Issue 85, 2014

Substituent controlled reactivity switch: selective synthesis of α-diazoalkylphosphonates or vinylphosphonates via nucleophilic substitution of alkyl bromides with Bestmann–Ohira reagent

Abstract

We report a substituent controlled nucleophilic displacement of alkyl bromides with Bestmann–Ohira reagent yielding either dimethyl diazoalkylphosphonates or (E)-vinylphosphonates. The dimethyl diazoalkylphosphonates could be readily converted into corresponding (E)-vinylphosphonates in the presence of Cu following nitrogen elimination in quantitative yields.

Graphical abstract: Substituent controlled reactivity switch: selective synthesis of α-diazoalkylphosphonates or vinylphosphonates via nucleophilic substitution of alkyl bromides with Bestmann–Ohira reagent

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2014
Accepted
03 Sep 2014
First published
12 Sep 2014

Chem. Commun., 2014,50, 12896-12898

Author version available

Substituent controlled reactivity switch: selective synthesis of α-diazoalkylphosphonates or vinylphosphonates via nucleophilic substitution of alkyl bromides with Bestmann–Ohira reagent

M. M. D. Pramanik, A. K. Chaturvedi and N. Rastogi, Chem. Commun., 2014, 50, 12896 DOI: 10.1039/C4CC05684A

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