Controlled monohalogenation of phosphonates: A new route to pure α-monohalogenated diethyl benzylphosphonates
✍ Scribed by Bogdan Iorga; Frédéric Eymery; Philippe Savignac
- Book ID
- 104209243
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 981 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Starting from diethyl benzylphosphonates, a wide variety of diethyl ot-monofluoro, chloro, bromo and iodobenzylphosphonates have been obtained in pure form by a one-pot procedure. This high yielding method implies the intermediate protection of the benzyl anion with TMSC1 followed by halogenation with an electrophilic halogenating reagent.
📜 SIMILAR VOLUMES
## Abstract An efficient methodology for the synthesis of α‐aminophosphonates has been developed taking advantage of the __tert__‐butyldimethylsilyl triflate activated addition of diethyl phosphite to __N__‐benzyl nitrones derived from chiral α‐alkoxy and α‐(Boc‐amino) aldehydes. The stereoselectiv