Schiff Bases: A Short Survey on an Evergreen Chemistry Tool

The review reports a short biography of the Italian naturalized chemist Hugo Schiff and an outline on the synthesis and use of his most popular discovery: the imines, very well known and popular as Schiff Bases. Recent developments on their “metallo-imines” variants have been described. The applicat...

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Detalles Bibliográficos
Autores principales: Qin, Wenling, Long, Sha, Panunzio, Mauro, Biondi, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270622/
https://www.ncbi.nlm.nih.gov/pubmed/24108395
http://dx.doi.org/10.3390/molecules181012264
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author Qin, Wenling
Long, Sha
Panunzio, Mauro
Biondi, Stefano
author_facet Qin, Wenling
Long, Sha
Panunzio, Mauro
Biondi, Stefano
author_sort Qin, Wenling
collection PubMed
description The review reports a short biography of the Italian naturalized chemist Hugo Schiff and an outline on the synthesis and use of his most popular discovery: the imines, very well known and popular as Schiff Bases. Recent developments on their “metallo-imines” variants have been described. The applications of Schiff bases in organic synthesis as partner in Staudinger and hetero Diels-Alder reactions, as “privileged” ligands in the organometallic complexes and as biological active Schiff intermediates/targets have been reported as well.
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spelling pubmed-62706222018-12-18 Schiff Bases: A Short Survey on an Evergreen Chemistry Tool Qin, Wenling Long, Sha Panunzio, Mauro Biondi, Stefano Molecules Review The review reports a short biography of the Italian naturalized chemist Hugo Schiff and an outline on the synthesis and use of his most popular discovery: the imines, very well known and popular as Schiff Bases. Recent developments on their “metallo-imines” variants have been described. The applications of Schiff bases in organic synthesis as partner in Staudinger and hetero Diels-Alder reactions, as “privileged” ligands in the organometallic complexes and as biological active Schiff intermediates/targets have been reported as well. MDPI 2013-10-08 /pmc/articles/PMC6270622/ /pubmed/24108395 http://dx.doi.org/10.3390/molecules181012264 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Qin, Wenling
Long, Sha
Panunzio, Mauro
Biondi, Stefano
Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title_full Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title_fullStr Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title_full_unstemmed Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title_short Schiff Bases: A Short Survey on an Evergreen Chemistry Tool
title_sort schiff bases: a short survey on an evergreen chemistry tool
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270622/
https://www.ncbi.nlm.nih.gov/pubmed/24108395
http://dx.doi.org/10.3390/molecules181012264
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AT biondistefano schiffbasesashortsurveyonanevergreenchemistrytool

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