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The institution of chemical engineers

Publisher
Wiley (John Wiley & Sons)
Year
1936
Weight
113 KB
Volume
55
Category
Article
ISSN
0368-4075

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โœฆ Synopsis

Further consideration of tho rcsults described in Part I (Callow and Rosenlicitn, J.C.S., 1033, 387)

indicates that ergosterol-D, forincd by thc iiiteraction of dihydroergostcrol and seleiiirim dioside, is t h o AO*s: I ( * l > : Z l * z ~ coiiipound, whilst tlic oxide formed a t the sniiic tiiiic is tlie 8 : 14-compound and yields the A718: 16 :ztlzz-co~iipoiiii(l, crgostcrol-B,, 011 decoinpositioii.

System of nuinbering steroitl compounds.

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con firincil in gcnernl Norrish nnd his c01Icngncs' estimates of thc contribiit.ions from tlic rcnctioii ZE,COlE, -> R! + 1j2 + CO. Tlic \~nliics intlicntc, liowcver, tlint, fission of nn nctivntcil niolcculc directly into a liy.drocnrboii, thus : RICOIE,\* -+ CO + RlR2, iiiiiy ~vcll plny an :ipprcc