzdienst Nature (London) La Nature Die Naturwissenschaften Naturwissenschaftliche Museumshefte Natuurwetenschappelijk Tijdschrift Nederlandsch Tijdschrift voor Geneeskunde Neues Repertorium für Pharmazie New Orleans Medical and Surgical Journal The New Zealand Journal of Science and Technology News Edition (American Chemical Society) Nieuw Tijdschrift voor de Pharmacie in Nederland Nitrocellulose Norwegian Patent Nova Acta Regiae Societatis Scientiarum Upsaliensis Nuovo cimento Nutrition Abstracts & Reviews Ötfentl.

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