Carbamoylphosphonates part 7. An efficient method for the synthesis of hindered carbamoylphosphonates using 4-nitrophenoxycarbonylphosphonate diesters

Irena Beylis; Julia Frant; Naama Mussai; Reuven Reich; Eli Breuer

doi:10.1016/j.tetlet.2008.03.036

Carbamoylphosphonates part 7. An efficient method for the synthesis of hindered carbamoylphosphonates using 4-nitrophenoxycarbonylphosphonate diesters

Irena Beylis, Julia Frant, Naama Mussai, Reuven Reich, Eli Breuer^*

^*Corresponding author for this work

School of Pharmacy

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

6 Scopus citations

Abstract

Hindered primary amines that resist other reagents can be converted to carbamoylphosphonates by means of 4-nitrophenoxycarbonylphosphonate diesters in high yields and under mild conditions.

Original language	English
Pages (from-to)	2875-2877
Number of pages	3
Journal	Tetrahedron Letters
Volume	49
Issue number	18
DOIs	https://doi.org/10.1016/j.tetlet.2008.03.036
State	Published - 28 Apr 2008

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10.1016/j.tetlet.2008.03.036

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title = "Carbamoylphosphonates part 7. An efficient method for the synthesis of hindered carbamoylphosphonates using 4-nitrophenoxycarbonylphosphonate diesters",

abstract = "Hindered primary amines that resist other reagents can be converted to carbamoylphosphonates by means of 4-nitrophenoxycarbonylphosphonate diesters in high yields and under mild conditions.",

author = "Irena Beylis and Julia Frant and Naama Mussai and Reuven Reich and Eli Breuer",

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AU - Beylis, Irena

AU - Frant, Julia

AU - Mussai, Naama

AU - Reich, Reuven

AU - Breuer, Eli

PY - 2008/4/28

Y1 - 2008/4/28

N2 - Hindered primary amines that resist other reagents can be converted to carbamoylphosphonates by means of 4-nitrophenoxycarbonylphosphonate diesters in high yields and under mild conditions.

AB - Hindered primary amines that resist other reagents can be converted to carbamoylphosphonates by means of 4-nitrophenoxycarbonylphosphonate diesters in high yields and under mild conditions.

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DO - 10.1016/j.tetlet.2008.03.036

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AN - SCOPUS:41349111232

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VL - 49

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 18

ER -

Carbamoylphosphonates part 7. An efficient method for the synthesis of hindered carbamoylphosphonates using 4-nitrophenoxycarbonylphosphonate diesters

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