𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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


A New and Expedient Diastereoselective S
✍ Carmela De Risi; Daniela Perrone; Alessandro Dondoni; Gian Piero Pollini; Valeri 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

## 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