Synthesis of O,O-diethyl arylthiophosphonate from O-Aryl-O,O-diethylthiophosphate

T. Dieng; A. Fraix; J.Y. Salaün; I. Dez; R.J.M. Klein Gebbink; G. van Koten; P.A. Jaffrès

Synthesis of O,O-diethyl arylthiophosphonate from O-Aryl-O,O-diethylthiophosphate

T. Dieng
, A. Fraix
, J.Y. Salaün
, I. Dez
, R.J.M. Klein Gebbink
, G. van Koten
, P.A. Jaffrès

Dept of Chemistry

extern

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

The synthesis of O,O-diethyl 2-hydroxyarylthiophosphonate is reported by using a [1,3]-rearrangement. This method is achieved in high yield from ortho-bromophenols derivatives by a two-step process

Original language	Undefined/Unknown
Pages (from-to)	3121-3124
Number of pages	5
Journal	Synlett
Volume	2008
Issue number	20
Publication status	Published - 2008

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Cite this

@article{905fcafa57f840e7899c591ad4f98c19,

title = "Synthesis of O,O-diethyl arylthiophosphonate from O-Aryl-O,O-diethylthiophosphate",

abstract = "The synthesis of O,O-diethyl 2-hydroxyarylthiophosphonate is reported by using a [1,3]-rearrangement. This method is achieved in high yield from ortho-bromophenols derivatives by a two-step process",

author = "T. Dieng and A. Fraix and J.Y. Sala{\"u}n and I. Dez and \{Klein Gebbink\}, R.J.M. and \{van Koten\}, G. and P.A. Jaffr{\`e}s",

year = "2008",

language = "Undefined/Unknown",

volume = "2008",

pages = "3121--3124",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "20",

}

TY - JOUR

T1 - Synthesis of O,O-diethyl arylthiophosphonate from O-Aryl-O,O-diethylthiophosphate

AU - Dieng, T.

AU - Fraix, A.

AU - Salaün, J.Y.

AU - Dez, I.

AU - Klein Gebbink, R.J.M.

AU - van Koten, G.

AU - Jaffrès, P.A.

PY - 2008

Y1 - 2008

N2 - The synthesis of O,O-diethyl 2-hydroxyarylthiophosphonate is reported by using a [1,3]-rearrangement. This method is achieved in high yield from ortho-bromophenols derivatives by a two-step process

AB - The synthesis of O,O-diethyl 2-hydroxyarylthiophosphonate is reported by using a [1,3]-rearrangement. This method is achieved in high yield from ortho-bromophenols derivatives by a two-step process

M3 - Article

SN - 0936-5214

VL - 2008

SP - 3121

EP - 3124

JO - Synlett

JF - Synlett

IS - 20

ER -