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Photoisomerisierung von o-Di-isobutenylbenzol

✍ Scribed by L. Ulrich; H.-J. Hansen; H. Schmid


Publisher
John Wiley and Sons
Year
1970
Tongue
German
Weight
578 KB
Volume
53
Category
Article
ISSN
0018-019X

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✦ Synopsis


Si l'on met en suspension 100 mg de ce produit dans 100 ml d'acide acktique, ajoute 5 g de Na,Cr,O,, 2H,O et chauffe 4 h 2 reflux, on obtient, aprks avoir trait6 par l'eau, isole le pr6cipitC par centrifugation, s6ch6 et lave & 1'0-dichlorobenzhe bouillant, 97 mg (93,574) de bltonnets vert gris2tre ayant toutes les propriCt6s de la tricetone XIX.

Ce travail a b6nBfici6 de l'aide du Fonds national suisse de la recherche scientifique, auquel nous exprimons notre gratitude. intermediate state the acetate ion (and not pyridine, for steric reasons) attacks the carbon of the carbonyl function of the conjugate acid with the acetylium cation to yield 1,l-diacetoxy-2,2,2trichloro-ethane.

These two reactions occur only with aldehydes whose carbonyl is very electrophilic, and seem t o be a possible way to point out the presence of an acylium cation in pyridine medium.

Dans certaines circonstances, les condensations acyloiniques peuvent avoir lieu en milieu acide: Hensel [l] a montrC que le pyridinecarbaldChyde-2 se transforme


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Photochemische Reaktionen. 76.Mitteilung
✍ Peter Gull; Yoshihisa Saito; Hansuli Wehrli; Oskar Jeger 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 German ⚖ 701 KB

## Abstract The UV.‐isomerisation of 11‐oxo‐14β,17α‐pregnane **9** to the 11,19‐cyclo‐derivative **11** is described. In addition the Pb(OAc)~4~‐fragmentation of photoproduct **11** was investigated. **11** yielded besides the expected 11‐oxo‐19‐hydroxy‐pregnane **18** the novel 9,11‐seco‐11,19‐cyc