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Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines

A novel method for the preparation of hitherto unknown symmetrical bis(2-halo-3-pyridyl) dichalcogenides (E = S, Se and Te) by the oxidation of intermediate 2-halo-3-pyridyl chalcogenolate, prepared by lithiation of 2-halo pyridines using lithium diisopropylamine is being reported. All the newly syn...

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Autores principales: Bhasin, K. K., Singh, Neelam, Doomra, Shivani, Arora, Ekta, Ram, Ganga, Singh, Sukhjinder, Nagpal, Yogesh, Mehta, S. K., Klapotke, T. M.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885866/
https://www.ncbi.nlm.nih.gov/pubmed/17611613
http://dx.doi.org/10.1155/2007/69263
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author Bhasin, K. K.
Singh, Neelam
Doomra, Shivani
Arora, Ekta
Ram, Ganga
Singh, Sukhjinder
Nagpal, Yogesh
Mehta, S. K.
Klapotke, T. M.
author_facet Bhasin, K. K.
Singh, Neelam
Doomra, Shivani
Arora, Ekta
Ram, Ganga
Singh, Sukhjinder
Nagpal, Yogesh
Mehta, S. K.
Klapotke, T. M.
author_sort Bhasin, K. K.
collection PubMed
description A novel method for the preparation of hitherto unknown symmetrical bis(2-halo-3-pyridyl) dichalcogenides (E = S, Se and Te) by the oxidation of intermediate 2-halo-3-pyridyl chalcogenolate, prepared by lithiation of 2-halo pyridines using lithium diisopropylamine is being reported. All the newly synthesized compounds have been characterized through elemental analysis employing various spectroscopic techniques, namely, NMR ((1)H, (13)C, (77)Se), infrared, mass spectrometry, and X-ray crystal structures in representative cases.
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spelling pubmed-18858662007-07-03 Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines Bhasin, K. K. Singh, Neelam Doomra, Shivani Arora, Ekta Ram, Ganga Singh, Sukhjinder Nagpal, Yogesh Mehta, S. K. Klapotke, T. M. Bioinorg Chem Appl Research Article A novel method for the preparation of hitherto unknown symmetrical bis(2-halo-3-pyridyl) dichalcogenides (E = S, Se and Te) by the oxidation of intermediate 2-halo-3-pyridyl chalcogenolate, prepared by lithiation of 2-halo pyridines using lithium diisopropylamine is being reported. All the newly synthesized compounds have been characterized through elemental analysis employing various spectroscopic techniques, namely, NMR ((1)H, (13)C, (77)Se), infrared, mass spectrometry, and X-ray crystal structures in representative cases. Hindawi Publishing Corporation 2007 2007-03-25 /pmc/articles/PMC1885866/ /pubmed/17611613 http://dx.doi.org/10.1155/2007/69263 Text en Copyright © 2007 K. K. Bhasin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bhasin, K. K.
Singh, Neelam
Doomra, Shivani
Arora, Ekta
Ram, Ganga
Singh, Sukhjinder
Nagpal, Yogesh
Mehta, S. K.
Klapotke, T. M.
Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title_full Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title_fullStr Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title_full_unstemmed Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title_short Regioselective Synthesis of Bis(2-halo-3-pyridyl) Dichalcogenides (E = S, Se and Te): Directed Ortho-Lithiation of 2-halopyridines
title_sort regioselective synthesis of bis(2-halo-3-pyridyl) dichalcogenides (e = s, se and te): directed ortho-lithiation of 2-halopyridines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885866/
https://www.ncbi.nlm.nih.gov/pubmed/17611613
http://dx.doi.org/10.1155/2007/69263
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