Both compounds (I\') and (V) hitvc bccn synthesised, ond thc identity of tlic dcgradntion and synthetical products, which arc liquids, has bccn cstablishcd by comparison of certain dcrivntivcs. Prof. C. H. Ingold said that Dr. King's hypothesis t1i:it tlic isoquinoliiic iiiid bcuzciic I' linlocs " o
The institution of chemical engineers
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1930
- Weight
- 141 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0368-4075
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โฆ Synopsis
Tlic snmc prc1)nrntion can bc equally wcll carried out by using glucosc ns the sq1)stratc.
๐ SIMILAR VOLUMES
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
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 tiii