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Condensation of α-hydroxy ketones with phosphorus ylides: A convenient synthesis of linear heterocyclic formation

✍ Scribed by Wafaa M. Abdou; Yehia O. El-Khoshnieh; Azza A. Kamel


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
221 KB
Volume
10
Category
Article
ISSN
1042-7163

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✦ Synopsis


Reaction of ␣-hydroxy ketones, furoin (1a) and/or benzoin (1b), with an appropriate phosphorus ylide (6a-d) provides access to new alkenes E-8a-d, 15, 16 and/or furan derivatives 11a,b and 21. Furthermore, reaction of 1a,b with arylidenephosphorane 7 led to the formation of the respective dioxolo compound 22a,b.


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ChemInform Abstract: Condensation of α-H
✍ Wafaa M. Abdou; Yehia O. El-Khoshnieh; Azza A. Kamel 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB

Condensation of α-Hydroxy Ketones with Phosphorus Ylides: A Convenient Synthesis of Linear Heterocyclic Derivatives. -Depending on the electronic nature of substituents in the α-position of the methylenephosphorane and the reaction conditions, reaction of α-hydroxy ketones (I) with phosphorous ylide