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
✦ LIBER ✦
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
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2010
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John Wiley and Sons
⚖ 34 KB