A simple route to N-acylaminophosphonoacetates (N-protected phosphonylglycine esters).

L. Ferris; David Haigh; C.J. Moody

A simple route to N-acylaminophosphonoacetates (N-protected phosphonylglycine esters).

L. Ferris, David Haigh, C.J. Moody

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

Abstract

Rhodium(II) acetate catalyzed reaction of tri-Et diazophosphonoacetate with amides, carbamates or ureas gives a range of N-acyl phosphonylglycine derivs. by N-H insertion reaction of the intermediate rhodium carbenoid.

Original language	English
Pages (from-to)	921-922
Number of pages	2
Journal	Synlett
Volume	-
Publication status	Published - 1995

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title = "A simple route to N-acylaminophosphonoacetates (N-protected phosphonylglycine esters).",

abstract = "Rhodium(II) acetate catalyzed reaction of tri-Et diazophosphonoacetate with amides, carbamates or ureas gives a range of N-acyl phosphonylglycine derivs. by N-H insertion reaction of the intermediate rhodium carbenoid.",

author = "L. Ferris and David Haigh and C.J. Moody",

year = "1995",

language = "English",

volume = "-",

pages = "921--922",

journal = "Synlett",

issn = "0936-5214",

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T1 - A simple route to N-acylaminophosphonoacetates (N-protected phosphonylglycine esters).

AU - Ferris, L.

AU - Haigh, David

AU - Moody, C.J.

PY - 1995

Y1 - 1995

N2 - Rhodium(II) acetate catalyzed reaction of tri-Et diazophosphonoacetate with amides, carbamates or ureas gives a range of N-acyl phosphonylglycine derivs. by N-H insertion reaction of the intermediate rhodium carbenoid.

AB - Rhodium(II) acetate catalyzed reaction of tri-Et diazophosphonoacetate with amides, carbamates or ureas gives a range of N-acyl phosphonylglycine derivs. by N-H insertion reaction of the intermediate rhodium carbenoid.

M3 - Article

VL - -

SP - 921

EP - 922

JO - Synlett

JF - Synlett

SN - 0936-5214

ER -

A simple route to N-acylaminophosphonoacetates (N-protected phosphonylglycine esters).

Abstract

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