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

Chemistry and Physics

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

43 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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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.}",

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AU - Panda, Siva S.

AU - Steel, Peter J.

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KW - Conjugates

KW - Methodology

KW - Nucleophile

KW - Phosphonylation

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