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

Access to Document

10.1016/j.tetlet.2008.03.036

Cite this

@article{95db6b87ccb148e29e87b6533203e68c,

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",

year = "2008",

month = apr,

day = "28",

doi = "10.1016/j.tetlet.2008.03.036",

language = "אנגלית",

volume = "49",

pages = "2875--2877",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "18",

}

TY - JOUR

T1 - Carbamoylphosphonates part 7. An efficient method for the synthesis of hindered carbamoylphosphonates using 4-nitrophenoxycarbonylphosphonate diesters

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.

UR - https://www.scopus.com/pages/publications/41349111232

U2 - 10.1016/j.tetlet.2008.03.036

DO - 10.1016/j.tetlet.2008.03.036

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:41349111232

SN - 0040-4039

VL - 49

SP - 2875

EP - 2877

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

Abstract

Access to Document

Other files and links

Fingerprint

Cite this