New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles

Siva S. Panda; Peter J. Steel

doi:10.1016/j.tetlet.2014.07.057

New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles

Siva S. Panda
, Peter J. Steel

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

75 Scopus citations

Abstract

Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.

Original language	English (US)
Pages (from-to)	5898-5901
Number of pages	4
Journal	Tetrahedron Letters
Volume	55
Issue number	43
DOIs	https://doi.org/10.1016/j.tetlet.2014.07.057
State	Published - Oct 22 2014

Keywords

Benzotriazole
Conjugates
Methodology
Nucleophile
Phosphonylation

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

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10.1016/j.tetlet.2014.07.057

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@article{849bb40a88e84f0881b822c7b183ed9d,

title = "New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles",

abstract = "Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.",

keywords = "Benzotriazole, Conjugates, Methodology, Nucleophile, Phosphonylation",

author = "Panda, \{Siva S.\} and Steel, \{Peter J.\}",

note = "Funding Information: We thank the University of Florida and the Kenan Foundation and the Research Foundation-Flanders (FWO-Vlaanderen; fellowship to JCMM) for financial support. This paper was also funded in part by generous support from King Abdulaziz University , under grant No. ( D-006/431 ). The authors, therefore, acknowledge the technical and financial support of KAU. We also thank to Michael P. DesRosiers for his assistance. Publisher Copyright: {\textcopyright} 2014 Elsevier Ltd. All rights reserved.",

year = "2014",

month = oct,

day = "22",

doi = "10.1016/j.tetlet.2014.07.057",

language = "English (US)",

volume = "55",

pages = "5898--5901",

journal = "Tetrahedron Letters",

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publisher = "Elsevier Ltd",

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TY - JOUR

T1 - New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles

AU - Panda, Siva S.

AU - Steel, Peter J.

N1 - Funding Information: We thank the University of Florida and the Kenan Foundation and the Research Foundation-Flanders (FWO-Vlaanderen; fellowship to JCMM) for financial support. This paper was also funded in part by generous support from King Abdulaziz University , under grant No. ( D-006/431 ). The authors, therefore, acknowledge the technical and financial support of KAU. We also thank to Michael P. DesRosiers for his assistance. Publisher Copyright: © 2014 Elsevier Ltd. All rights reserved.

PY - 2014/10/22

Y1 - 2014/10/22

N2 - Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.

AB - Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields.

KW - Benzotriazole

KW - Conjugates

KW - Methodology

KW - Nucleophile

KW - Phosphonylation

UR - https://www.scopus.com/pages/publications/84907452285

UR - https://www.scopus.com/pages/publications/84907452285#tab=citedBy

U2 - 10.1016/j.tetlet.2014.07.057

DO - 10.1016/j.tetlet.2014.07.057

M3 - Article

AN - SCOPUS:84907452285

SN - 0040-4039

VL - 55

SP - 5898

EP - 5901

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 43

ER -

New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles

Abstract

Keywords

ASJC Scopus subject areas

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