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

Siva S. Panda, Peter J. Steel

Research output: Contribution to journalArticle

31 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)5898-5901
Number of pages4
JournalTetrahedron Letters
Volume55
Issue number43
DOIs
StatePublished - Oct 22 2014

Fingerprint

Nucleophiles
benzotriazole

Keywords

  • Benzotriazole
  • Conjugates
  • Methodology
  • Nucleophile
  • Phosphonylation

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles. / Panda, Siva S.; Steel, Peter J.

In: Tetrahedron Letters, Vol. 55, No. 43, 22.10.2014, p. 5898-5901.

Research output: Contribution to journalArticle

@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.}",
year = "2014",
month = "10",
day = "22",
doi = "10.1016/j.tetlet.2014.07.057",
language = "English (US)",
volume = "55",
pages = "5898--5901",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "43",

}

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.

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 - http://www.scopus.com/inward/record.url?scp=84907452285&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84907452285&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2014.07.057

DO - 10.1016/j.tetlet.2014.07.057

M3 - Article

AN - SCOPUS:84907452285

VL - 55

SP - 5898

EP - 5901

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 43

ER -