Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions

S. J. Bent; M. F. Mahon; R. L. Webster

doi:10.1039/C5DT01312G

Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions

S. J. Bent, M. F. Mahon, R. L. Webster

Department of Chemistry

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

6 Citations (SciVal)

247 Downloads (Pure)

Abstract

We report a rare example of the malonamide functionality being used as a ligand in copper catalysis. We have ligated a homologous series of these O,O-chelating architectures to copper, investigated their structure and exploited them in azide–alkyne cycloaddition reactions for the step-growth synthesis of oligo(triazoles) and in the synthesis of small organic azoles.

Original language	English
Pages (from-to)	10253-10258
Number of pages	6
Journal	Dalton Transactions
Volume	44
Issue number	22
Early online date	5 May 2015
DOIs	https://doi.org/10.1039/C5DT01312G
Publication status	Published - 14 Jun 2015

Access to Document

10.1039/C5DT01312G

DT Art v1.8Accepted author manuscript, 575 KB

Cite this

@article{0773f4c57df845ccaee7036ca1bfb5bc,

title = "Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions",

abstract = "We report a rare example of the malonamide functionality being used as a ligand in copper catalysis. We have ligated a homologous series of these O,O-chelating architectures to copper, investigated their structure and exploited them in azide–alkyne cycloaddition reactions for the step-growth synthesis of oligo(triazoles) and in the synthesis of small organic azoles.",

author = "Bent, {S. J.} and Mahon, {M. F.} and Webster, {R. L.}",

year = "2015",

month = jun,

day = "14",

doi = "10.1039/C5DT01312G",

language = "English",

volume = "44",

pages = "10253--10258",

journal = "Dalton Transactions ",

issn = "1477-9226",

publisher = "Royal Society of Chemistry",

number = "22",

}

TY - JOUR

T1 - Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions

AU - Bent, S. J.

AU - Mahon, M. F.

AU - Webster, R. L.

PY - 2015/6/14

Y1 - 2015/6/14

N2 - We report a rare example of the malonamide functionality being used as a ligand in copper catalysis. We have ligated a homologous series of these O,O-chelating architectures to copper, investigated their structure and exploited them in azide–alkyne cycloaddition reactions for the step-growth synthesis of oligo(triazoles) and in the synthesis of small organic azoles.

AB - We report a rare example of the malonamide functionality being used as a ligand in copper catalysis. We have ligated a homologous series of these O,O-chelating architectures to copper, investigated their structure and exploited them in azide–alkyne cycloaddition reactions for the step-growth synthesis of oligo(triazoles) and in the synthesis of small organic azoles.

UR - http://dx.doi.org/10.1039/C5DT01312G

U2 - 10.1039/C5DT01312G

DO - 10.1039/C5DT01312G

M3 - Article

SN - 1477-9226

VL - 44

SP - 10253

EP - 10258

JO - Dalton Transactions

JF - Dalton Transactions

IS - 22

ER -

Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions

Abstract

Access to Document

Other files and links

Fingerprint

Cite this