Addition-elimination reactions from germanium heterocycles 1,3-diazolidines (X = Y = NMe). -Summary. The reactivity of X-Gerrna-l,3-diazolidines with unsaturated compounds such as heterocurnulenes (CSz, PhNCO, PhNCS) and with carbonyl compounds (aldehydes and ketones) has been investigated. Generall
Réactions d'addition-élimination à partir d'hétérocycles germaniés du type I. Cas des dioxolannes germaniés
✍ Scribed by Gabriel Dousse; Hélène Lavayssière; Jacques Satgé
- Book ID
- 102856480
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 962 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Addition‐elimination reactions from germanium heterocycles I. Germadioxolanes (XYO)
The reactivity of 2‐germa‐1,3‐dioxolanes is studied with unsaturated compounds such as carbonyl compounds (aldehydes and ketones) or heterocumulenes (PhNCO, PhNCS). The formation of mono‐ and di‐insertion derivatives is observed. The structure of these adducts is established and their decomposition process, at atmospheric pressure or at high pressure, is precised.
The mechanism of these addition‐elimination reactions is established from 4,5‐disubstitued germadioxolanes. The reaction takes place under steric control. The consecutive elimination reaction proceeds by a mechanism of intramolecular nucleophilic substitution.
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## Addition-elimination reactions from germanium heterocycles RzGe . 111. 2,2-Diethyl-2-germa-1,3-oxazolidines (R = Et; X = 0; Y = NH,NMe). -Summary. The reactions of Z,Z-diethyl-Z-germa-l, 3-oxazolidines with heterocumulenes (PhNCO, PhNCS, CSz, COz, CHz=C=O) and carbonyl compounds (aldehydes and