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High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts

Synthetic access to poly(indazolyl)methanes has limited their study despite their structural similarity to the highly investigated chelating poly(pyrazolyl)methanes and their potentially important indazole moiety. Herein is presented a high yielding, one-pot synthesis for the 3d-metal catalyzed form...

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Autores principales: Lind, Natalie M., Joe, Natalie S., Newell, Brian S., Morris, Aimee M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779710/
https://www.ncbi.nlm.nih.gov/pubmed/35072056
http://dx.doi.org/10.3390/reactions3010005
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author Lind, Natalie M.
Joe, Natalie S.
Newell, Brian S.
Morris, Aimee M.
author_facet Lind, Natalie M.
Joe, Natalie S.
Newell, Brian S.
Morris, Aimee M.
author_sort Lind, Natalie M.
collection PubMed
description Synthetic access to poly(indazolyl)methanes has limited their study despite their structural similarity to the highly investigated chelating poly(pyrazolyl)methanes and their potentially important indazole moiety. Herein is presented a high yielding, one-pot synthesis for the 3d-metal catalyzed formation of bis(1H-indazol-1-yl)methane from 1H-indazole utilizing dimethylsulfoxide as the methylene source. Complete characterization of bis(1H-indazol-1-yl)methane is given with (1)H and (13)C NMR, UV/Vis, FTIR, high resolution mass spectrometry and for the first time, single crystal X-ray diffraction. This simple, inexpensive pathway to yield exclusively bis(1H-indazol-1-yl)methane provides synthetic access to further investigate the coordination and potential applications of the family of bis(indazolyl)methanes.
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spelling pubmed-87797102022-03-01 High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts Lind, Natalie M. Joe, Natalie S. Newell, Brian S. Morris, Aimee M. Reactions (Basel) Article Synthetic access to poly(indazolyl)methanes has limited their study despite their structural similarity to the highly investigated chelating poly(pyrazolyl)methanes and their potentially important indazole moiety. Herein is presented a high yielding, one-pot synthesis for the 3d-metal catalyzed formation of bis(1H-indazol-1-yl)methane from 1H-indazole utilizing dimethylsulfoxide as the methylene source. Complete characterization of bis(1H-indazol-1-yl)methane is given with (1)H and (13)C NMR, UV/Vis, FTIR, high resolution mass spectrometry and for the first time, single crystal X-ray diffraction. This simple, inexpensive pathway to yield exclusively bis(1H-indazol-1-yl)methane provides synthetic access to further investigate the coordination and potential applications of the family of bis(indazolyl)methanes. 2022-03 2022-01-04 /pmc/articles/PMC8779710/ /pubmed/35072056 http://dx.doi.org/10.3390/reactions3010005 Text en https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lind, Natalie M.
Joe, Natalie S.
Newell, Brian S.
Morris, Aimee M.
High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title_full High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title_fullStr High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title_full_unstemmed High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title_short High Yielding, One-Pot Synthesis of Bis(1H-indazol-1-yl)methane Catalyzed by 3d-Metal Salts
title_sort high yielding, one-pot synthesis of bis(1h-indazol-1-yl)methane catalyzed by 3d-metal salts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779710/
https://www.ncbi.nlm.nih.gov/pubmed/35072056
http://dx.doi.org/10.3390/reactions3010005
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