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Oxidative carbon-carbon bond cleavage of a α-hydroxy ketone by a functional model of 2,4'-dihydroxyacetophenone dioxygenase.

Bond cleavage: An iron(II)-[alpha]-hydroxy ketone complex of a facial tridentate nitrogen donor ligand undergoes a C--C bond cleavage reaction in the presence of dioxygen to form two equivalents of carboxylic acids. This reaction is a functional model of 2,4'-dihydroxyacetophenone dioxygenase.

Journal Title: Angewandte Chemie (International ed. in English) June 18, 2012, Vol.51(25), pp.6195-6199
Main Author: Paria, Sayantan
Other Authors: Halder, Partha , Paine, Tapan Kanti
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1521-3773 ; DOI: 10.1002/anie.201201825
Link: http://search.proquest.com/docview/1020509937/?pq-origsite=primo
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recordid: proquest1020509937
title: Oxidative carbon-carbon bond cleavage of a α-hydroxy ketone by a functional model of 2,4'-dihydroxyacetophenone dioxygenase.
format: Article
creator:
  • Paria, Sayantan
  • Halder, Partha
  • Paine, Tapan Kanti
subjects:
  • Dioxygenases–Chemistry
  • Ketones–Chemistry
  • Molecular Structure–Chemistry
  • Organometallic Compounds–Chemistry
  • Oxidation-Reduction–Chemistry
  • Ketones
  • Organometallic Compounds
  • Dioxygenases
  • 2,4'-Dihydroxyacetophenone Dioxygenase
ispartof: Angewandte Chemie (International ed. in English), June 18, 2012, Vol.51(25), pp.6195-6199
description: Bond cleavage: An iron(II)-[alpha]-hydroxy ketone complex of a facial tridentate nitrogen donor ligand undergoes a C--C bond cleavage reaction in the presence of dioxygen to form two equivalents of carboxylic acids. This reaction is a functional model of 2,4'-dihydroxyacetophenone dioxygenase.
language: eng
source:
identifier: E-ISSN: 1521-3773 ; DOI: 10.1002/anie.201201825
fulltext: fulltext
issn:
  • 15213773
  • 1521-3773
url: Link


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titleOxidative carbon-carbon bond cleavage of a α-hydroxy ketone by a functional model of 2,4'-dihydroxyacetophenone dioxygenase.
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subjectDioxygenases–Chemistry ; Ketones–Chemistry ; Molecular Structure–Chemistry ; Organometallic Compounds–Chemistry ; Oxidation-Reduction–Chemistry ; Ketones ; Organometallic Compounds ; Dioxygenases ; 2,4'-Dihydroxyacetophenone Dioxygenase
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descriptionBond cleavage: An iron(II)-[alpha]-hydroxy ketone complex of a facial tridentate nitrogen donor ligand undergoes a C--C bond cleavage reaction in the presence of dioxygen to form two equivalents of carboxylic acids. This reaction is a functional model of 2,4'-dihydroxyacetophenone dioxygenase.
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